Open Access

Microglia immunophenotyping in gliomas

  • Authors:
    • Laura Annovazzi
    • Marta Mellai
    • Enrica Bovio
    • Samanta Mazzetti
    • Bianca Pollo
    • Davide Schiffer
  • View Affiliations

  • Published online on: November 9, 2017
  • Pages:998-1006
  • Copyright: © Annovazzi et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Microglia, once assimilated to peripheral macrophages, in gliomas has long been discussed and currently it is hypothesized to play a pro‑tumor role in tumor progression. Uncertain between M1 and M2 polarization, it exchanges signals with glioma cells to create an immunosuppressive microenvironment and stimulates cell proliferation and migration. Four antibodies are currently used for microglia/macrophage identification in tissues that exhibit different cell forms and cell localization. The aim of the present work was to describe the distribution of the different cell forms and to deduce their significance on the basis of what is known on their function from the literature. Normal resting microglia, reactive microglia, intermediate and bumpy forms and macrophage‑like cells can be distinguished by Iba1, CD68, CD16 and CD163 and further categorized by CD11b, CD45, c‑MAF and CD98. The number of microglia/macrophages strongly increased from normal cortex and white matter to infiltrating and solid tumors. The ramified microglia accumulated in infiltration areas of both high‑ and low‑grade gliomas, when hypertrophy and hyperplasia occur. In solid tumors, intermediate and bumpy forms prevailed and there is a large increase of macrophage‑like cells in glioblastoma. The total number of microglia cells did not vary among the three grades of malignancy, but macrophage‑like cells definitely prevailed in high‑grade gliomas and frequently expressed CD45 and c‑MAF. CD98+ cells were present. Microglia favors tumor progression, but many aspects suggest that the phagocytosing function is maintained. CD98+ cells can be the product of fusion, but also of phagocytosis. Microglia correlated with poorer survival in glioblastoma, when considering CD163+ cells, whereas it did not change prognosis in isocitrate dehydrogenase‑mutant low grade gliomas.


Microglia has been categorized as quiescent ramified microglia with small round cells and numerous branching processes, ameboid or reactive microglia devoid of branching processes, macrophages and perivascular microglia (1). They can be intrinsic to the central nervous system (CNS) as resident microglia, or blood-borne from the monocytic phagocyting system of the blood. Both derive from the yolk sac, the resident microglia earlier and later the cells destined to bone marrow for hematopoiesis and migrating to the CNS crossing the blood-brain barrier (BBB) in case of lesions.

In normal CNS, resident microglia is 5–10% of cells (2,3). Microglia/macrophages increase in low-grade gliomas (LGG) (4), especially in pilocytic astrocytomas (5), and progressively with the glioma grades (6), reaching 30% of cells in high grade gliomas (HGG), closely correlating with vascular density (711), developing around and inside the tumors and clustering around vessels and necroses.

Contrary to what is known from other CNS diseases and from microglia assimilation to peripheral macrophages, glioma-associated M/M (GAMs) are today prevailingly interpreted as favoring glioma cell migration and growth (1215). GAM polarization into the two functional profiles M1 (classically activated, pro-inflammatory) and M2 (alternatively activated, immunosuppressive) has long been discussed (12,1319). Recently, GAMs have been shown to overlap only partial with the M1 and M2 phenotypes (20). Glioma cells would establish an immunosuppressive tumor environment, promoting GAM recruitment and proliferation, polarizing them toward the M2 phenotype and remaining unaffected by their phagocyting and anti-tumorigenic functions (16,1929). In this way they would be ‘friends’ and not ‘foes’ to gliomas (16,30). GAMs are recruited by glioma cells through chemoattractant factors and, in turn, they stimulate tumor growth (26,31,32). Both glioma cells and GAMs promote angiogenesis (33,34).

In tissue, four antibodies are currently used to demonstrate GAMs, i.e., allograft inflammatory factor 1 (Iba1), CD16, CD68, and CD163. They reveal different antigens with different final reaction products (FRP) and with different localization in the cells: In cytoplasms for Iba1, in lysosomes for CD68 and on cell membranes for CD16 and CD163. Various GAM forms can be demonstrated, going from ramified microglia to granular macrophage-like cells, which correspond to different antigen expression. Given the uncertainties still existing on the significance of GAMs, one wonders to which stimuli so various cell forms and immunohistochemical behaviors respond in the different tumor districts. The aim of this work is to clarify their functional significance after the systematic study of a broad series of human gliomas and to interpret them on the basis of the information available on their functions.

Materials and methods

Brain tumor specimens

The study has been carried out on 98 adult glioma specimens from our archive and operated on at different Neurosurgery Units of the Piedmont Region and at the Istituto Neurologico ‘Carlo Besta’ IRCCS Foundation, Milan, Italy. The series was composed of 3 pilocytic astrocytomas, 20 diffuse astrocytomas (16 isocitrate dehydrogenase (IDH)-mutant and 4 IDH-wild-type), 4 anaplastic astrocytomas (1 IDH-mutant and 3 IDH-wild-type), 26 oligodendrogliomas (20 IDH-mutant and 1p/19q-codeleted and 6 not otherwise specified (NOS)), 10 anaplastic oligodendrogliomas (6 IDH-mutant and 1p/19q-codeleted and 4 NOS) and 35 glioblastomas (GBs), IDH-wild-type. The histological diagnosis was made according to the current World Health Organization (WHO) guidelines (35). As controls, 10 tumor-free tissue samples were used. Surgical tumor samples were formalin fixed, paraffin embedded (FFPE) and cut in 5 µm-thick sections. The study was in compliance with the local institutional review board and Committee on Human Research and with the ethical human subject principles of the World Medical Association Declaration of Helsinki Research. Written informed consent of patients was obtained after the Ethics Committee approval.

Immunohistochemistry (IHC)

Beside haematoxylin and eosin (H&E) staining, immunohistochemical analyses were performed using a Ventana Full BenchMark® XT automated immunostainer (Ventana Medical Systems Inc., Tucson, AZ, USA) and the UltraView™ Universal DAB Detection Kit (Ventana Medical Systems Inc.) as detection system. Heat-induced epitope retrieval (HIER) was performed in Tris-EDTA, pH 8. Primary antibodies are listed in Table I. Double immunostainings for c-MAF/CD68, c-MAF/CD163, Iba1/CD34 and CD68/CD34 were performed with the ultraView™ Universal Alkaline Phosphatase Red Detection Kit (Ventana). Negative controls were obtained by omitting the primary antibodies. Observations were made on a Zeiss Axioskop fluorescence microscope (Carl Zeiss, Oberkochen, Germany) equipped with an AxioCam5 MR5c and coupled to an Imaging system (AxioVision Release 4.5; Carl Zeiss).

Table I.

List of primary antibodies used for immunohistochemistry.

Table I.

List of primary antibodies used for immunohistochemistry.

Antibody (Clone)SourceDilutionCodeManufacturer
Ki-67 (MIB-1)Mouse1:100M7240Dako
Iba1Rabbit1:500019–19741Wako Chemicals
CD68 (KP-1)MousePre-diluted790–2931Ventana
CD16 (SP175)RabbitPre-diluted760–4863Ventana
c-MAF (M-153)Rabbit1:50sc-7866Santa Cruz Biotech.
CD45 (LCA)MousePre-diluted760–2505Ventana
Molecular genetics

Genomic DNA (gDNA) from FFPE tumor samples was isolated using the QIAamp DNA Mini kit (Qiagen NV, Venlo, The Netherlands). Search for somatic point mutations in IDH1 Arg132 (exon 4) (GenBank sequence NM_005896) and IDH2 Arg172 (exon 4) (GenBank sequence NM_002168) hot-spot codons was performed by Sanger direct sequencing on an ABI® 3130 Genetic Analyzer (Thermo Fisher Scientific, Inc., Waltham, MA, USA), as published (36). The 1p/19q chromosomal status was assessed by Multiplex Ligation-dependent Probe Amplification (MLPA) using the SALSA-MLPA Kit P088-B2 (MRC-Holland, Amsterdam, The Netherlands), according to the manufacturer's instructions. Fragment analysis was performed on an ABI® 3130 Genetic Analyzer (Thermo Fisher Scientific, Inc.).

GAM frequency and survival analysis

The frequency of GAMs was quantified by counting the number of immunopositive cells for each antibody and for each cell form (see Results) in five randomly selected microscopic high power fields (HPF) at ×400 magnification per section and by calculating the mean values. Only cells were counted the nucleus of which was visible in counterstained sections. The number of GAMs was compared with the three grades (II–IV) of malignancy. CD163 immunohistochemical expression was evaluated according to the average frequency of positive cells (<10, 20–50, 50–100, >100) and distribution (perivascular or scattered in the parenchyma) after examining 5 randomly selected fields per tumor section at ×400 high-power magnification, with a semi-quantitative scoring system including four categories: 0, 1, 2 and 3 (Table II) and compared with the overall survival (OS) of patients. OS was defined as the time from date of diagnosis until the time of death or last follow-up of the patient. The comparison was made also by scoring the CD163 staining in two categories of expression: Low (including the above 0 and 1 categories) and high (including the above 2 and 3 categories) (Table II). The correlation between CD163 expression and OS was investigated in the tumor series also after stratification for IDH1/2 mutation status.

Table II.

Four and two-score system for evaluation of CD163 immunostaining.

Table II.

Four and two-score system for evaluation of CD163 immunostaining.

ScoreFrequency of positive cells (per ×400 HPF)Distribution
0a<10Only perivascular
1a20–50Perivascular and scattered in the parenchyma
2b50–100Perivascular and scattered in the parenchyma
3b>100Perivascular and scattered in the parenchyma

a Low

b high.

Statistical analysis

The correlation between tumor grade and immunohistochemical expression of CD68 or CD163 was analyzed by investigating differences among the groups with a one-way ANOVA and Tukey's post hoc test for multiple comparisons. P<0.05 was considered to indicate a statistically significant difference. Survival curves were estimated using the Kaplan-Meier method and comparison between them were performed by the log-rank test (Mantel-Cox). Data were analyzed with the SPSS v23.0 software (SPSS, Inc., Chicago, IL, USA).


Immunohistochemical analysis

Four groups of GAM forms were identified immunohistochemically, that differed not only for positive or negative staining, but also for staining intensity: i) normal ramified microglia with a small elongated nucleus and polar processes with a radial or longitudinal branching; ii) reactive microglia (RM); iii) cells with a roundish and granular macrophagic form (M); and iv) cells of intermediate form (IF), with very thick and short processes, or simply roundish bumpy cell (BC) forms. The first two cell types stained prevailingly with Iba1 and CD16, the third group with CD68 and CD163 and the last group showed a variable staining with the 4 antibodies.

Normal cortex. Iba1 stained diffusely 10–15 cells per ×400 HPF with thin processes and the typical branching (Fig. 1A). CD68 revealed 7–8 cells per ×400 HPF with a FRP of fine granules in the cytoplasms and/or short processes. CD16 showed the same finding as Iba1. Ischemic neurons showed CD16-positive nuclei with a round or elongated form. CD163 was almost negative.

Gliomas. Gliomas are heterogeneous tumors, therefore, selected areas with defined cell distribution patterns were chosen from all the cases for comparison, corresponding to mild (MIA) and high (HIA) tumor infiltration areas, solid tumor (ST) and regressive areas (RA). In LGG form types 2 and 4 and in HGG types 3 and 4 prevailed. In ST and RA of HGG most part of GAMs were, therefore, positive for CD68 and CD163.

Diffuse astrocytomas. Iba1. In MIA, cells appeared as elegant RM with thin processes, longer than in normal cortex, in number of 20–25 positive cells per ×400 HPF (Fig. 1B). In HIA, they increased progressively with the increase of tumor cell number until to 100–200 cells per ×400 HPF (Fig. 1C). In ST the number of positive cells decreased to 80–120 cells per ×400 HPF and IF and M phenotypes with and without processes prevailed, not only around vessels, but also scattered in the tissue.

CD68. In MIA, RM cells with positive granules in the cytoplasm or short processes occurred in number of 15–20 per ×400 HPF. In HIA, the positive cells increased to 50–100 per ×400 HPF with coarser granules and broader short branching. They assumed the IF or M aspects approaching ST. In the latter, the density of positive cells decreased to 40–50 per ×400 HPF, assuming prevailingly the roundish form of M. Perivascular M clusters could be observed with a frequency depending on the vessel density as well as rare scattered forms. Some IF and most M forms stained more intensely than with Iba1.

CD16. The distribution was similar to that of Iba1 (Fig. 1D). Ischemic neurons entrapped in the tumor appeared as ball-like positive figures.

CD163. Positive cells with a M-like or with an IF or BC appearance were rare and mostly with an intraluminal or perivascular localization; positive cells scattered in ST were even rarer. CD163 was positive only in a quota of CD68+ cells.

Oligodendrogliomas. The tumor growth could be diffuse or nodular. In the first type, GAMs were diffusely increased in number, whereas in the second one GAMs were limited to a thin strip immediately close to the tumor and in ST they were less numerous and mainly IFs or BCs. The findings were similar to those of diffuse astrocytomas, but with a great difference between MIA and HIA: 30–40 vs. > 200 positive cells. In ST (nodular growth), IFs and M forms (Fig. 1E) prevailed on RM phenotype (Fig. 1F), both in perivascular position and scattered in the tissue. CD16 and CD163 behaved as in diffuse astrocytomas. In MIA and HIA most CD163+ cells are perivascular (Fig. 1G). In the same areas, Iba1+ RM did not crowd around small vessels (Fig. 1H).

Anaplastic astrocytomas and oligodendrogliomas. The only difference was that in astrocytomas there was no increase of vessels and, therefore, the number of perivascular M cells did not vary; in anaplastic oligodendrogliomas the vessels increased as well as microvascular proliferations and M forms and IFs increased correspondingly (Fig. 1I). In grade III gliomas an increase of CD163-positive cells was observed (Fig. 1J).

Pilocytic astrocytomas. GAMs showed the same frequency as in diffuse and anaplastic astrocytomas with a prevalence of M forms and IFs.

Glioblastomas. In MIA and HIA the findings were similar to those described in II and III grade gliomas. In ST the number of RM cells strongly reduced and Iba1+/CD16+ IFs and mainly M forms increased (Fig. 2A), especially in perinecrotic or perivascular clusters as CD163+ cells (Fig. 2B). Iba1+ M forms can show a density >200 cells per ×400 HPF, representing >40% of tumor cells (Fig. 2C). In the transition from ST to RA, M-like forms increased. They stained more intensely with CD68 and CD163 (Fig. 2D) than with Iba1 and CD16. In necroses larger than the microscopic field at ×400 HPF, almost all cells could be represented by M forms reaching, therefore, the 100% of cells. IFs stained more intensely with Iba1 and CD16 whereas M forms with CD68 and CD163. GAMs crowded in glomerular structures (Fig. 2E). M cells showed in variable number a nuclear positivity for c-MAF, and this was well evident in c-MAF/CD163 (Fig. 2F) and c-MAF/CD68 double immunostainings.

CD11b and CD45. The former was weakly expressed in a quota of GAMs, whereas the latter was positive in a quota of CD68+ and CD163+ cells. Roughly CD45+ cells corresponded to CD163+ cells (Fig. 2G, H).

In some GBs, CD98 was co-expressed with GFAP in scattered cells in ST areas (Fig. 2I).

Correlation of GAMs with histological grade and with survival

Iba1+ and CD16+ cells prevailed in LGG, whereas CD68+ and CD163+ cells prevailed in HGG. If all GAM forms (RM, BC, IF and M), positive to one of the 4 antibodies were considered, there was no correlation with the histologic grade, because the high number of RM in LGG paralleled that of M forms in HGG. Iba1+ cells did not show a significant difference in number among WHO II–IV grade gliomas, nor CD16+ cells. On the contrary, expression levels of CD68+ and especially CD163+ cells increased with malignancy grade with a statistically significant difference between II and IV grade (Fig. 3). CD163-positive BC and M were definitely in a higher number in HGG than in LGG.

As for survival analysis, considering the whole series of gliomas (WHO grade II–IV), CD163 immunohistochemical expression significantly correlated with a shorter OS for patients, both applying the 4-score system (log-rank test, P=0.0001) and using a 2-score system (log-rank test, P=0.0001) for CD163 (Fig. 4A and B).

Evaluating the correlation between OS and CD163 within each single tumor type and grade, no statistically significant correlation was found. Also considering the group of II grade tumors (astrocytomas and oligodendrogliomas), no correlation emerged, whereas a significant correlation was found in the group of III grade gliomas, astrocytomas + oligodendrogliomas (log-rank test, P=0.028) (Fig. 5A). Considering separately astrocytomas (II and III grade) and oligodendrogliomas (II and III grade), a significant correlation come out (log-rank test, P=0.007 and P=0.008, respectively) (curves not shown). These findings suggested that CD163, evaluated on the whole series of grade II–IV gliomas, has a prognostic value, however, completely absorbed by that of histological grade.

After stratification of patients for IDH1/2 mutation status, no significant correlation between OS and CD163 was found within the LGG series, whereas including III grade tumors a significant correlation was observed, but it reflected that of the histological grade (log-rank test, P=0.001) (Fig. 5B). It is to be remarked that in our series IDH-wild-type II and III grade tumors were very few.

Microglia relationship with the tumor vasculature

In MIA and HIA of LGG, where only in oligodendrogliomas an increase of small vessels occurred in comparison with normal tissue, RM forms tremendously increased, without crowding on single vessels, but showing a high frequency in areas rich in vessels. On the contrary, adherence of single microglia cells to capillaries was frequent. In HGG, GAMs accumulated around vessels either as M forms or IFs and BCs or as unidentifiable forms, because secondary to pathoplastic influences, such as those of cells stretched around vessels.


The greatest information about microglia and GAMs derives from studies on myeloid cells in tissues, in vitro cultures, in animal experimentation and recently from the Two-photon laser scanning microscopy (TPLSM) (3739). The GAM types identified by the four relevant antibodies, more or less correspond to those described in GL-261 glioma model by TPLSM (38). In infiltration areas, there was no doubt on the origin of RM from resident microglia (27), more intensely stained with Iba1 and CD16 than with CD68 and CD163 and almost no macrophage was present (33).

The transition from HIA to ST was marked by an almost disappearance of RM forms, that could be reduced, destroyed or switched to serve a different function. In ST, IFs with thick short processes or BCs and round M forms without processes were found, but in a less number than RM of infiltration areas, with the exception of their clustering around necroses or in perivascular position. They stained more intensely with CD68 and CD163. A quota of M forms were CD45high (11,19,40) and stained with c-MAF (41) and roughly corresponded to CD163+ cells. They correspond, therefore, to blood-borne macrophages, unless resident microglia upregulates CD45 becoming thus responsible for most macrophages in gliomas (27). IFs and BCs can originate either from resident microglia or represent blood-borne macrophages, except that they correspond to the phagocyting cells described by TPLSM (38). In HGG, CD68+ and CD163+ GAMs with M-like morphology prevailed. Contrary to the impression that they represent an immune or cytotoxic defense against the tumor, a pro-tumor function has been attributed to these cells, recruited and stimulated to proliferate by the glioma cells through TGF-β, prostaglandine E2, CCL2, CX3CL1 and colony stimulating factor 1 (CSF-1) (23,26,42). Where the boundary between tumor and normal tissue was sharp, RM cells were limited to a narrow peritumor strip and this supports the idea that migrating neoplastic cells are the main motive of RM proliferation.

In HGG, despite GAMs show complement (CR1, CR3, CR4) and Fc-γ receptors, their phagocytic capacity is considered reduced (23), based on the relief that CR3+ microglia cells were never observed to kill glioma cells (43), but correlated with tumor proliferation rate (44). GAMs don't express cytokines for tumoricidal activity (21); in contrast, glioma-released factors induce in microglia cells, via Toll-like receptors (TLRs), the expression of membrane type 1 matrix metalloprotease (MT1-MMP) that promotes glioma expansion (12,45).

From a neuropathological point of view, one wonders what else CD68+ and CD163+ perinecrotic and perivascular cells could be if not cells phagocyting tumor debris in regressive areas. The same could be true for macrophagic forms scattered in tumor proliferating areas. Here apoptosis occurs correlating with mitoses (46) and its decomposition products are known to be phagocyted in few hours by macrophages (47).

M2 polarized cells are deduced to represent the greatest part of GAMs, independently of their phenotypes, including the rare CD163+ M forms of LGG and the tremendous amount of them in HGG, where it could be secondary to the BBB breakdown. Were it not for the increase of this cell component in GB, it could not be said that GAMs increase in HHG in comparison with LGG, for the great richness of the latter in RM forms. It was observed that M2 GAMs stain by CD163 (4851), or express c-MAF (41), not exclusively, but prevailingly. We confirm this findings, but, at the same time, we remark that the number of CD11b+ cells was too low, so that it could indicate only a quota of cells originating from resident microglia.

The relationship between vessels and GAMs is controversial. They increased near vessels or in infiltration areas in LGG and cluster in perivascular spaces in HGG, but, even if showing direct contacts with capillaries in both tumor types, they did not crowd around the small vessels in infiltration areas. In LGG, the finding of intra- and perivascular GAMs depended on the vessel number, that was higher in oligodendroglioma than in astrocytoma and, together with GAMs scattered in the parenchyma, prevailed in solid tumor upon its periphery. It has been reported that VEGF produced by glioma cells has a chemotactic effect on them, inducing their migration and proliferation in vitro (52) and in vivo (53). GAMs are attracted by vessels and, in turn, promote angiogenesis (54,55). It must be remarked that perivascular IFs and M forms are mainly CD163+.

Despite the literature considers CD16 as indicating M1 (56) and CD163 M2 (31,4850,5759) polarization profile, IFs and BCs, independently of their origin from resident microglia or blood-borne macrophages, are not strictly recognizable as M1 or M2 polarized. It has been rather hypothesized a continuum M1-M2 functional state with the possibility that, upon different stimulations (60), both or neither one is expressed by GAMs (1820,26). It must be considered that microglia cells undergo rapid changes (38), passing cell forms quickly into one another under the influence of the microenvironment; moreover, in compact tumor areas they can be mechanically modified.

The tumorigenetic function of GAMs is supported in vitro by the interaction with glioblastoma stem cells (GSCs), that induce in them an immunosuppressive phenotype (31); GAMs, in turn, enhance the invasiveness of the glioma initiating cells (GICs) (32). In GB, an indirect proof is the correlation of GAMs not only with Ki-67/MIB-1, but also with the stem cell markers Nestin, SOX2 and CD133 (61). Recently, much attention is given to the relationship between GAMs, GSCs and vessels, through CCL2/CCR2, CXCL12/CXCR4, CX3CL1/CX3CR1, CSF-1 and periostin signalings; however, our knowledge on the relations between microglia, tumor cells and other components cannot be considered exhaustive (26).

Finally, in GB, it has been hypothesized a fusion between tumor cells and macrophages, denounced by CD98 positivity (62). This would be in line with the phagocytic capacity maintained in glioma cell lines and fetal rat normal glia (63,64). In our GBs, one wonders whether CD98+ cells are nothing else than macrophages that phagocyted tumor cells, as it happens in non-neoplastic conditions, for example, where GFAP and myelin debris can be found in macrophages.

The inter-grade analysis didn't show a correlation of GAMs with survival if all the microglia forms demonstrated by the four antibodies were considered, because in LGG RM forms can reach the same frequency as M in HGG (4). The correlation with the tumor grade and with survival came out if only CD68+ and CD163+ M forms were considered. In GB, however, CD163+ M forms could not be directly related to malignancy, because they are associated to tumor structures that are typical of the malignant phenotype. The occurrence of CD163+ M forms in perivascular position should mean that they derived from the peripheral blood, because of the BBB disrupture, which already by itself points out malignancy. CD163+ M or IF forms may have different interpretations; it is known that they increase from II to IV tumor grade. Considering together II grade astrocytomas and oligodendrogliomas, no correlation of CD163 expression with OS was found, whereas, in the group of III grade gliomas, a correlation was evident (P=0.028). Also putting together II and III grade astrocytomas or II and III grade oligodendrogliomas, a significant correlation was found. This is quite comprehensible in oligodendrogliomas, where an increase of vessels occurs, but not in astrocytomas, where the number of vessels does not increase. IDH status does not seem to have any correlation with GAMs in II grade gliomas; considering together II and III grade tumors a correlation came out, but also in this case it can be attributed to the short survival of anaplastic oligodendrogliomas.

It must be remarked that the number of CD163+ cells was higher than that of CD45+ cells; this means that M2 polarization could be independent of the origin of microglia.

Today most observations on GAMs demonstrate their favouring function on tumor progression. This conclusion is mainly derived from experiments on animal models and in vitro cultures. In the neuropathological practice, however, uncertainty still exists and the evaluation of GAMs must be given directly on tumor tissue and be part of the prognosis/diagnosis. The answer to the question if GAMs are ‘friends’ or ‘foes’ cannot be so sharp as in experimental condition, also because the increase of CD163+ forms might be secondary and not primary to malignancy.


This study was supported by Cassa di Risparmio di Vercelli Foundation, Vercelli, Italy.





blood-brain barrier


bumpy cell


cluster of differentiation


central nervous system


formalin fixed, paraffin embedded


final reaction products


glioma-associated microglia/macrophages




genomic DNA


glioma initiating cells


haematoxylin and eosin


high grade gliomas


high infiltration area


heat-induced epitope retrieval


high power fields


allograft inflammatory factor 1


isocitrate dehydrogenase


intermediate form




low-grade gliomas


macrophagic form


mild infiltration area




not otherwise specified


regressive area


reactive ramified microglia


solid tumor


Toll-like receptors


two-photon laser scanning microscopy


World Health Organization



Graeber MB and Streit WJ: Microglia: Biology and pathology. Acta Neuropathol. 119:89–105. 2010. View Article : Google Scholar : PubMed/NCBI


Lawson LJ, Perry VH, Dri P and Gordon S: Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain. Neuroscience. 39:151–170. 1990. View Article : Google Scholar : PubMed/NCBI


Kettenmann H, Hanisch UK, Noda M and Verkhratsky A: Physiology of microglia. Physiol Rev. 91:461–553. 2011. View Article : Google Scholar : PubMed/NCBI


Simmons GW, Pong WW, Emnett RJ, White CR, Gianino SM, Rodriguez FJ and Gutmann DH: Neurofibromatosis-1 heterozygosity increases microglia in a spatially-and temporally-restricted pattern relevant to mouse optic glioma formation and growth. J Neuropathol Exp Neurol. 70:51–62. 2011. View Article : Google Scholar : PubMed/NCBI


Klein R and Roggendorf W: Increased microglia proliferation separates pilocytic astrocytomas from diffuse astrocytomas: A double labeling study. Acta Neuropathol. 101:245–248. 2001.PubMed/NCBI


Komohara Y, Ohnishi K, Kuratsu J and Takeya M: Possible involvement of the M2 anti-inflammatory macrophage phenotype in growth of human gliomas. J Pathol. 216:15–24. 2008. View Article : Google Scholar : PubMed/NCBI


Shinonaga M, Chang CC, Suzuki N, Sato M and Kuwabara T: Immunohistological evaluation of macrophage infiltrates in brain tumors. Correlation with peritumoral edema. J Neurosurg. 68:259–265. 1988. View Article : Google Scholar : PubMed/NCBI


Roggendorf W, Strupp S and Paulus W: Distribution and characterization of microglia/macrophages in human brain tumors. Acta Neuropathol. 92:288–293. 1996. View Article : Google Scholar : PubMed/NCBI


Nishie A, Ono M, Shono T, Fukushi J, Otsubo M, Onoue H, Ito Y, Inamura T, Ikezaki K, Fukui M, et al: Macrophage infiltration and heme oxygenase-1 expression correlate with angiogenesis in human gliomas. Clin Cancer Res. 5:1107–1113. 1999.PubMed/NCBI


Badie B and Schartner JM: Flow cytometric characterization of tumor-associated macrophages in experimental gliomas. Neurosurgery. 46:957–962. 2000. View Article : Google Scholar : PubMed/NCBI


Watters JJ, Schartner JM and Badie B: Microglia function in brain tumors. J Neurosci Res. 81:447–455. 2005. View Article : Google Scholar : PubMed/NCBI


Markovic DS, Vinnakota K, Chirasani S, Synowitz M, Raguet H, Stock K, Sliwa M, Lehmann S, Kälin R, van Rooijen N, et al: Gliomas induce and exploit microglial MT1-MMP expression for tumor expansion. Proc Natl Acad Sci USA. 106:pp. 12530–12535. 2009; View Article : Google Scholar : PubMed/NCBI


Zhai H, Heppner FL and Tsirka SE: Microglia/macrophages promote glioma progression. Glia. 59:472–485. 2011. View Article : Google Scholar : PubMed/NCBI


Kaminska B: Microglia in Gliomas: Friend or Foe?Glioma Cell Biology. Sedo A and Mentlein R: Springer-Verlag; Berlin: pp. 241–270. 2014


Schiffer D, Mellai M, Bovio E and Annovazzi L: The neuropathological basis to the functional role of microglia/macrophages in gliomas. Neurol Sci. 2017. View Article : Google Scholar


Gabrusiewicz K, Ellert-Miklaszewska A, Lipko M, Sielska M, Frankowska M and Kaminska B: Characteristics of the alternative phenotype of microglia/macrophages and its modulation in experimental gliomas. PLoS One. 6:e239022011. View Article : Google Scholar : PubMed/NCBI


Durafourt BA, Moore CS, Zammit DA, Johnson TA, Zaguia F, Guiot MC, Bar-Or A and Antel JP: Comparison of polarization properties of human adult microglia and blood-derived macrophages. Glia. 60:717–727. 2012. View Article : Google Scholar : PubMed/NCBI


Perry VH and Teeling J: Microglia and macrophages of the central nervous system: The contribution of microglia priming and systemic inflammation to chronic neurodegeneration. Semin Immunopathol. 35:601–612. 2013. View Article : Google Scholar : PubMed/NCBI


Glass R and Synowitz M: CNS macrophages and peripheral myeloid cells in brain tumours. Acta Neuropathol. 128:347–362. 2014. View Article : Google Scholar : PubMed/NCBI


Szulzewsky F, Pelz A, Feng X, Synowitz M, Markovic D, Langmann T, Holtman IR, Wang X, Eggen BJ, Boddeke HW, et al: Glioma-associated microglia/macrophages display an expression profile different from M1 and M2 polarization and highly express Gpnmb and Spp1. PLoS One. 10:e01166442015. View Article : Google Scholar : PubMed/NCBI


Hussain SF, Yang D, Suki D, Aldape K, Grimm E and Heimberger AB: The role of human glioma-infiltrating microglia/macrophages in mediating antitumor immune responses. Neuro Oncol. 8:261–279. 2006. View Article : Google Scholar : PubMed/NCBI


Parney IF, Waldron JS and Parsa AT: Flow cytometry and in vitro analysis of human glioma-associated macrophages. Laboratory investigation. J Neurosurg. 110:572–582. 2009. View Article : Google Scholar : PubMed/NCBI


Li W and Graeber MB: The molecular profile of microglia under the influence of glioma. Neuro Oncol. 14:958–978. 2012. View Article : Google Scholar : PubMed/NCBI


Wei J, Gabrusiewicz K and Heimberger A: The controversial role of microglia in malignant gliomas. Clin Dev Immunol. 2013:2852462013. View Article : Google Scholar : PubMed/NCBI


Prinz M, Tay TL, Wolf Y and Jung S: Microglia: Unique and common features with other tissue macrophages. Acta Neuropathol. 128:319–331. 2014. View Article : Google Scholar : PubMed/NCBI


Hambardzumyan D, Gutmann DH and Kettenmann H: The role of microglia and macrophages in glioma maintenance and progression. Nat Neurosci. 19:20–27. 2016. View Article : Google Scholar : PubMed/NCBI


Müller A, Brandenburg S, Turkowski K, Müller S and Vajkoczy P: Resident microglia, and not peripheral macrophages, are the main source of brain tumor mononuclear cells. Int J Cancer. 137:278–288. 2015. View Article : Google Scholar : PubMed/NCBI


Zhou W, Ke SQ, Huang Z, Flavahan W, Fang X, Paul J, Wu L, Sloan AE, McLendon RE, Li X, et al: Periostin secreted by glioblastoma stem cells recruits M2 tumour-associated macrophages and promotes malignant growth. Nat Cell Biol. 17:170–182. 2015. View Article : Google Scholar : PubMed/NCBI


Szulzewsky F, Arora S, de Witte L, Ulas T, Markovic D, Schultze JL, Holland EC, Synowitz M, Wolf SA and Kettenmann H: Human glioblastoma-associated microglia/monocytes express a distinct RNA profile compared to human control and murine samples. Glia. 64:1416–1436. 2016. View Article : Google Scholar : PubMed/NCBI


Kennedy BC, Showers CR, Anderson DE, Anderson L, Canoll P, Bruce JN and Anderson RC: Tumor-associated macrophages in glioma: Friend or foe? J Oncol 2013. 4869122013.


Wu A, Wei J, Kong LY, Wang Y, Priebe W, Qiao W, Sawaya R and Heimberger AB: Glioma cancer stem cells induce immunosuppressive macrophages/microglia. Neuro Oncol. 12:1113–1125. 2010. View Article : Google Scholar : PubMed/NCBI


Ye XZ, Xu SL, Xin YH, Yu SC, Ping YF, Chen L, Xiao HL, Wang B, Yi L, Wang QL, et al: Tumor-associated microglia/macrophages enhance the invasion of glioma stem-like cells via TGF-β1 signaling pathway. J Immunol. 189:444–453. 2012. View Article : Google Scholar : PubMed/NCBI


Brandenburg S, Müller A, Turkowski K, Radev YT, Rot S, Schmidt C, Bungert AD, Acker G, Schorr A, Hippe A, et al: Resident microglia rather than peripheral macrophages promote vascularization in brain tumors and are source of alternative pro-angiogenic factors. Acta Neuropathol. 131:365–378. 2016. View Article : Google Scholar : PubMed/NCBI


Coniglio S, Miller I, Symons M and Segall JE: Coculture assays to study macrophage and microglia stimulation of glioblastoma invasion. J Vis Exp. 20:1162016.


Louis DN, Ohgaki H, Wiestler OD and Cavenee WK: WHO classification of tumours of the Central Nervous System. 4th. IARC Press; Lyon: pp. 1–408. 2016


Mellai M, Piazzi A, Caldera V, Monzeglio O, Cassoni P, Valente G and Schiffer D: IDH1 and IDH2 mutations, immunohistochemistry and associations in a series of brain tumors. J Neurooncol. 105:345–357. 2011. View Article : Google Scholar : PubMed/NCBI


Kondo S and Okabe S: In vivo two-photon microscopy of microglia. Methods Mol Biol. 1041:319–335. 2013. View Article : Google Scholar : PubMed/NCBI


Bayerl SH, Niesner R, Cseresnyes Z, Radbruch H, Pohlan J, Brandenburg S, Czabanka MA and Vajkoczy P: Time lapse in vivo microscopy reveals distinct dynamics of microglia-tumor environment interactions-a new role for the tumor perivascular space as highway for trafficking microglia. Glia. 64:1210–1226. 2016. View Article : Google Scholar : PubMed/NCBI


Nimmerjahn A: Two-photon imaging of microglia in the mouse cortex in vivo. Cold Spring Harb Protoc. 5:pii: pdb.prot069294. 2012.


Greter M, Lelios I and Croxford AL: Microglia versus myeloid cell nomenclature during brain inflammation. Front Immunol. 6:2492015. View Article : Google Scholar : PubMed/NCBI


Barros MH, Hauck F, Dreyer JH, Kempkes B and Niedobitek G: Macrophage polarisation: An immunohistochemical approach for identifying M1 and M2 macrophages. PLoS One. 8:e809082013. View Article : Google Scholar : PubMed/NCBI


da Fonseca AC and Badie B: Microglia and macrophages in malignant gliomas: Recent discoveries and implications for promising therapies. Clin Dev Immunol. 2013:2641242013.PubMed/NCBI


Morioka T, Baba T, Black KL and Streit WJ: Immunophenotypic analysis of infiltrating leukocytes and microglia in an experimental rat glioma. Acta Neuropathol. 83:590–597. 1992. View Article : Google Scholar : PubMed/NCBI


Morimura T, Neuchrist C, Kitz K, Budka H, Scheiner O, Kraft D and Lassmann H: Monocyte subpopulations in human gliomas: Expression of Fc and complement receptors and correlation with tumor proliferation. Acta Neuropathol. 80:287–294. 1990. View Article : Google Scholar : PubMed/NCBI


Vinnakota K, Hu F, Ku MC, Georgieva PB, Szulzewsky F, Pohlmann A, Waiczies S, Waiczies H, Niendorf T, Lehnardt S, et al: Toll-like receptor 2 mediates microglia/brain macrophage MT1-MMP expression and glioma expansion. Neuro Oncol. 15:1457–1468. 2013. View Article : Google Scholar : PubMed/NCBI


Schiffer D: Pathology and neuroepidemiology of the brain and nervous system. Curr Opin Oncol. 3:449–458. 1991. View Article : Google Scholar : PubMed/NCBI


Hochreiter-Hufford A and Ravichandran KS: Clearing the dead: Apoptotic cell sensing, recognition, engulfment, and digestion. Cold Spring Harb Perspect Biol. 5:a0087482013. View Article : Google Scholar : PubMed/NCBI


Kamper P, Bendix K, Hamilton-Dutoit S, Honoré B, Nyengaard JR and d'Amore F: Tumor-infiltrating macrophages correlate with adverse prognosis and Epstein-Barr virus status in classical Hodgkin's lymphoma. Haematologica. 96:269–276. 2011. View Article : Google Scholar : PubMed/NCBI


Zaki MA, Wada N, Ikeda J, Shibayama H, Hashimoto K, Yamagami T, Tatsumi Y, Tsukaguchi M, Take H, Tsudo M, et al: Prognostic implication of types of tumor-associated macrophages in Hodgkin lymphoma. Virchows Arch. 459:361–366. 2011. View Article : Google Scholar : PubMed/NCBI


Ino Y, Yamazaki-Itoh R, Shimada K, Iwasaki M, Kosuge T, Kanai Y and Hiraoka N: Immune cell infiltration as an indicator of the immune microenvironment of pancreatic cancer. Br J Cancer. 108:914–923. 2013. View Article : Google Scholar : PubMed/NCBI


Herrera M, Herrera A, Domínguez G, Silva J, García V, García JM, Gómez I, Soldevilla B, Muñoz C, Provencio M, et al: Cancer-associated fibroblast and M2 macrophage markers together predict outcome in colorectal cancer patients. Cancer Sci. 104:437–444. 2013. View Article : Google Scholar : PubMed/NCBI


Forstreuter F, Lucius R and Mentlein R: Vascular endothelial growth factor induces chemotaxis and proliferation of microglial cells. J Neuroimmunol. 132:93–98. 2002. View Article : Google Scholar : PubMed/NCBI


Kerber M, Reiss Y, Wickersheim A, Jugold M, Kiessling F, Heil M, Tchaikovski V, Waltenberger J, Shibuya M, Plate KH and Machein MR: Flt-1 signaling in macrophages promotes glioma growth in vivo. Cancer Res. 68:7342–7351. 2008. View Article : Google Scholar : PubMed/NCBI


Li Y, Liu DX, Li MY, Qin XX, Fang WG, Zhao WD and Chen YH: Ephrin-A3 and ephrin-A4 contribute to microglia-induced angiogenesis in brain endothelial cells. Anat Rec (Hoboken). 297:1908–1918. 2014. View Article : Google Scholar : PubMed/NCBI


Rymo SF, Gerhardt H, Wolfhagen Sand F, Lang R, Uv A and Betsholtz C: A two-way communication between microglial cells and angiogenic sprouts regulates angiogenesis in aortic ring cultures. PLoS One. 6:e158462011. View Article : Google Scholar : PubMed/NCBI


Ding P, Wang W, Wang J, Yang Z and Xue L: Expression of tumor-associated macrophage in progression of human glioma. Cell Biochem Biophys. 70:1625–1631. 2014. View Article : Google Scholar : PubMed/NCBI


Mantovani A, Allavena P and Sica A: Tumour-associated macrophages as a prototypic type II polarised phagocyte population: Role in tumour progression. Eur J Cancer. 40:1660–1667. 2004. View Article : Google Scholar : PubMed/NCBI


Lan C, Huang X, Lin S, Huang H, Cai Q, Wan T, Lu J and Liu J: Expression of M2-polarized macrophages is associated with poor prognosis for advanced epithelial ovarian cancer. Technol Cancer Res Treat. 12:259–267. 2013. View Article : Google Scholar : PubMed/NCBI


Edin S, Wikberg ML, Dahlin AM, Rutegård J, Öberg Å, Oldenborg PA and Palmqvist R: The distribution of macrophages with a M1 or M2 phenotype in relation to prognosis and the molecular characteristics of colorectal cancer. PLoS One. 7:e470452012. View Article : Google Scholar : PubMed/NCBI


Lisi L, Stigliano E, Lauriola L, Navarra P and Dello Russo C: Proinflammatory-activated glioma cells induce a switch in microglial polarization and activation status, from a predominant M2b phenotype to a mixture of M1 and M2a/B polarized cells. ASN Neuro. 6:171–183. 2014. View Article : Google Scholar : PubMed/NCBI


Noorani I, Petty G, Grundy PL, Sharpe G, Willaime-Morawek S, Harris S, Thomas GJ, Nicoll JA and Boche D: Novel association between microglia and stem cells in human gliomas: A contributor to tumour proliferation? J Pathol Clin Res. 1:67–75. 2015. View Article : Google Scholar : PubMed/NCBI


Takeuchi H, Kubota T, Kitai R, Nakagawa T and Hashimoto N: CD98 immunoreactivity in multinucleated giant cells of glioblastomas: An immunohistochemical double labeling study. Neuropathology. 28:127–131. 2008. View Article : Google Scholar : PubMed/NCBI


Huysentruyt LC, Akgoc Z and Seyfried TN: Hypothesis: Are neoplastic macrophages/microglia present in glioblastoma multiforme? ASN Neuro. 3(pii): e000642011.PubMed/NCBI


Bjerknes R, Bjerkvig R and Laerum OD: Phagocytic capacity of normal and malignant rat glial cells in culture. J Natl Cancer Inst. 78:279–288. 1987.PubMed/NCBI

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January 2018
Volume 15 Issue 1

Print ISSN: 1792-1074
Online ISSN:1792-1082

2016 Impact Factor: 1.39
Ranked #68/217 Oncology
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Annovazzi, L., Mellai, M., Bovio, E., Mazzetti, S., Pollo, B., & Schiffer, D. (2018). Microglia immunophenotyping in gliomas. Oncology Letters, 15, 998-1006.
Annovazzi, L., Mellai, M., Bovio, E., Mazzetti, S., Pollo, B., Schiffer, D."Microglia immunophenotyping in gliomas". Oncology Letters 15.1 (2018): 998-1006.
Annovazzi, L., Mellai, M., Bovio, E., Mazzetti, S., Pollo, B., Schiffer, D."Microglia immunophenotyping in gliomas". Oncology Letters 15, no. 1 (2018): 998-1006.