Introduction
The mammalian alveolar epithelium is composed of type I alveolar epithelial cells (AECI) and type II alveolar epithelial cells (AECII). AECI are broad and flat cells that cover 95% of the alveolar surface and comprise 40% of the alveolar epithelium, which is important for gas exchange. AECII are cuboidal cells characterized by the distinct morphological appearance of lamellar bodies, which occupy only 5% of the alveolar surface and comprise 60% of the alveolar epithelium. AECII synthesize, secrete and recycle lung surfactant, which includes surfactant protein (SP)A, SPB, SPC and SPD, reducing surface tension and preventing the collapse of the alveolus (1). AECII also provide pulmonary host defense by synthesizing and secreting numerous cytokines and interleukins that affect lymphocyte, macrophage, and neutrophil functions. Moreover, AECII act as progenitor cells for AECI in the alveoli, and play a key role in maintaining normal alveolar homeostasis and lung repair (2). The inadequate, delayed, or impaired re-epithelialization of the injured alveolus is known as a key factor in the pathogenesis of several life-threatening pulmonary diseases, such as chronic obstructive pulmonary disease (COPD) (3) and acute respiratory distress syndrome (ARDS) (4). A variety of methods for isolating human AECII have been published and some of their properties have been described (5–7); however, it still remains unclear as to how to maintain the proliferation and phenotype of the AECII. A number of difficulties still exist in obtaining an adequate tissue supply to isolate human AECII. Human embryonic stem cells (ESCs) are pluripotent stem cells derived from embryos at the blastocyst stage. ESCs can proliferate indefinitely while maintaining their capacity to differentiate into a great variety of specialized cell types (8,9). ESCs have been induced to differentiate into AECII in vitro and in vivo (10,11). Furthermore, the transplantation of human ESC-derived AECII has been shown to abrogate acute lung injury in mice (12). Thus, AECII derived from exogenous stem cells may provide novel treatment options for COPD.
However, the acquirement of human ESCs implies the destruction of human embryo, which results in obvious ethical debates (13). Human amniotic fluid stem cells (AFSCs) can be isolated from discarded amniocentesis specimens or post-partum amniotic fluid, which is not subject to teratocarcinoma formation and serious ethical issues (14,15). AFSCs possess not only high proliferation potential in vitro, but also a wide range of differentiation potential into cell types from all 3 embryonic germ layers, such as adipocytes, chondrocytes, osteocytes, hepatocytes, neural cells and cardiomyocytes (16–18). Hence, AFSCs are considered new pluripotent stem cells between ESCs and adult stem cells. Their characteristics, including pluripotency, high proliferation rates, multi-differentiation capabilities and lack of ethical issues associated with the retrieval of these cells render them an attractive source for cell therapy, drug discovery and toxicology screening (14–18). Certain studies have demonstrated that human AFSCs can integrate into the murine lung and differentiate into pulmonary lineages following lung injury in vivo (19). However, it remains unknown as to whether amniotic fluid-derived mesenchymal stem cells (AFMSCs) can be induced to differentiate into AECII in vitro. Thus, in the present study, we investigated the potential of AFMSC differentiation into AECII in vitro using KnockOut™ serum replacement (KOSR), activin A and small airway basal medium (SABM).
Materials and methods
Isolation and culture of AFMSCs
Fifteen independent samples of amniotic fluid (20 ml each) were obtained from pregnant women at 16–20 weeks of pregnancy who underwent amniocentesis for fetal karyotyping. The samples were filtered through a 200 mesh filter and centrifuged for 5 min at 1,200 rpm. The cells derived from the amniotic fluid were resuspended in low glucose Dulbecco’s modified Eagle’s medium (DMEM; Gibco, Carlsbad, CA, USA) containing 5 mg/l basic fibroblast growth factor (bFGF; Sigma, St. Louis, MO, USA) and 10% fetal bovine serum (FBS; HyClone, Logan, UT, USA), and maintained in 6-well plates. When the cells were incubated for 3 days at 37°C in a humidified atmosphere of 5% carbon dioxide and 95% air, the supernatants were removed and the cell clones in spindle-shaped growth were selected to other wells by cell scrapers. When the cells reached 80–90% confluence, they were digested using 0.25% trypsin (Sigma) and incubated in a 25 cm2 cell culture flask (Corning Inc.-Life Sciences, Oneonta, NY, USA), labeled as P1 (the first generation). The surface antigens of the AFMSCs (P4) were detected by flow cytometry with monoclonal antibodies as follows: phycoerythrin (PE)-conjugated antibodies against CD29, CD73, CD105 and CD166, and fluorescein isothiocyanate (FITC)-conjugated antibodies against CD14, CD19, CD34, CD44, CD45 and CD90 (BD Biosciences, San Diego, CA, USA). The related isotype control was used as a negative control. The results were analyzed using a flow cytometer (Guava EasyCyte; Millipore, Billerica, MA, USA). Octamer-binding transcription factor 4 (OCT4) mRNA expression in the AFMSCs was detected by reverse transcription-polymerase chain reaction (RT-PCR). The primers were designed as follows (Invitrogen, Shanghai, China): OCT4 (GenBank: DQ486513.1), 5′-CGTG AAGCTGGAGAAGGAGAAGCTG-3′ (sense) and 5′-CAAGGG CCGCAGCTTACACATGTTC-3′ (antisense); and beta-actin (ACTB), 5′-GGCACCACACCTTCTACAATGA-3′ (sense) and 5′-TCAGGAGGAGCAGCAATGATCTTG-3′ (antisense). The protein expression of OCT4 was detected by western blot analysis. Human embryonic stem cells (hES3; ES Cell International, Melbourne, Australia) were used as positive controls and human lung fibroblasts (HFL1; ATCC, Manassas, VA, USA) were used as negative controls. The protocol was approved by the Ethics Committee of Zhejiang Provincial People’s Hospital and each patient signed written informed consent.
Differentiation of AFMSCs in vitro
The AFMSCs (P4) were detached and dissociated into single cells with a mixture of 0.25% trypsin (Sigma)/0.02% EDTA-Na2 in phosphate-buffered saline (PBS). The AFMSCs were seeded into 24-well low-adherence tissue culture plates (Corning Inc.-Life Sciences) at the concentration of 2×107/l/well. They were then divided into 4 groups, named groups I–IV. The AFMSCs were induced to differentiate in vitro using KOSR (Invitrogen, Carlsbad, CA, USA), activin A (PeproTech, Rocky Hill, NJ, USA) and SABM (Lonza, Basel, Switzerland) by different methods. In group I, the AFMSCs were cultured for 3 days suspended in DMEM (Gibco) containing 10% KOSR firstly, and then transferred onto adherent agarose-coated plates. The adherent cells were cultured for 4 days in DMEM containing 10% KOSR with 100 mg/l activin A in a humidified atmosphere of 5% carbon dioxide and 95% air at 37°C. The cells were then cultured for 10 days in DMEM containing 15% KOSR. In group II, the AFMSCs were cultured for 3 days suspended in DMEM containing 10% KOSR firstly, and then adherently cultured for 4 days in DMEM containing 10% KOSR. The cells were then cultured for 10 days in DMEM containing 15% KOSR. In group III, the AFMSCs were cultured for 3 days suspended in DMEM containing 10% KOSR with 100 mg/l activin A firstly, and then cultured for 4 days adherently in DMEM containing 10% KOSR. The cells were then cultured for 10 days in DMEM containing 15% KOSR. In group IV, the AFMSCs were cultured for 3 days suspended in DMEM containing 10% KOSR with 100 mg/l activin A firstly, and then adherently cultured for 4 days in DMEM containing 10% KOSR with 100 mg/l activin A. The cells were then cultured for 10 days in DMEM containing 15% KOSR. Finally, all the cells were cultured for 14 days in SABM.
Quantitative reverse transcription PCR
Total RNA was extracted from the cells using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the instructions of the manufacturer and dissolved in nuclease-free water. The final RNA concentrations were determined using a spectrophotometer. Total RNA was reverse transcribed using MMLV reverse transcriptase (Promega, Madison, WI, USA) at 42°C for 60 min and 70°C for 10 min. Real-time PCR analysis was carried out using SYBR-Green Real-Time PCR Master Mix (Toyobo, Osaka, Japan) and real-time PCR amplification equipment. The thermal profile consisted of one cycle at 95°C for 15 min, followed by 45 cycles at 95°C for 15 sec and 60°C for 30 sec. The primers used were as follows (Invitrogen, Shanghai, China): SPA forward, 5′-CCTATCATTTGCCAA GAACC-3′ and reverse, 5′-CAGGAAGATGGGTTTGGAT-3′; SPC forward, 5′-CAACGGGAAAGGAAACGC-3′ and reverse, 5′-GCTGCTTTATTCTGTTGTGGC-3′; and ACTB forward, 5′-CTACAATGAGCTGCGTGTGGC-3′ and reverse, 5′-CAGG TCCAGACGCAGGATGGC-3′. The mRNA expression of SPA and SPC was determined by normalization of the threshold (Ct) cycle of the target genes to that of the mRNA expression of ACTB for each sample. The ΔCt value was determined using the following equation: (ΔCt) = (Ct of the target genes) - (Ct of ACTB). The ΔΔCt value was used to find the relative expression of the target genes according to the following formula: relative expression 0= 2−ΔΔCt. Data were analyzed using the 2−ΔΔCt method. A549 lung epithelial cells (Shanghai Institute of Biology, Chinese Academy of Sciences, Shanghai, China) were used as the positive controls. Undifferentiated AFMSCs were used as the negative controls.
Western blot analysis
The cells were lysed in ice-cold lysis buffer [50 mmol/l Tris (pH 7.5), 150 mmol/l NaCl, 1 mmol/l EDTA, 10 mmol/l Na2P2O7, 100 mmol/l NaF and 1% Triton X-100] and protease inhibitor cocktail (1 mmol/l phenylmethylsulfonyl fluoride, 1 mg/l aprotinin and 1 mg/l leupeptin). The protein concentration was measured using a protein assay kit (Micro BCA; Pierce, Rockford, IL, USA). Equal amounts of cell lysates containing 10 μg protein were incubated for 5 min in boiling water. Proteins were separated by 8% sodium dodecyl sulfate polyacrylamide gel electrophoresis and then electroblotted onto Hybond-ECL nitrocellulose membranes. The membranes were blocked with TBS solution containing 5% skim milk at room temperature for 1 h. The membranes were then incubated with primary antibodies for 1 h at room temperature on an orbital shaker. The membranes were then washed 5 times, for 5 min each, in Tris-buffered saline with Tween-20 (TBST) and incubated in diluted peroxidase-conjugated immunopure goat anti-rabbit IgG (H+L) (Pierce) for 1 h at room temperature on an orbital shaker. After the membranes were again washed 5 times for 5 min each in TBST, the proteins were visualized with an enhanced chemiluminescence solution (Amersham Pharmacia Biotech, Buckinghamshire, UK). The images were developed on X-ray film and the band densities were analyzed with a UVP-GDS8000 gel analysis system. The same membranes were stripped and blotted with anti-β-actin antibodies, which provided a loading control. The primary antibodies were obtained from the following sources: OCT4 antibody, SPA antibody and SPC antibody from Abcam (Cambridge, MA, USA), and β-actin (N-21) antibody from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA). Protein markers were obtained from Cell Signaling Technology (Danvers, MA, USA).
Immunofluorescence
The differentiated AFMSCs were fixed for 20 min at 4°C with 4% paraformaldehyde (Merck, Darmstadt, Germany). The cells were blocked for 20 min at 37°C with 5% goat serum (diluted in TBS and 0.25% Triton X-100; Sigma), followed by incubation for 2 h at 37°C with a polyclonal rabbit anti-human SPA and SPC antibody (1:500; BD Biosciences). The cells were then rinsed twice for 5 min with PBS, and further incubated for 1 h at 37°C with the secondary antibody FITC-conjugated goat anti rabbit IgG (1:250; BD Biosciences). Each antibody was diluted in PBS with 0.25% Triton X-100. The cell nuclei were then counterstained with 1 g/l 4′,6-diamino-2-phenylindole (DAPI; Sigma) in PBS for 5 min and covered with Immu-Mount (Thermo Electron Corp., Waltham, MA, USA). Finally, all the slides were analyzed using an IX71 fluorescence microscope (Olympus, Tokyo, Japan).
Electron microscopy
The cells were fixed for 1 h in 2.5% glutaraldehyde and 0.1 mmol/l cacodylate buffer, pH 7.4. After a brief rinse in 0.2 mmol/l buffer, the cells were postfixed for 2 h in 1% osmium tetroxide in 0.1 mmol/l cacodylate buffer, pH 7.4. The cells were dehydrated in 90, 95 and 100% hydroxypropyl methacrylate and embedded in Epon-Araldite. Ultrathin serial sections (100 nm) were obtained by an ultramicrotome (RMC, Tucson, AZ, USA) equipped with a diamond knife. The sections were stained with uranyl acetate and lead citrate, and then observed under a transmission electron microscope (Hitachi, Tokyo, Japan).
Statistical analysis
Data were analyzed for statistical significance by one-way analysis of variance (ANOVA), paired-sample t-tests, and multiple comparisons in ANOVA were analyzed using the Student-Newman-Keuls test. Data are expressed as the means ± standard deviation (SD). Values of P<0.05 were considered to indicate statistically significant differences.
Results
Phenotypic characterization of AFMSCs
The surface antigenic characteristics of the AFMSCs were analyzed using flow cytometry. The results revealed that the expression of surface antigens, such as CD29 (73.7±6.6%), CD44 (49.7±4.7%), CD73 (53.0±3.6%), CD90 (54.4±4.35%), CD105 (22.5±2.7%) and CD166 (22.7±3.6%) was positive; however, the expression of CD14 (0.25±0.02%), CD19 (0%), CD34 (0%) and CD45 (0%) was negative (Fig. 1). OCT4, at both the mRNA and protein level was significantly expressed in the AFMSCs (P<0.05) (Fig. 2).
mRNA expression of SPA and SPC in differentiated AFMSCs
The mRNA expression of SPA and SPC in the A549 lung epithelial cells (positive controls) was strongly positive. The mRNA expression of SPA and SPC was not detected in the undifferentiated AFMSCs. When the AFMSCs were induced to differentiate using KOSR only, the mRNA expression of SPA and SPC was negative (group II). When the AFMSCs were induced to differentiate using a combination of KOSR, activin A and SABM, the mRNA expression of SPA and SPC (group III and IV) was still almost undetectable. The mRNA expression of SPA and SPC in the cells in group I was significantly induced, and was the highest amongst all the groups (P<0.05) (Fig. 3).
Protein expression of SPA and SPC in differentiated AFMSCs
When the AFMSCs were induced to differentiate for 31 days, the protein expression of SPA and SPC was detected by western blot analysis and immunofluorescence. The results revealed that the expression of SPA and SPC in group I was significantly induced (P<0.05), but was negative in the cells in the other groups (Fig. 4), which indicates that the AFMSCs can be induced to differentiate into AECII-like cells under specific conditions.
Ultrastructural evidence of AFMSCs differentiating into AECII-like cells
When the AFMSCs were induced to differentiate for 31 days using KOSR, activin A and SABM, lamellar bodies that contained pulmonary surfactant proteins and lipids were observed in the differentiated AFMSCs in group I under a transmission electron microscope (Fig. 5). However, lamellar bodies were not observed in the cells in groups II–IV. This indicates that AFMSCs can differentiate into AECII-like cells by using the appropriate induction medium with KOSR, activin A and SABM.
Discussion
AFMSCs are pluripotent stem cells, which can be isolated from discarded amniocentesis specimens or post-partum amniotic fluid (14,20). Previous studies have demonstrated that AFMSCs express mesenchymal stem cell markers, such as CD90, CD105, CD73 and CD166, but not do not express the hematopoietic markers, CD45, CD34 and CD14 (20–22). In the present study, AFMSCs significantly expressed surface antigens, such as CD29, CD44, CD73 and CD90, but did not express CD14, CD19, CD34 and CD45, which was consistent with the study of Tsai et al (14). The potency of amniotic fluid-derived stem cells in differentiating into cell types from all 3 embryonic germ layers, including endothelial cells, chondrocytes, adipocytes, hepatocytes, neuronal cells and myocytes seems to be between ESCs and adult stem cells (16–18,23). The POU transcription factor, OCT4, is a specific marker for embryonal carcinoma cells, embryonic germ cells and embryonic stem cells (24). In the present study, OCT4 was significantly expressed in the AFMSCs, which indicated that the AFMSCs have pluripotent characteristics. Thus, their pluripotency, lack of ethical issues associated with their acquirement and the lack of teratoma formation when injected in vivo render them attractive candidates for stem cell sources in the field of lung regeneration (14–18).
As progenitors of AECI, AECII characterized by the unique ability to synthesize and secrete SPC and the distinct morphological appearance of lamellar bodies play important roles in lung tissue repair (1). Severe damage to or the loss of AECII may result in a considerable vulnerability of the alveolus and the impairment of alveolar repair (25–27). AECII derived from exogenous stem cells are a promising source of cells which may be used therapeutically to treat distal lung diseases, including COPD. However, to date, there are still no reports on the differentiation of AFMSCs into AECII in vitro (16,28). Small airway growth medium (SAGM) composed of SABM and a commercial cocktail of growth factors is a medium designed for the maintenance and growth of mature distal airway epithelial cells. However, certain studies have shown that SABM significantly improves distal lung epithelial differentiation from mouse ESCs compared with SAGM (29). Thus, in the present study, SABM was used to induce AFMSC differentiation in vitro in place of SAGM. KOSR is a defined medium supplement designed to directly replace FBS in ESC culture medium. Certain studies have shown that definitive endoderm differentiation is improved (30) and human ESCs are induced to differentiate into AECII by the replacement of FBS with KOSR (11). In the present study, AFMSCs failed to differentiate into AECII when induced with only KOSR. Activin A belongs to the transforming growth factor-β (TGF-β) family of growth and differentiation factors (31). Studies on amphibians and have mice shown that high activity of activin signaling is necessary to specify the endoderm germ layer (32,33). It has also been demonstrated that activin A can increase the expression of early distal lung epithelial markers, enhance endoderm formation and accelerate early lung epithelial differentiation (29). In the present study, when the AFMSCs were induced to differentiate for 31 days by KOSR, activin A and SABM, the mRNA and protein expression of SPA and SPC was strongly positive in the differentiated AFMSCs in group I, and lamellar bodies were also observed in the differentiated AFMSCs. However, negative results were observed for the other cell groups, which suggests that the differentiation of AFMSCs is precisely controlled by both time and space. In conclusion, AFMSCs can be induced to differentiate into AECII-like cells in vitro using a combination of KOSR, activin A and SABM under the appropriate conditions, which indicates that AFMSCs have the potential for use in lung regenerative therapy. However, the exact mechanisms of AFMSC differentiation into AECII reamin unknown, and thus, further studies are required in the near future.