Each Cx has four hydrophobic transmembranes (M1-M4), two extracellular areas (E1 and E2) that bind to another Cx in the neighboring cell, and three cytoplasmic regions that correspond to the cytoplasmic loop (CL), and the amino-terminal (NT), and carboxy-terminal (CT) tail regions. The N-terminus, membrane-spanning sections, and extracellular loops are consistent throughout the structure; however, the size and structure of the CL and the CT are not. The GJ channel is composed of two hemichannels (or connexons), consisting of six transmembrane proteins (Cx subunits) connected to the plasma membrane of each symmetric cell. When two hemichannels join to produce a cell-cell conduit, one is tilted by 30° with respect to the other. Homotypic GJs are formed when identical Cx subunits dock, whereas heterotypic GJs are formed when two different connexons (hemichannels) dock (10). The central cytoplasmic part and the second extracellular domain (E2) regulate the heterotypic adaptation of Cxs. Heterotypic channels have features that differ from those of homotypic channels, such as unitary conductance and gating. The permeabilities of different channels formed by different Cxs differ, allowing secondary messengers to be discriminated against (cyclic guanosine monophosphate, Ca²⁺, or IP₃) (Fig. 1).

Hemichannels regulate cellular responses to a wide range of physiological, oxidative, and metabolic stressors, whereas GJs permit intercellular trans- mission (Fig. 1). Molecules transported through these channels are responsible for several physiological functions. Different stimuli, including variations in voltage, Ca2⁺, pH, and Cx phosphorylation, can dynamically control gap junctional intercellular communication (GJIC) (10-15). Voltage sensitivity is critical for controlling the intercellular connectivity of excitable cells. Channel independence has been demonstrated in the context of cellular proliferation, attachment, motility, apoptotic processes, and signaling (2,12,16-19). It was also recently revealed by the authors' research group that Cx43 levels regulate angiogenesis in endothelial cells (ECs), irrespective of GJ function (2). Moorby and Patel conducted extensive research on the GJ-dependent and-independent functions of Cx43 and discovered that the carboxyl region of Cx43 mainly governs the independent GJ function (19). It is increasingly accepted that the effects of GJIC-independent Cxs on carcinogenesis extend beyond proliferation and migration, including angiogenesis and cell death (20-23).

Angiogenesis plays a crucial role in tissue growth, wound healing (WH), carcinogenesis, and metastasis (1,24). It begins with the growth and development of preexisting vessels, depending on a mixture of growth factors and proangiogenic cytokines, and is regulated by various neovascularization antagonists (Fig. 2) (25,26). Cxs have been shown to affect angiogenic processes in various ways, including growth, transport, and cellular stiffness (27). The roles of Cx43, Cx37, and Cx40, which are the most prevalent Cxs engaged in angiogenic processes, are discussed in the next section. The expression of Cx43 expression influences the angiogenic potential of endothelial cells independently of the GJ interaction. Because proliferation was unchanged, it was hypothesized that the Cx43 protein may significantly alter endothelial cell relocation, thereby promoting angiogenesis (2).

Decreased Cx43 expression can result in vascular dysfunction and impaired angiogenesis (28). Cx43 is also involved in regulating lung microvascular permeability, and its modulation is related to endothelial monolayer permeability (29,30). Salmina et al examined GJ-dependent neurogenesis and concluded that alterations in Cx43 expression were correlated with distinct steps in neural growth (31). Cx43 is also upregulated in ECs during hemodynamic stimulation-induced angiogenesis (32). A study of the molecular processes during human trophoblast fusion revealed that protein kinase A-dependent phosphorylation of Cx43 enhances cell fusion (33). Furthermore, decreased Cx43 expression can result in improper embryo implantation and inadequate angiogenesis (34). It has also been found that Cx43, as a negative regulator, participates in critical steps of WH, such as inflammation response, remodeling of the extracellular matrix, proliferation of epidermal/skin cells, and migration (35).

Cx37 and Cx40, which are co-expressed in ECs, have overlapping functions. Cx40 can promote EC migration, vessel sprouting, and expansion, whereas Cx40 deficiency and inhibition reduce angiogenesis (36). Endothelial Cx40, according to Haefliger et al, affects the initial phases of angiogenesis in the retina by controlling vascularization (37). In Cx37^−/− mice, improved recovery of the hind limb was associated with increased vasculogenesis, which resulted in greater collateral remodeling and angiogenesis (38). Furthermore, the global deletion of Cx37 in mice causes increased angiogenesis during tissue injury, aiding the recovery process after ischemic injury (39). Growth inhibition mediated by Cx37 involves CT and the pore-forming domain (14). Nitric oxide affects endothelial vasomotor activity by modulating calcium signaling (40). Cx37 and Cx40 have been shown to uniquely control post-ischemic limb perfusion, affecting the intensity of ischemic stress and, as a result, post-ischemic persistence (41). Cx37 selectively affects Ang II signaling by modulating Ang II receptor expression (42). Cx37 also suppresses the proliferation of vascular and cancer cells. Cx37-induced growth arrest or growth-permissive phenotypes depend on conformational changes in Cx37 caused by phosphorylation (43).

Different layers of the human epidermis express different levels of Cxs, which are associated with a number of skin diseases (Fig. 3). During the early phases of WH, Cx43 has been observed to be negatively regulated at the wound margins (46). Nitric oxide, a mediator of vasomotion, has been reported to be a strong modulator of GJ coupling in ECs (47). It promotes the de novo formation of GJ by expanding the integration of Cx40 into the plasma membrane. One of the most evident applications that demonstrates the involvement of Cxs in angiogenesis is the efficacy of bioactive glass (BG) in WH. In rats, BG stimulates GJIC, which results in increased angiogenesis and accelerates the closure of excisional wounds (48). It was recently shown that BG affects the expression of Cx43 and ROS levels, increasing WH by suppressing pyroptosis through the Cx43/ROS signaling pathway (49). Cx43 remodeling is an important event in WH that influences the cellular dynamics of keratinocytes and fibroblasts (50). It was revealed that siRNA knockdown of Cx43 in human microvascular endothelial cells reduced migration in vitro, as measured by a wound assay, and impaired aortic vessel sprouting ex vivo (16); Cx43 and the tyrosine phosphatase, SHP-2, were also revealed to mediate endothelial cell migration, revealing a novel interaction between Cx43 and SHP-2 that is required for this process (16).

Mutations in Cx26, Cx30, and Cx31 are associated with hyperproliferative skin diseases (51). Furthermore, suppression of Cx43 function affects the expression of genes associated with WH (52). Cx mutations are associated with epidermal dysplasia (15). Gain-of-function mutations alter Cx-mediated calcium signaling within the epidermis; for example, suppressing Cx43 activity in fibroblasts has been shown to increase migration and control the expression of genes associated with WH through the mitogen-activated protein kinase, specificity protein 1, activator protein 1, glycogen synthase kinase 3, and transforming growth factor pathways, contributing to rapid and scarless WH in the human gingiva (52).

Preclinical studies on peptide therapeutics, a mimetic of Cx43 CT, have reported improvements in WH (53). Cx43 has also been reported to counter-regulate caveolin-1 in controlling EC proliferation and migration, and this counterregulatory effect of Cx43 could be used in therapeutic angiogenesis (54). Morphine administration was found to inhibit angiogenesis and delay WH by upregulating Cx43, and high doses of morphine alter Cx43 expression by increasing fibronectin and actin levels through the activation of transforming growth factor signaling (55). A Cx43 mimetic peptide (TAT-Gap19) significantly upregulates matrix metalloproteinases, tenascin-C, and vascular endothelial growth factor (VEGF)-A (13).

In cancer cells, intercellular communication is aberrant, and numerous studies have suggested that dysfunctional GJ and Cxs play a key role in this process (56). However, there appears to be a skewed association between Cxs and cancer, with evidence suggesting that Cxs may limit cancer cell development in certain instances while also promoting cancer cell motility, invasion, and metastatic dissemination in others (57,58). A key study revealed that inhibiting Cx37 decreases tumor angiogenesis; moreover, Cx37 and Cx40 work together to promote tumorigenesis (20). Consequently, the involvement of Cxs and GJs in cancer is more complex than previously thought.

Breast tumor cells transplanted into heterozygous Cx43 mice did not affect tumor growth, but greatly improved vascularization, indicating the role of Cx43 in vessel quiescence control and pathological tumor angiogenesis (22). The passage of tumor cells through the endothelial barrier is an important step in metastasis, in which endothelial cells adhere to the target organ by direct cell-cell communication and paracrine activation to initiate angiogenesis (Fig. 4). Cx46 regulates cancer stem cell and epithelial-to-mesenchymal transition features in breast cancer cells, suggesting that it may be useful in the development of future cancer therapeutics (59).

Intercellular communication is also required for tumor cell trafficking across the lymphatic endothelium (60). Hemichannels have been reported to facilitate interactions between cancer cells and blood vessels, leading to angiogenesis. Choudhary et al revealed that tumors downregulate Cx43 function, allowing the endothelium to respond to angiogenic stimuli, leading to pathogenic angiogenesis (22). The roles of Cx and Notch endothelial signaling in coordinating the appropriate proliferation and angiogenesis of ECs have been identified (61). It has also been shown that GJIC inhibits tumor growth by transferring microRNAs from one EC to surrounding tumor cells, indicating a bystander role that can be exploited in cancer treatment (21).

Targeting Cx may be a promising therapeutic approach for cancer (23). Exosomes containing anti-angiogenic microRNAs released immediately through Cx channels can prevent cancer cells from promoting angiogenesis (21). Peptide-mediated inhibition of Cx40 in EC is a successful anti-angiogenesis approach that suppresses tumor angiogenesis (36). In the conditioned medium, tumor size and vessel density in Cx43-knockdown tumor cells decreased, indicating that Cx43 prevented tumor growth by decreasing angiogenesis (62).

Several Cxs are co-expressed in the heart; in particular, distinct combinations of Cx40, Cx43, and Cx45 are observed in functionally specialized cardiomyocytes (Fig. 5). GJ channels in the cardiovascular system regulate vascular tone, which is essential for the coordination of cell activity, by permitting the transport of chemical messengers and energy substrates (63-65). Cxs form GJs for the transmission of precisely choreographed current flow patterns that control the synchronized beat of a healthy heart. Several pathophysiological conditions, including atherosclerosis, hypertension, hypertrophy, ischemia, and arrhythmias, have been linked to dysregulation of Cxs in the cardiovascular system in terms of expression, function, posttranslational modifications, and location. Ugwu et al reported a recurring somatic Cx43-gene c.121G>T mutation as a cause of cutaneous venous abnormalities (66). Although Cx43 levels are high in cardiac neural crest cells, both heterozygous and homozygous knock-in mice live long and do not exhibit symptoms of coronary heart disease (67). Similarly, point mutations in Cx43 were not found to cause the tetralogy of Fallot (68).

Treatment with granulocyte colony-stimulating factor improves arterial and capillary density and increases Cx43 expression in failing hearts (69). Through Cx43, VEGF stimulates endothelial progenitor cells and supports vascular healing (70). In ECs, ischemia/reperfusion causes reactive species to disrupt Cx/pannexin signaling mitochondrial prompt division and promote macrovesicle release (71). Cx43 and angiogenesis levels are higher in the exercised mouse heart, indicating increased remodeling (72). Long-term alienation combined with moderate environmental pressure has been associated with depressive symptoms and aberrant expression of Cx43 and Cx45 in the left ventricle (73). Notably, EC-specific molecule 1 enhances the potential of induced pluripotent stem ECs to promote angiogenesis and neovascularization (74). Su et al determined that preconditioning for ischemia had cardioprotective effects on arrhythmia and myocardial recovery by upregulating phosphatidylinositol 3-kinase-mediated Cx43 signaling (75). In a study on myometrial cell patch transplantation to cure myocardial infarction, angiogenesis was reported to occur in the trans- planted myometrium and Cx43 expression was observed in the transplanted patches (76). Cx43 passivation from intercellular signaling and buildup at the mitochondrial inner membrane has been revealed in diabetic cardiomyocytes, demonstrating that mtCx43 is responsible for triggering aberrant contraction and disrupting electrophysiology in cardiomyocytes (77).

Heart disease caused by myocardial tissue injury and fibrosis is related to Cx43-based GJs. As a result, several Cx43 mimetic peptides have been proposed as potential therapeutics for Cx43-related degenerative disorders, some even reaching human clinical trials (78). Cx43 improves infarcted heart angiogenesis, as evidenced by higher levels of VEGF and basic fibroblast growth factor (18). The cardioprotective properties of expanded umbilical cord mesenchymal stem cells (MSC) were attributed to paracrine substances that tend to enhance angiogenesis and preserve Cx43 GJ function (75). Cx43 was found to be dispensable for the adipogenic differentiation of early-stage MSC, although it was protective against cell senescence (79). The survival and tube formation of MSCs are improved by Ang II treatment and Cx43 expression (80). TEM immunogold studies on rat heart ventricles indicated the lack of Cx26 at intercalated discs but the presence of Cx26 at various subcellular compartments (17). It was found that after a localized ischemic stroke, Cx43 regulated the angiogenesis of Buyang Huanwu decoction through VEGF and Ang-1 (81). Due to the increase of tissue Cx43 and proangiogenic markers, regenerative treatment using nanofiber-expanded hematopoietic stem cells has been reported to have a favorable effect on rat heart function following myocardial infarction (82).