PDF )   Rev Osteoporos Metab Miner. 2020; 12 (4): 152-154
DOI: 10.4321/S1889-836X2020000400008

Carpintero-Fernández P1, Sánchez Temparno A1, Varela Eírin M1,2, García-Yuste A1, Yáñez Cabanas J3, Díez-Ulloa A3, Caeiro JR3, Mayan MD1
1 CellCOM Research Group. Biomedical Research Institute of A Coruña. A Coruña (Spain)
2 European Research Institute for the Biology of Aging (ERIBA). University Medical Center Groningen (UMCG). University of Groningen (RUG). Groningen (Holland)
3 Department of Orthopedic Surgery and Traumatology. University Hospital Complex of Santiago de Compostela. University of Santiago de Compostela (USC) Santiago de Compostela (Spain)


Osteoarthritis (OA) is one of the most prevalent rheumatic diseases at present. It is characterized by the progressive degeneration of articular cartilage accompanied by alterations in other tissues, such as in the subchondral bone, synovial tissue or muscle. Currently one of the most frequent causes of disability in the aging population worldwide, OA is one of the main causes of chronic pain. From the biomechanical point of view, the joint is involved in maintaining mechanical support by stabilizing movement and flexion. The mechanical consequences of joint degeneration include the loss of stability or increased load stress on the joints, associated with changes in the structure and composition of the articular cartilage. Given that the molecular mechanisms by which joint tissue degradation and the loss of its homeostasis occur are not yet known, the current treatments available are based on the use of anti-inflammatories and pain relief drugs.
Articular cartilage is a tissue with unique mechanical properties formed by a dense extracellular matrix (ECM) that covers the surface of the bone in mobile joints, mainly composed of different types of collagen, proteoglycans and glycoproteins. Chondrocytes, the only cell type described in articular cartilage, are the cells responsible for synthesizing ECM components, as well as maintaining tissue homeostasis. Taking into account the distribution of chondrocytes within cartilage, until a few years ago it was believed that chondrocytes were found in isolation in gaps inserted in the ECM without any type of cellular interaction or communication between them. However, recent results have shown that chondrocytes present cytoplasmic projections that are capable of crossing the ECM and connecting distant cells [1]. In line with these results, it has been shown that chondrocytes express several proteins of the connexin family, involved in cellular communication through gap junctions (GJs). In the case of cartilage, chondrocytes are capable of communicating through connexin channels formed mainly by connexin 43 (Cx43) [2]. Furthermore, through these cytoplasmic projections and gap junctions, chondrocytes are capable of exchanging different metabolites and small molecules such as ATP or RNA in addition to amino acids and proteins [1,3]. On the other hand, several studies indicate that the overactivity of Cx43 triggers an inflammatory and degenerative process related to joint degradation in patients with OA [2]. In our research group we have shown that alterations in Cx43 activity trigger changes in the phenotype of chondrocytes accompanied by an increase in the expression levels of interleukin-1β (IL-1β), cyclooxygenase-2 (COX-2) and metalloprotease-3 (MMP-3) [4] associated with the progress of the disease. The overexpression of Cx43 in a chondrocyte line increases the CD105 and CD166 markers associated with de-differentiated stem cells, as well as the translocation to the nucleus of the Twist-1 transcription factor, which indicates that they could be undergoing a process of epithelium-mesenchyme transition (TEM) [4]. Lastly, Cx43 overactivity is associated with increased levels of senescence markers such as p53, p16 and ß-galactosidase, as well as activation of NF-κβ accompanied by a senescent phenotype and increased secretion of inflammatory cytokines, known as the secretory senescence-associated phenotype (SASP) [4]. These results show that alterations in the expression and activity of Cx43 could be playing an essential role in the development and progression of the disease by modulating the phenotype of the adult chondrocyte. In fact, the decrease in Cx43 activity using different compounds improves the regeneration capacity of different tissues and in different models of age-associated diseases [5,6], reinforcing the role of this transmembrane protein in tissue degeneration and senescence.
More studies are undoubtedly needed in this regard, but with our results, we could conclude that Cx43 is a therapeutic target of interest to maintain the adult chondrocyte phenotype, and avoid processes of de-differentiation and cellular senescence associated with an inflammatory and degenerative phenotype when it is maintained over time (chronically). In fact, in vitro models have already demonstrated its usefulness in reducing cell senescence markers and favoring chondrocyte re-differentiation, restoring tissue regeneration capacity [7-9]. In older adults, it should be noted that recently obtained results by our research group indicate that the increase in Cx43 could also be involved in tissue degeneration and accumulation of senescent cells in cases of intervertebral disc degeneration, suggesting that therapies aimed at modifying Cx43 They could be useful in the treatment of degenerative conditions in the intervertebral disc.
In recent years, different OA modifying drugs have been proposed as new therapeutic strategies because of their ability to promote chondrogenesis, thus promoting re-differentiation of chondrocytes and improving tissue regeneration. On the other hand, molecules capable of reducing Cx43 levels, such as oleuropein [10], improve ECM formation in 3D models by increasing levels of type II collagen and proteoglycans, and also improve the arthritic chondrocyte phenotype by reducing gene expression levels inflammatory interleukins and metalloproteases [10,11].
These and other studies show that high levels of Cx43 in cartilage observed from the first stages of the disease could be related to the activation of degradation processes of articular cartilage by activating the epithelium-mesenchyme transition (cell de-differentiation) and increasing cell senescence synergistically (Figure 1). Undoubtedly, the use of molecules and compounds that decrease the levels or activity of this protein will be of interest for developing new therapeutic strategies for the treatment of degenerative musculoskeletal diseases associated with age, such as osteoarthritis.

Acknowledgments: Our figures have been created using the material available at “Servier Medical Art” (smart.servier.com), and Creative Commons Attribution 3.0. Unported License.

Conflict of interests: The authors declare no conflict of interest.



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