The Role of Connexins and Pannexins in the Cell Communications of Bone Cells

LIU Wen-jing, ZHANG De-mao, ZHOU Xue-dong, XIE Jing

Abstract

Connexins and Pannexins play important roles in osteocytes and osteoblasts differentiation, intracellular signal transduction, maintenance of bone balance, and bone regeneration. This article reviews the progress and limitations of Connexins-mediated gap junctions and Pannexins mediated hemichannel in bone. Current research has shown that these molecules, in the form of gap junctions or separate hemichannels, deliver external stimuli to the skeletal system. However, little is known about the role of other cell types in bone development and homeostasis, such as pre-osteoblasts and bone marrow mesenchymal stem cells, in maintaining normality. In addition, at present, the most well-studied member of the Connexins family is Connexin43 (Cx43), while the roles and mechanisms of other members in bone development are still behind the veil. Gene-edited animal models provide basic information on the role of Connexins and Pannexins in the skeletal system, but the similarities and differences between Connexins and Pannexins remain to be discovered. Targeting a specific function of Connexins or Pannexins for bone stimulation and bone disease remains a challenge, with pharmacological selective overlap between channels, compensation of other subtypes, differences in methods for assessing channel function, and genetic changes associated with transgenic mouse models. Therefore, better tools and research pathways are needed to understand the role of these pathways in bone and cartilage. An essential task for future research will be to identify specific compounds that regulate Connexins or Pannexins subtypes to enable them to be used as pharmaceutical agents in the treatment of bone diseases, providing the possibility to develop new therapeutic strategies for improving bone health and treating diseases of the skeletal system.

 

Keywords: Connexins, Pannexins, Osteocyte, Osteoblast, Cell communication

 

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References


PLOTKIN L I, STAINS J P. Connexins and pannexins in the skeleton: gap junctions, hemichannels and more. Cell Mol Life Sci,2015,72(15): 2853–2867.

DONAHUE H J, QU R W, GENETOS D C. Joint diseases: from connexins to gap junctions. Nat Rev Rheumatol,2018,14(1): 42–51.

PLOTKIN L I, DAVIS H M, CISTERNA B A, et al. Connexins and pannexins in bone and skeletal muscle. Curr Osteoporos Rep,2017,15(4): 326–334.

BRÜCHER B L, JAMALL I S. Cell-cell communication in the tumor microenvironment, carcinogenesis, and anticancer treatment. Cell Physiol Biochem,2014,34(2): 213–243.

KUMAR V, COUSER N L, PANDYA A. Oculodentodigital dysplasia: a case report and major review of the eye and ocular adnexa features of 295 reported cases. Case Rep Ophthalmol Med, 2020, 4: 6535974[2020-05-25]. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7165356/. doi: 10.1155/2020/6535974.

ROY S, JIANG J X, LI A F, et al. Connexin channel and its role in diabetic retinopathy. Prog Retin Eye Res,2017,61: 35–59.

BEYER E C, BERTHOUD V M. Gap junction gene and protein families: connexins, innexins, and pannexins. Biochim Biophys Acta Biomembr, 2018,1860(1): 5–8.

RODRÍGUEZ-SINOVAS A, RUIZ-MEANA M, DENUC A, et al. Mitochondrial Cx43, an important component of cardiac preconditioning. Biochim Biophys Acta Biomembr,2018,1860(1): 174–181.

TOTLAND M Z, RASMUSSEN N L, KNUDSEN L M, et al. Regulation of gap junction intercellular communication by connexin ubiquitination: physiological and pathophysiological implications. Cell Mol Life Sci, 2020,77(4): 573–591.

EPIFANTSEVA I, SHAW R M. Intracellular trafficking pathways of Cx43 gap junction channels. Biochim Biophys Acta Biomembr,2018, 1860(1): 40–47.

HERVE J C, DERANGEON M. Gap-junction-mediated cell-to-cell communication. Cell Tissue Res,2013,352(1): 21–31.

WILLEBRORDS J, MAES M, CRESPO YANGUAS S, et al. Inhibitors of Connexin and Pannexin channels as potential therapeutics. Pharmacol Ther,2017,180: 144–160.

SCEMES E, VELÍŠKOVÁ J. Exciting and not so exciting roles of Pannexins. Neurosci Lett,2019,695: 25–31.

CARPINTERO-FERNANDEZ P, GAGO-FUENTES R, WANG H Z, et al. Intercellular communication via gap junction channels between chondrocytes and bone cells. Biochim Biophysica Acta Biomembr,2018, 1860(12): 2499–2505.

LIU W, ZHANG D, LI X, et al. TGF-β1 facilitates cell-cell communication in osteocytes via Connexin43- and Pannexin1-dependent gap junctions. Cell Death Discov, 2019, 5: 141[2020-05-25]. https://www. nature.com/articles/s41420-019-0221-3. doi: 10.1038/s41420-019-0221-3. PLOTKIN L I, LAIRD D W, AMEDEE J. Role of Connexins and Pannexins during ontogeny, regeneration, and pathologies of bone. BMC Cell Biol, 2016, 17 (Suppl 1): 19[2020-05-25]. https://bmcmolcellbiol. biomedcentral.com/articles/10.1186/s12860-016-0088-6. doi: 10. 1186/s12860-016-0088-6.

STAINS J P, CIVITELLI R. Connexins in the skeleton. Semin Cell Dev Biol,2016,50: 31–39.

PACHECO-COSTA R, DAVIS H M, SORENSON C, et al. Defective cancellous bone structure and abnormal response to PTH in cortical bone of mice lacking Cx43 cytoplasmic C-terminus domain. Bone,2015,81: 632–643.

LIN F X, ZHENG G Z, CHANG B, et al. Connexin 43 modulates osteogenic differentiation of bone marrow stromal cells through gsk-3beta/beta-catenin signaling pathways. Cell Physiol Biochem,2018,47(1): 161–175.

BUO A M, TOMLINSON R E, EIDELMAN E R, et al. Connexin43 and Runx2 interact to affect cortical bone geometry, skeletal development, and osteoblast and osteoclast function. J Bone Miner Res,2017,32(8): 1727–1738.


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