Calcium is critical for controlling the balance of proliferation and differentiation in epidermal keratinocytes. We previously reported that the calcium sensing receptor (CaR) is required for mediating Ca2+ signaling and extracellular Ca2+ (Ca2+o)- induced differentiation. In this study, we investigated the mechanism by which CaR regulates intracellular Ca2+ (Ca2+i) and its role in differentiation. Membrane fractionation, fluorescence immunolocalization, and co-immunoprecipitation studies were performed to assess potential interactions between CaR and other regulators of Ca2+ stores and channels. We found that the glycosylated form of CaR forms a complex with phospholipase C γ1, IP3 receptor (IP3R), and the Golgi Ca2+-ATPase, secretory pathway Ca2+-ATPase 1, in the trans-Golgi. Inactivation of the endogenous CaR gene by adenoviral expression of a CaR antisense cDNA inhibited Ca2+i response to Ca2+o, decreased Ca2+i stores, decreased Ca2+o-induced differentiation, but augmented store-operated channel activity and Ca2+ uptake by intracellular organelles. Our results indicate that CaR regulates keratinocyte differentiation in part by modulating Ca2+i stores via interactions with Ca2+ pumps and channels that regulate those stores. © 2006 The Society for Investigative Dermatology.
CITATION STYLE
Tu, C. L., Chang, W., & Bikle, D. D. (2007). The role of the calcium sensing receptor in regulating intracellular calcium handling in human epidermal keratinocytes. Journal of Investigative Dermatology, 127(5), 1074–1083. https://doi.org/10.1038/sj.jid.5700633
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