跳转至内容
Merck
CN
  • Exogenous R-Spondin1 Induces Precocious Telogen-to-Anagen Transition in Mouse Hair Follicles.

Exogenous R-Spondin1 Induces Precocious Telogen-to-Anagen Transition in Mouse Hair Follicles.

International journal of molecular sciences (2016-04-23)
Na Li, Shu Liu, Hui-Shan Zhang, Zhi-Li Deng, Hua-Shan Zhao, Qian Zhao, Xiao-Hua Lei, Li-Na Ning, Yu-Jing Cao, Hai-Bin Wang, Shuang Liu, En-Kui Duan
摘要

R-spondin proteins are novel Wnt/β-catenin agonists, which signal through their receptors leucine-rich repeat-containing G-protein coupled receptor (LGR) 4/5/6 and substantially enhance Wnt/β-catenin activity. R-spondins are reported to function in embryonic development. They also play important roles in stem cell functions in adult tissues, such as the intestine and mammary glands, which largely rely on Wnt/β-catenin signaling. However, in the skin epithelium and hair follicles, the information about R-spondins is deficient, although the expressions and functions of their receptors, LGR4/5/6, have already been studied in detail. In the present study, highly-enriched expression of the R-spondin family genes (Rspo1/2/3/4) in the hair follicle dermal papilla is revealed. Expression of Rspo1 in the dermal papilla is specifically and prominently upregulated before anagen entry, and exogenous recombinant R-spondin1 protein injection in mid-telogen leads to precocious anagen entry. Moreover, R-spondin1 activates Wnt/β-catenin signaling in cultured bulge stem cells in vitro, changing their fate determination without altering the cell proliferation. Our pioneering study uncovers a role of R-spondin1 in the activation of cultured hair follicle stem cells and the regulation of hair cycle progression, shedding new light on the governance of Wnt/β-catenin signaling in skin biology and providing helpful clues for future treatment of hair follicle disorders.

材料
货号
品牌
产品描述

Sigma-Aldrich
抗活性-β-连环蛋白(抗ABC)抗体,克隆 8E7, clone 8E7, Upstate®, from mouse
Sigma-Aldrich
Anti-Beta Catenin Antibody, clone 7F7.2, clone 7F7.2, Upstate®, from mouse