Chondroitin 6-sulfate represses keratinocyte proliferation in mouse skin, which is associated with psoriasis.
Chondroitin 6-sulfate represses keratinocyte proliferation in mouse skin, which is associated with psoriasis.
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硫酸软骨素6抑制小鼠皮肤角质细胞增殖,这与牛皮癣有关。
DOI:
10.1038/s42003-020-01618-5
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发表时间:
2021-01-25
影响因子:
5.9
通讯作者:
Kitagawa H
中科院分区:
文献类型:
--
作者:
Kitazawa K;Nadanaka S;Kadomatsu K;Kitagawa H
Chondroitin sulfates are implicated in epidermal biology, but functional significance of chondroitin sulfates remains unclear. Here, we report that chondroitin 6-sulfate is important for the maintenance of epidermal homeostasis. Mice deficient in chondroitin 6-O-sulfotransferase-1 (C6st-1), which is involved in biosynthesis of chondroitin 6-sulfate, exhibited keratinocyte hyperproliferation and impaired skin permeability barrier function. Chondroitin 6-sulfate directly interacted with the EGF receptor and negatively controlled ligand-induced EGF receptor signaling. Normal function of hyperproliferative C6st-1-knockout mouse-derived keratinocytes was rescued by treatment with exogenous chondroitin 6-sulfate. Epidermal hyperplasia, induced using imiquimod, was more severe in C6st-1-knockout mice than in C6st-1 wild-type mice. Taken together, these findings indicate that chondroitin 6-sulfate represses keratinocyte proliferation in normal skin, and that the expression level of C6st-1 may be associated with susceptibility to psoriasis. Kitazawa et al. show that chondroitin 6-sulfate represses keratinocyte proliferation in skin. They find that mice deficient in chondroitin-6-O-sulfotransferase-1 (C6st-1), which synthesizes chondroitin 6-sulfate, exhibit keratinocyte hyperproliferation and impaired skin permeability barrier. This study suggests that the expression level of C6st-1 may serve as a biomarker for the susceptibility to psoriasis.
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影响因子:
4.8
作者:
Nadanaka, Satomi;Ishida, Miho;Kitagawa, Hiroshi
通讯作者:
Kitagawa, Hiroshi
影响因子:
5.6
作者:
Bocheńska K;Smolińska E;Moskot M;Jakóbkiewicz-Banecka J;Gabig-Cimińska M
通讯作者:
Gabig-Cimińska M
影响因子:
6.8
作者:
Pantazopoulos H;Markota M;Jaquet F;Ghosh D;Wallin A;Santos A;Caterson B;Berretta S
通讯作者:
Berretta S
影响因子:
4.5
作者:
Eames BF;Yan YL;Swartz ME;Levic DS;Knapik EW;Postlethwait JH;Kimmel CB
通讯作者:
Kimmel CB
影响因子:
14
作者:
Hanthamrongwit, M;Reid, WH;Grant, MH
通讯作者:
Grant, MH