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1,25-二羟基维生素D3通过提高磷脂酶C水平上调人角质形成细胞中的磷脂酰肌醇信号通路。

1,25-Dihydroxyvitamin D3 upregulates the phosphatidylinositol signaling pathway in human keratinocytes by increasing phospholipase C levels.

作者信息

Pillai S, Bikle D D, Su M J, Ratnam A, Abe J

机构信息

Department of Medicine, University of California, San Francisco, USA.

出版信息

J Clin Invest. 1995 Jul;96(1):602-9. doi: 10.1172/JCI118075.

Abstract

1,25-Dihydroxyvitamin D3 (1,25(OH)2D3) induces the differentiation of normal human keratinocytes, in part by increasing their basal intracellular calcium levels (Cai) over a period of hours. Agonists such as ATP acting through membrane receptors cause an immediate but transient increase in Cai accompanied by an increase in inositol trisphosphate (IP3). Treatment of keratinocytes for 24 h with 1 nM 1,25(OH)2D3 resulted in a two- to four-fold potentiation of the Cai response of these cells to ATP. This potentiation was inhibitable with cycloheximide, unaccompanied by a change in total intracellular calcium pools, but associated with an increase in basal IP3 levels and ATP-stimulated IP3 production. Treatment with 1,25(OH)2D3 raised the protein and mRNA levels of phospholipase C isoenzymes, particularly phospholipase C-beta 1 in a dose-dependent manner. These studies indicate that 1,25(OH)2D3 modulates the keratinocyte signal transduction pathway by induction of phospholipase isoenzymes, a previously undescribed action for this hormone.

摘要

1,25 - 二羟基维生素D3(1,25(OH)2D3)可诱导正常人角质形成细胞分化,部分原因是在数小时内提高其基础细胞内钙水平(Cai)。通过膜受体起作用的激动剂(如ATP)会导致Cai立即但短暂升高,并伴有肌醇三磷酸(IP3)增加。用1 nM 1,25(OH)2D3处理角质形成细胞24小时,会使这些细胞对ATP的Cai反应增强两到四倍。这种增强作用可被放线菌酮抑制,且细胞内总钙库无变化,但与基础IP3水平升高及ATP刺激的IP3产生增加有关。用1,25(OH)2D3处理会以剂量依赖方式提高磷脂酶C同工酶的蛋白质和mRNA水平,尤其是磷脂酶C - β1。这些研究表明,1,25(OH)2D3通过诱导磷脂酶同工酶来调节角质形成细胞信号转导途径,这是该激素以前未被描述的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d44/185235/99ec27cd0203/jcinvest00013-0621-a.jpg

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