Doroudi Maryam, Schwartz Zvi, Boyan Barbara D
School of Biology, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA 23284, USA; Department of Periodontics, University of Texas Health Science Center, San Antonio, TX 78284, USA.
J Steroid Biochem Mol Biol. 2015 Mar;147:81-4. doi: 10.1016/j.jsbmb.2014.11.002. Epub 2014 Nov 6.
The secosteroid 1α,25-dihydroxy vitamin D3 [1α,25(OH)2D3] acts on cells via classical steroid hormone receptor-mediated gene transcription and by initiating rapid membrane-mediated signaling pathways. In its membrane-initiated pathway, after 1α,25(OH)2D3 interacts with protein disulfide isomerase, family A, member 3 (Pdia3) in caveolae, phospholipase A2 (PLA2) and protein kinase C (PKC) are activated. Recent efforts to determine the signaling proteins involved in the 1α,25(OH)2D3 signal from Pdia3 to PLA2 have indicated that phospholipase A2 activating protein (PLAA) and Ca(2+)/calmodulin-dependent kinase II (CaMKII) are required. PLAA is located in caveolae, where it interacts with Pdia3 and caveolin-1 (Cav-1) to initiate rapid signaling via CaMKII, activating PLA2, leading to activation of protein kinase C (PKC) and PKC-dependent responses.
维生素D3的衍生物1α,25 - 二羟基维生素D3 [1α,25(OH)2D3] 通过经典的类固醇激素受体介导的基因转录以及启动快速的膜介导信号通路作用于细胞。在其膜启动途径中,1α,25(OH)2D3与小窝中的蛋白二硫键异构酶A家族成员3(Pdia3)相互作用后,磷脂酶A2(PLA2)和蛋白激酶C(PKC)被激活。最近确定参与从Pdia3到PLA2的1α,25(OH)2D3信号传导的信号蛋白的研究表明,需要磷脂酶A2激活蛋白(PLAA)和钙/钙调蛋白依赖性激酶II(CaMKII)。PLAA位于小窝中,在那里它与Pdia3和小窝蛋白-1(Cav-1)相互作用,通过CaMKII启动快速信号传导,激活PLA2,导致蛋白激酶C(PKC)激活和PKC依赖性反应。