Chen Jiaxuan, Lobachev Kirill S, Grindel Brian J, Farach-Carson Mary C, Hyzy Sharon L, El-Baradie Khairat B, Olivares-Navarrete Rene, Doroudi Maryam, Boyan Barbara D, Schwartz Zvi
Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, USA.
Mol Endocrinol. 2013 Jul;27(7):1065-77. doi: 10.1210/me.2012-1277. Epub 2013 May 9.
Protein disulfide isomerase family A, member 3 (Pdia3) mediates many of the plasma membrane (PM)-associated rapid responses to 1α,25-dihydroxyvitamin D3 (1α,25[OH]2D3). It is not well understood how Pdia3, which is an endoplasmic reticulum (ER) chaperone, functions as a PM receptor for 1α,25(OH)2D3. We mutated 3 amino acids (K214 and R282 in the calreticulin interaction site and C406 in the isomerase catalytic site), which are important for Pdia3's ER chaperone function, and examined their role in responses to 1α,25(OH)2D3. Pdia3 constructs with and without the ER retention signal KDEL were used to investigate the PM requirement for Pdia3. Finally, we determined whether palmitoylation and/or myristoylation were required for Pdia3-mediated responses to 1α,25(OH)2D3. Overexpressing the Pdia3 R282A mutant in MC3T3-E1 cells increased PM phospholipase A2-activating protein, Rous sarcoma oncogene (c-Src), and caveolin-1 but blocked increases in 1α,25(OH)2D3-stimulated protein kinase C (PKC) seen in cells overexpressing wild-type Pdia3 (Pdia3Ovr cells). Cells overexpressing Pdia3 with K214A and C406S mutations had PKC activity comparable to untreated controls, indicating that the native response to 1α,25(OH)2D3 also was blocked. Overexpressing Pdia3[-KDEL] increased PM localization and augmented baseline PKC, but the stimulatory effect of 1α,25(OH)2D3 was comparable to that seen in wild-type cultures. In contrast, 1α,25(OH)2D3 increased prostaglandin E2 in Pdia3[±KDEL] cells. Although neither palmitoylation nor myristoylation was required for PM association of Pdia3, myristoylation was needed for PKC activation. These data indicate that both the chaperone functional domains and the subcellular location of Pdia3 control rapid membrane responses to 1α,25(OH)2D3.
蛋白质二硫键异构酶A家族成员3(Pdia3)介导了许多与质膜(PM)相关的对1α,25 - 二羟基维生素D3(1α,25[OH]2D3)的快速反应。目前尚不清楚作为内质网(ER)伴侣蛋白的Pdia3如何作为1α,25(OH)2D3的质膜受体发挥作用。我们对3个氨基酸(钙网蛋白相互作用位点的K214和R282以及异构酶催化位点的C406)进行了突变,这些氨基酸对Pdia3的内质网伴侣蛋白功能很重要,并研究了它们在对1α,25(OH)2D3反应中的作用。使用带有和不带有内质网滞留信号KDEL的Pdia3构建体来研究Pdia3对质膜的需求。最后,我们确定了Pdia3介导的对1α,25(OH)2D3反应是否需要棕榈酰化和/或肉豆蔻酰化。在MC3T3 - E1细胞中过表达Pdia3 R282A突变体增加了质膜磷脂酶A2激活蛋白、罗氏肉瘤癌基因(c - Src)和小窝蛋白 - 1,但阻断了在过表达野生型Pdia3的细胞(Pdia3Ovr细胞)中观察到的1α,25(OH)2D3刺激的蛋白激酶C(PKC)的增加。过表达带有K214A和C406S突变的Pdia3的细胞具有与未处理对照相当的PKC活性,表明对1α,25(OH)2D3的天然反应也被阻断。过表达Pdia3[-KDEL]增加了质膜定位并增强了基础PKC,但1α,25(OH)2D3的刺激作用与野生型培养物中观察到的相当。相比之下,1α,25(OH)2D3增加了Pdia3[±KDEL]细胞中的前列腺素E2。虽然Pdia3与质膜的结合既不需要棕榈酰化也不需要肉豆蔻酰化,但PKC激活需要肉豆蔻酰化。这些数据表明,Pdia3的伴侣蛋白功能结构域和亚细胞定位都控制着对1α,25(OH)2D3的快速膜反应。