Liu Cuiping, Shao Guoli, Lu Yirong, Xue Minmin, Liang Fenfen, Zhang Zhenshu, Bai Lan
Department of Critical Care Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Guang Dong Provincial Key Laboratory of Gastroenterology Department for Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Cell Physiol Biochem. 2018;51(4):1695-1709. doi: 10.1159/000495674. Epub 2018 Nov 30.
BACKGROUND/AIMS: Parathyroid hormone-related protein (PTHrP) is implicated in regulating calcium homeostasis in vertebrates, including sea bream, chick, and mammals. However, the molecular mechanism underlying the function of PTHrP in regulating calcium transport is still not fully investigated. This study aimed to investigate the effect of PTHrP on the calcium uptake and its underlying molecular mechanism in rat enterocytes.
The rat intestinal epithelial cell line (IEC-6) was used. Calcium uptake was determined by using the fluo-4 acetoxymethyl ester fluorescence method. The expression levels of RNAs and proteins was assessed by RT-PCR and Western-blot, respectively.
PTHrP (1-40) induced rapid calcium uptake in enterocytes in a dose-dependent manner. PTHrP (1-40) up-regulated parathyroid hormone 1 receptor (PTHR1) protein but not 1,25D3-MARRS receptor. Pre-treatment of anti- PTHR1 antibody abolished the PTHrP (1-40)-induced calcium uptake. PTHrP (1-40) significantly up-regulated four transcellular calcium transporter proteins, potential vanilloid member 6 (TRPV6), calbindin-D9k (CaBP-D9k), sodium-calcium exchanger 1 (NCX1) and plasma membrane calcium ATPase 1 (PMCA1), in a dose- and time-dependent manner. Pre-treatment with TRPV6 or CaBP-D9k antibodies or knockout of rat TRPV6 or CaBP-D9k markedly inhibited PTHrP (1-40)-induced calcium uptake, whereas inhibition of NCX or PMCA1 by antibodies or inhibitors had no effect on PTHrP(1-40)-induced calcium uptake. Furthermore, PTHrP (1-40) treatment up-regulated protein levels of protein kinase C (PKC α/β) and protein kinase A (PKA). Pretreatment of PKC α/β inhibitor (but not PKA inhibitor) inhibited PTHrP (1-40)-induced calcium uptake.
PTHrP (1-40) stimulates calcium uptake via PTHR1 receptor and PKC α/β signaling pathway in rat enterocytes, and calcium transporters TRPV6 and CaBP-D9k are necessary for this stimulatory effect.
背景/目的:甲状旁腺激素相关蛋白(PTHrP)参与调节脊椎动物(包括海鲷、鸡和哺乳动物)的钙稳态。然而,PTHrP在调节钙转运功能的分子机制仍未得到充分研究。本研究旨在探讨PTHrP对大鼠肠上皮细胞钙摄取的影响及其潜在的分子机制。
使用大鼠肠上皮细胞系(IEC-6)。采用fluo-4乙酰甲酯荧光法测定钙摄取。分别通过逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法评估RNA和蛋白质的表达水平。
PTHrP(1-40)以剂量依赖的方式诱导肠上皮细胞快速摄取钙。PTHrP(1-40)上调甲状旁腺激素1受体(PTHR1)蛋白水平,但未上调1,25-二羟维生素D3膜相关受体(1,25D3-MARRS受体)。抗PTHR1抗体预处理可消除PTHrP(1-40)诱导的钙摄取。PTHrP(1-40)以剂量和时间依赖的方式显著上调四种跨细胞钙转运蛋白,即瞬时受体电位香草酸亚型6(TRPV6)、钙结合蛋白-D9k(CaBP-D9k)、钠钙交换体1(NCX1)和质膜钙ATP酶1(PMCA1)。用TRPV6或CaBP-D9k抗体预处理或敲除大鼠TRPV6或CaBP-D9k可显著抑制PTHrP(1-40)诱导的钙摄取,而抗体或抑制剂对NCX或PMCA1的抑制对PTHrP(1-40)诱导的钙摄取无影响。此外,PTHrP(1-40)处理可上调蛋白激酶C(PKCα/β)和蛋白激酶A(PKA)的蛋白水平。PKCα/β抑制剂(而非PKA抑制剂)预处理可抑制PTHrP(1-40)诱导的钙摄取。
PTHrP(1-40)通过PTHR1受体和PKCα/β信号通路刺激大鼠肠上皮细胞摄取钙,钙转运蛋白TRPV6和CaBP-D9k是这种刺激作用所必需的。