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甲状旁腺激素相关蛋白(PTHrP)在大鼠关节软骨细胞中的作用:PTH(1 - 34)、PTHrP(1 - 34)、PTHrP(1 - 141)、PTHrP(100 - 114) 及针对PTHrP的反义寡核苷酸的比较

Parathyroid hormone-related protein (PTHrP) action in rat articular chondrocytes: comparison of PTH(1-34), PTHrP(1-34), PTHrP(1-141), PTHrP(100-114) and antisense oligonucleotides against PTHrP.

作者信息

Tsukazaki T, Ohtsuru A, Namba H, Oda J, Motomura K, Osaki M, Kiriyama T, Iwasaki K, Yamashita S

机构信息

Department of Cell Physiology, Atomic Disease Institute, Nagasaki University School of Medicine, Japan.

出版信息

J Endocrinol. 1996 Sep;150(3):359-68. doi: 10.1677/joe.0.1500359.

Abstract

Parathyroid hormone-related protein (PTHrP) is thought to be an important autocrine/paracrine factor for chondrocyte metabolism since mice lacking the PTHrP gene exhibit abnormal cartilage development. To determine the biological role of PTHrP in chondrocytes, we first compared the agonist potency of human (h) PTHrP(1-34) with hPTH(1-34) in cultured rat articular chondrocytes. Neither hPTHrP(1-34) nor hPTH(1-34) altered basal DNA synthesis, but attenuated the stimulatory effect of transforming growth factor beta (TGF-beta). Both agents suppressed the expression of alpha(1) type II collagen mRNA in a dose-response fashion with the same potency. In addition, the action of exogenously added hPTHrP(1-34) and hPTH(1-34) on intracellular cAMP and [Ca2+]i levels was similar. We next compared the effect of PTHrP within its entire amino acid sequence (1-141). With regard to thymidine incorporation, alpha(1) type II collagen gene expression and accumulation of cAMP and [Ca2+]i level, there was no significant difference between hPTHrP(1-34) and hPTHrP(1-141). PTHrP C-terminal (100-114) did not show any function. To further investigate PTHrP function, intracellular PTHrP translation was inhibited by a transgene of antisense oligonucleotides against PTHrP. Antisense oligonucleotides decreased PTHrP mRNA translation, specifically inhibited DNA synthesis in control as well as TGF-beta-treated chondrocytes and enhanced alpha(1) type II collagen mRNA expression in TGF-beta-treated chondrocytes. These results suggest that there is no significant difference between exogenously added hPTH(1-34), hPTHrP(1-34) and PTHrP(1-141) with regard to the biological action of these agents, including cell growth, differentiation and second messenger pathway. However, the result of DNA synthesis in the antisense PTHrP-inhibition study suggests that intracellular PTHrP may have an as yet unknown biological role, in addition to a classical PTH/PTHrP receptor-mediated function in the rat articular chondrocyte.

摘要

甲状旁腺激素相关蛋白(PTHrP)被认为是软骨细胞代谢的一种重要自分泌/旁分泌因子,因为缺乏PTHrP基因的小鼠表现出异常的软骨发育。为了确定PTHrP在软骨细胞中的生物学作用,我们首先比较了人(h)PTHrP(1 - 34)与hPTH(1 - 34)在培养的大鼠关节软骨细胞中的激动剂效力。hPTHrP(1 - 34)和hPTH(1 - 34)均未改变基础DNA合成,但减弱了转化生长因子β(TGF - β)的刺激作用。两种药物均以相同效力呈剂量反应方式抑制α1Ⅱ型胶原mRNA的表达。此外,外源性添加的hPTHrP(1 - 34)和hPTH(1 - 34)对细胞内cAMP和[Ca2 + ]i水平的作用相似。接下来,我们比较了PTHrP在其整个氨基酸序列(1 - 141)内的作用。在胸苷掺入、α1Ⅱ型胶原基因表达以及cAMP和[Ca2 + ]i水平的积累方面,hPTHrP(1 - 34)和hPTHrP(1 - 141)之间没有显著差异。PTHrP C末端(100 - 114)未显示任何功能。为了进一步研究PTHrP的功能,通过针对PTHrP的反义寡核苷酸转基因抑制细胞内PTHrP翻译。反义寡核苷酸降低了PTHrP mRNA翻译,特异性抑制了对照以及TGF - β处理的软骨细胞中的DNA合成,并增强了TGF - β处理的软骨细胞中α1Ⅱ型胶原mRNA的表达。这些结果表明,就这些药物的生物学作用而言,包括细胞生长、分化和第二信使途径,外源性添加的hPTH(1 - 34)、hPTHrP(1 - 34)和PTHrP(1 - 141)之间没有显著差异。然而,反义PTHrP抑制研究中的DNA合成结果表明,除了在大鼠关节软骨细胞中经典PTH/PTHrP受体介导的功能外,细胞内PTHrP可能还有一个未知的生物学作用。

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