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组氨酸脱羧酶和前列腺素受体的分子生物学。

Molecular biology of histidine decarboxylase and prostaglandin receptors.

机构信息

Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.

出版信息

Proc Jpn Acad Ser B Phys Biol Sci. 2010;86(8):848-66. doi: 10.2183/pjab.86.848.

Abstract

Histamine and prostaglandins (PGs) play a variety of physiological roles as autacoids, which function in the vicinity of their sources and maintain local homeostasis in the body. They stimulate target cells by acting on their specific receptors, which are coupled to trimeric G proteins. For the precise understanding of the physiological roles of histamine and PGs, it is necessary to clarify the molecular mechanisms involved in their synthesis as well as their receptor-mediated responses. We cloned the cDNAs for mouse L-histidine decarboxylase (HDC) and 6 mouse prostanoid receptors (4 PGE(2) receptors, PGF receptor, and PGI receptor). We then characterized the expression patterns and functions of these genes. Furthermore, we established gene-targeted mouse strains for HDC and PG receptors to explore the novel pathophysiological roles of histamine and PGs. We have here summarized our research, which should contribute to progress in the molecular biology of HDC and PG receptors.

摘要

组胺和前列腺素(PGs)作为自体活性物质发挥着多种生理作用,它们在其来源附近发挥作用,维持体内局部的动态平衡。它们通过与三聚体 G 蛋白偶联作用于其特定的受体来刺激靶细胞。为了精确理解组胺和 PGs 的生理作用,有必要阐明它们合成以及受体介导反应中涉及的分子机制。我们克隆了小鼠 L-组氨酸脱羧酶(HDC)和 6 种小鼠前列腺素受体(4 种 PGE(2)受体、PGF 受体和 PGI 受体)的 cDNA。然后,我们对这些基因的表达模式和功能进行了表征。此外,我们还建立了针对 HDC 和 PG 受体的基因靶向小鼠品系,以探索组胺和 PGs 的新的病理生理学作用。我们在这里总结了我们的研究,这应该有助于 HDC 和 PG 受体的分子生物学的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b51e/3037517/31f15333d11f/pjab-86-848-g001.jpg

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