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磷酸肌醇的药理学,多种细胞功能的调节因子

Pharmacology of phosphoinositides, regulators of multiple cellular functions.

作者信息

Balla T

机构信息

Endocrinology and Reproduction Research Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Curr Pharm Des. 2001 Apr;7(6):475-507. doi: 10.2174/1381612013397906.

Abstract

Inositol phospholipids represent a small fraction of the phospholipids present in all cellular membranes with remarkable importance in regulating various cell functions. They are synthesized from phosphatidylinositol by sequential phosphorylations on the several hydroxyls of the inositol ring to create polyphosphoinositides that function either as docking sites to promote formation of molecular signaling complexes, or serve as precursors for soluble inositol polyphosphates that act as diffusible intracellular messengers. Phosphoinositides are involved in the control of many processes, including membrane traffic, endo- and exocytosis, mitogenesis and apoptosis. Pharmacological tools have helped to clarify many details of phosphoinositide metabolism and have unveiled the roles of these lipids in the control of specific signaling pathways. However, because of their pleiotropic functions it has been questionable whether pharmacological manipulation of inositide formation and metabolism can be of therapeutic value. This review briefly summarizes the means by which inositide functions have been pharmacologically manipulated, and discusses possibilities for specifically targeting certain aspects of their regulatory functions.

摘要

肌醇磷脂在所有细胞膜的磷脂中占比很小,但在调节各种细胞功能方面具有重要意义。它们由磷脂酰肌醇通过肌醇环上几个羟基的顺序磷酸化合成,生成多磷酸肌醇,这些多磷酸肌醇既可以作为促进分子信号复合物形成的对接位点,也可以作为可溶性肌醇多磷酸的前体,后者作为可扩散的细胞内信使发挥作用。磷酸肌醇参与许多过程的控制,包括膜运输、胞吞和胞吐、有丝分裂和细胞凋亡。药理学工具有助于阐明磷酸肌醇代谢的许多细节,并揭示了这些脂质在控制特定信号通路中的作用。然而,由于它们具有多效性功能,肌醇形成和代谢的药理学操作是否具有治疗价值一直存在疑问。本综述简要总结了药理学上操纵肌醇功能的方法,并讨论了特异性靶向其调节功能某些方面的可能性。

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