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胰腺β细胞信号转导的新方面。

Novel aspects on pancreatic beta-cell signal-transduction.

机构信息

The Rolf Luft Research Center for Diabetes and Endocrinology L1:03, Karolinska Institutet, SE-17176 Stockholm, Sweden.

出版信息

Biochem Biophys Res Commun. 2010 May 21;396(1):111-5. doi: 10.1016/j.bbrc.2010.02.174.

Abstract

Pancreatic beta-cells release insulin in appropriate amounts in order to keep blood glucose levels within physiological limits. Failure to do so leads to the most common metabolic disorder in man, diabetes mellitus. The glucose-stimulus/insulin-secretion coupling represents a sophisticated interplay between glucose and a variety of modulatory factors. These factors are provided by the blood supply (such as nutrients, vitamins, incretins etc.), the nerval innervations, cell-cell contacts as well as by paracrine and autocrine feedback loops within the pancreatic islet of Langerhans. However, the underlying mechanisms of their action remain poorly understood. In the present mini-review we discuss novel aspects of selective insulin signaling in the beta-cell and novel insights into the role of higher inositol phosphates in insulin secretion. Finally we present a newly developed experimental platform that allows non-invasive and longitudinal in vivo imaging of pancreatic islet/beta-cell biology at single-cell resolution.

摘要

胰腺β细胞以适当的量释放胰岛素,以将血糖水平保持在生理范围内。如果不能做到这一点,就会导致人类最常见的代谢紊乱,即糖尿病。葡萄糖刺激/胰岛素分泌偶联代表了葡萄糖与多种调节因子之间的复杂相互作用。这些因素由血液供应(如营养物质、维生素、肠促胰岛素等)、神经支配、细胞间接触以及胰岛内的旁分泌和自分泌反馈环提供。然而,它们作用的潜在机制仍知之甚少。在本综述中,我们讨论了β细胞中选择性胰岛素信号传递的新方面,以及更高的肌醇磷酸在胰岛素分泌中的作用的新见解。最后,我们介绍了一种新开发的实验平台,该平台允许以单细胞分辨率进行非侵入性和纵向活体成像胰岛/β细胞生物学。

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