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系统表达分析提示 Plexin-B2 及其配体 Sema4C 参与血管和内分泌系统的调节。

A systematic expression analysis implicates Plexin-B2 and its ligand Sema4C in the regulation of the vascular and endocrine system.

机构信息

Max-Planck-Institute for Heart and Lung Research, Department of Pharmacology, Ludwigstr. 43, 61231 Bad Nauheim, Germany.

出版信息

Exp Cell Res. 2010 Sep 10;316(15):2477-86. doi: 10.1016/j.yexcr.2010.05.007. Epub 2010 May 15.

Abstract

Plexins serve as receptors for semaphorins and play important roles in the developing nervous system. Plexin-B2 controls decisive developmental programs in the neural tube and cerebellum. However, whether Plexin-B2 also regulates biological functions in adult nonneuronal tissues is unknown. Here we show by two methodologically independent approaches that Plexin-B2 is expressed in discrete cell types of several nonneuronal tissues in the adult mouse. In the vasculature, Plexin-B2 is selectively expressed in functionally specialized endothelial cells. In endocrine organs, Plexin-B2 localizes to the pancreatic islets of Langerhans and to both cortex and medulla of the adrenal gland. Plexin-B2 expression is also detected in certain types of immune and epithelial cells. In addition, we report on a systematic comparison of the expression patterns of Plexin-B2 and its ligand Sema4C, which show complementarity or overlap in some but not all tissues. Furthermore, we demonstrate that Plexin-B2 and its family member Plexin-B1 display largely nonredundant expression patterns. This work establishes Plexin-B2 and Sema4C as potential regulators of the vascular and endocrine system and provides an anatomical basis to understand the biological functions of this ligand-receptor pair.

摘要

衔接蛋白作为神经信号分子 semaphorin 的受体,在神经系统发育中发挥重要作用。Plexin-B2 控制着神经管和小脑的决定性发育程序。然而,Plexin-B2 是否也调节成年非神经元组织中的生物学功能尚不清楚。本文通过两种方法独立的方法表明,Plexin-B2 在成年小鼠的几种非神经元组织中的离散细胞类型中表达。在脉管系统中,Plexin-B2 选择性地表达在功能特化的内皮细胞中。在内分泌器官中,Plexin-B2 定位于胰岛和肾上腺的皮质和髓质。Plexin-B2 的表达也在某些类型的免疫细胞和上皮细胞中检测到。此外,本文还报道了 Plexin-B2 与其配体 Sema4C 的表达模式的系统比较,这些配体在某些组织中具有互补性或重叠性,但在其他组织中则没有。此外,本文还证明 Plexin-B2 和其家族成员 Plexin-B1 的表达模式具有很大的非冗余性。这项工作确立了 Plexin-B2 和 Sema4C 作为血管和内分泌系统潜在调节剂的地位,并为理解这一对配体-受体对的生物学功能提供了解剖学基础。

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