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血管生成素-2在淋巴管发育中的免疫组织化学证明

Immunohistochemical demonstration of Angiopoietin-2 in lymphatic vascular development.

作者信息

Shimoda Hiroshi

机构信息

Department of Human Anatomy, Faculty of Medicine, Oita University, 1-1 Idaigaoka, Hasama-machi, Yufu, Oita, 879-5593, Japan.

出版信息

Histochem Cell Biol. 2009 Feb;131(2):231-8. doi: 10.1007/s00418-008-0513-9. Epub 2008 Oct 3.

DOI:10.1007/s00418-008-0513-9
PMID:18836739
Abstract

The cellular expression of Angiopoietin-2 (Ang2) was studied during lymphatic development in mouse by immunohistochemistry and compared to that of lymphatic endothelial markers. At the earliest stage of lymphvasculogenesis, Prox1-identified lymphatic precursor cells of the cardinal vein displayed an intense immunoreaction for Ang2 in their cytoplasm, implying that Ang2 may adjust lymphatic specification and sprouting from the veins under the control of Prox1. Thereafter, Ang2 was constantly expressed in Prox1 and/or LYVE-1-immunopositive endothelial cells of lymphatic sacs and vessels, ranging from lymphatic capillaries to collectors, throughout embryonic and neonatal development, and the lymphatic endothelial cells simultaneously exhibited immunoreactivity to Tie2, a primary receptor for angiopoietins. These results suggest that lymphatic endothelial cells may regulate lymphatic development via their own Ang2-Tie2 signaling. Ang2 is further immunolocalized in the developing blood vessels including hepatic sinusoids, adrenal medullary vasculature and postnatal pulmonary vessels, thereby indicating that the blood vessels, which undergo vascular remodeling and sudden alteration of blood flow during the development, are also likely to express Ang2. The present study is first to demonstrate Ang2 expression in the lymphatic endothelial cells during development, and consequently Ang2 is regarded as a molecular profile of the developing lymphatic endothelial cells required for lymphatic vascular organization.

摘要

通过免疫组织化学方法研究了血管生成素-2(Ang2)在小鼠淋巴管发育过程中的细胞表达,并与淋巴管内皮标志物的表达进行了比较。在淋巴管生成的最早阶段,Prox1识别的主静脉淋巴管前体细胞在其细胞质中对Ang2表现出强烈的免疫反应,这意味着Ang2可能在Prox1的控制下调节淋巴管的特化和从静脉的出芽。此后,在整个胚胎和新生儿发育过程中,Ang2在淋巴管和血管的Prox1和/或LYVE-1免疫阳性内皮细胞中持续表达,范围从淋巴毛细管到收集器,并且淋巴管内皮细胞同时对血管生成素的主要受体Tie2表现出免疫反应性。这些结果表明,淋巴管内皮细胞可能通过其自身的Ang2-Tie2信号传导调节淋巴管发育。Ang2进一步免疫定位在发育中的血管中,包括肝血窦、肾上腺髓质脉管系统和出生后肺血管,从而表明在发育过程中经历血管重塑和血流突然改变的血管也可能表达Ang2。本研究首次证明了Ang2在发育过程中淋巴管内皮细胞中的表达,因此Ang2被视为淋巴管组织发育所需的发育中淋巴管内皮细胞的分子特征。

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