Literature DB >> 7621779

Myoendothelial junctional complexes in postobstructive pulmonary vasculopathy: a quantitative electron microscopic study.

R P Michel1, F Hu, B O Meyrick.   

Abstract

Postobstructive pulmonary vasculopathy (POPV), produced by chronic unilateral ligation of one pulmonary artery, is characterized by (1) marked proliferation of bronchial collateral vessels, (2) increased pulmonary vascular resistance, and (3) hyperreactivity of arteries to serotonin and of veins to histamine. Electron microscopic examination of the vessels in POPV suggested an increase in myoendothelial junctional complexes (MEJC). To quantitate this change, the number of MEJC in the vessel walls of the left lung was compared with that of the right lung in 16 dogs after ligation of the left main pulmonary artery for 8.4 +/- 1.6 (SE) months. The lungs were fixed by airway instillation of 3% glutaraldehyde. Electron micrographs were taken of pulmonary arteries, capillaries, and veins and of bronchial vessels, and their external diameter and length of endothelial basal lamina were measured. The MEJC were counted and expressed as number per length of basal lamina and typed: Type I consisted of endothelial processes, type II of smooth muscle or pericyte processes, and type III of processes from each cell type. The results demonstrated that the vasculature from the control lung had the smallest number of MEJC and the majority were type I. With ligation, there was a significant increase (p < .01) in the number of MEJC for each type of vessel examined, but no significant change in the distribution of the type. In addition, no correlation was found between the number of MEJC and vascular diameter. It can be concluded that MEJC are increased in each region of the lung's vasculature in POPV and that they may play a role in the proliferative response of the bronchial vasculature, the remodeling of the pulmonary vasculature, and the pulmonary vascular hyperreactivity of this model.

Entities:  

Mesh:

Year:  1995        PMID: 7621779     DOI: 10.3109/01902149509023718

Source DB:  PubMed          Journal:  Exp Lung Res        ISSN: 0190-2148            Impact factor:   2.459


  7 in total

Review 1.  Structure and composition of pulmonary arteries, capillaries, and veins.

Authors:  Mary I Townsley
Journal:  Compr Physiol       Date:  2012-01       Impact factor: 9.090

2.  Exercise physiological responses to drug treatments in chronic thromboembolic pulmonary hypertension.

Authors:  Athanasios Charalampopoulos; J Simon R Gibbs; Rachel J Davies; Wendy Gin-Sing; Kevin Murphy; Karen K Sheares; Joanna Pepke-Zaba; David P Jenkins; Luke S Howard
Journal:  J Appl Physiol (1985)       Date:  2016-07-14

Review 3.  Endothelial and Smooth Muscle Cell Interactions in the Pathobiology of Pulmonary Hypertension.

Authors:  Yuansheng Gao; Tianji Chen; J Usha Raj
Journal:  Am J Respir Cell Mol Biol       Date:  2016-04       Impact factor: 6.914

4.  Localized expression of an Ins(1,4,5)P3 receptor at the myoendothelial junction selectively regulates heterocellular Ca2+ communication.

Authors:  Brant E Isakson
Journal:  J Cell Sci       Date:  2008-11-01       Impact factor: 5.285

Review 5.  The myoendothelial junction: breaking through the matrix?

Authors:  Katherine R Heberlein; Adam C Straub; Brant E Isakson
Journal:  Microcirculation       Date:  2009-03-26       Impact factor: 2.628

Review 6.  Polarized Proteins in Endothelium and Their Contribution to Function.

Authors:  Abigail G Wolpe; Claire A Ruddiman; Phillip J Hall; Brant E Isakson
Journal:  J Vasc Res       Date:  2021-01-27       Impact factor: 1.934

7.  Mitochondrial transplantation attenuates hypoxic pulmonary hypertension.

Authors:  Liping Zhu; Jiwei Zhang; Juan Zhou; Yankai Lu; Songling Huang; Rui Xiao; Xiangyuan Yu; Xianqin Zeng; Bingxun Liu; Fangbo Liu; Mengxiang Sun; Mao Dai; Qiang Hao; Jiansha Li; Tao Wang; Tongfei Li; Qinghua Hu
Journal:  Oncotarget       Date:  2016-08-02
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.