Literature DB >> 22515539

Immunohistochemical examination of plexiform-like complex vascular lesions in the lungs of broiler chickens selected for susceptibility to idiopathic pulmonary arterial hypertension.

Krishna R Hamal1, Gisela F Erf, Nicholas B Anthony, Robert F Wideman.   

Abstract

Idiopathic pulmonary arterial hypertension (IPAH) is a disease of unknown cause that is characterized by elevated pulmonary arterial pressure and pulmonary vascular resistance, and by extensive vascular remodelling. In human IPAH patients, remodelling of the pulmonary vasculature results in the formation of plexiform lesions in the terminal pulmonary arterioles. Various molecules are expressed in the human plexiform lesions, including alpha smooth muscle actin, von Willebrand factor, vascular endothelial growth factor, vascular endothelial growth factor receptor type 2, hypoxia inducible factor-1α, survivin, tenascin, collagen, fibronectin, and various immune/inflammatory cells such as, cytotoxic lymphocytes, B lymphocytes, MHC class II cells, and monocytes/macrophages are also present. Plexiform lesions rarely develop in the lungs of laboratory animals, but plexiform-like complex vascular lesions (CVL) do develop spontaneously in the lungs of broiler chickens from an IPAH-susceptible line. To examine angioproliferative and immune-system-related activities associated with CVL in broiler lungs, paraformaldehyde-fixed, paraffin-embedded lung sections from 8-week-old to 24-week-old broiler chickens were stained immunohistochemically using monoclonal or polyclonal antibodies specific for angioproliferative molecules and immune/inflammatory cells. The CVL in the lungs of broiler chickens exhibited positive staining for both angioproliferative molecules and immune/inflammatory cells. These observations combined with the close histological resemblance of broiler CVL to the plexiform lesions of human IPAH patients further validates chickens from our IPAH-susceptible line as an excellent animal model of spontaneous plexogenic arteriopathy.

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Year:  2012        PMID: 22515539     DOI: 10.1080/03079457.2012.663077

Source DB:  PubMed          Journal:  Avian Pathol        ISSN: 0307-9457            Impact factor:   3.378


  7 in total

1.  Involvement of endothelial progenitor cells in the formation of plexiform lesions in broiler chickens: possible role of local immune/inflammatory response.

Authors:  Xun Tan; Fan-Guo Juan; Ali Q Shah
Journal:  J Zhejiang Univ Sci B       Date:  2017 Jan.       Impact factor: 3.066

2.  The growing feather as a dermal test site: Comparison of leukocyte profiles during the response to Mycobacterium butyricum in growing feathers, wattles, and wing webs.

Authors:  G F Erf; I R Ramachandran
Journal:  Poult Sci       Date:  2016-04-14       Impact factor: 3.352

3.  Plexogenic arteriopathy in broiler lungs: Evaluation of line, age, and sex influences.

Authors:  R F Wideman; J G Mason; N B Anthony; D Cross
Journal:  Poult Sci       Date:  2015-02-12       Impact factor: 3.352

4.  Potential contribution of early endothelial progenitor cell (eEPC)-to-macrophage switching in the development of pulmonary plexogenic lesion.

Authors:  Feng-Jin Shao; Xiao-Ling Guo; Jia-Xue Xu; Rui Liu; Dan-Yue Li; Qing-Hao Li; Ting Zhou; Cun Fang; Xun Tan
Journal:  Respir Res       Date:  2022-10-23

5.  Animal Models of Pulmonary Hypertension: Matching Disease Mechanisms to Etiology of the Human Disease.

Authors:  Kelley L Colvin; Michael E Yeager
Journal:  J Pulm Respir Med       Date:  2014-08-04

6.  Transcriptome Analysis and Gene Identification in the Pulmonary Artery of Broilers with Ascites Syndrome.

Authors:  Fei Yang; Huabin Cao; Qingyang Xiao; Xiaoquan Guo; Yu Zhuang; Caiying Zhang; Tiancheng Wang; Huayuan Lin; Yalu Song; Guoliang Hu; Ping Liu
Journal:  PLoS One       Date:  2016-06-08       Impact factor: 3.240

7.  MSC Transplantation Attenuates Inflammation, Prevents Endothelial Damage and Enhances the Angiogenic Potency of Endogenous MSCs in a Model of Pulmonary Arterial Hypertension.

Authors:  Fengjin Shao; Rui Liu; Xun Tan; Qiaoyan Zhang; Lujie Ye; Bingxuan Yan; Ying Zhuang; Jiaxue Xu
Journal:  J Inflamm Res       Date:  2022-03-30
  7 in total

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