Literature DB >> 2007619

Heterogeneity of microvascular pericytes for smooth muscle type alpha-actin.

V Nehls1, D Drenckhahn.   

Abstract

Microvascular pericytes are believed to be involved in various functions such as regulation of capillary blood flow and endothelial proliferation. Since pericytes represent a morphologically heterogeneous cell population ranging from circular smooth musclelike to elongated fibroblast-like morphology it is possible that regulation of blood flow (via contractility) and control of endothelial proliferation (as well as other metabolic functions) may be accomplished by different subsets of pericytes. In the present study we provide evidence for heterogeneity of pericytes at the molecular level by using two novel technical approaches. These are (a) immunostaining of whole mounts of the microvascular beds of the rat mesentery and bovine retina and (b) immunoblotting studies of microdissected retinal microvessels. We show that pericytes of true capillaries (midcapillaries) apparently lack the smooth muscle isoform of alpha-actin whereas transitional pericytes of pre- and postcapillary microvascular segments do express this isoform. Thus, regulation of capillary blood flow may be accomplished by the smooth muscle-related pre- and postcapillary pericytes whereas the nonmuscle pericytes of true capillaries may play a role in other functions.

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Year:  1991        PMID: 2007619      PMCID: PMC2288926          DOI: 10.1083/jcb.113.1.147

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  22 in total

1.  Retinal vascular patterns. VI. Mural cells of the retinal capillaries.

Authors:  T KUWABARA; D G COGAN
Journal:  Arch Ophthalmol       Date:  1963-04

2.  Simultaneous localization of multiple tissue antigens using the peroxidase-labeled antibody method: a study on pituitary glands of the rat.

Authors:  P K Nakane
Journal:  J Histochem Cytochem       Date:  1968-09       Impact factor: 2.479

3.  Differences in pericyte contractile function in rat cardiac and skeletal muscle microvasculatures.

Authors:  R G Tilton; C Kilo; J R Williamson; D W Murch
Journal:  Microvasc Res       Date:  1979-11       Impact factor: 3.514

4.  Actin expression in smooth muscle cells of rat aortic intimal thickening, human atheromatous plaque, and cultured rat aortic media.

Authors:  G Gabbiani; O Kocher; W S Bloom; J Vandekerckhove; K Weber
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5.  An activated form of transforming growth factor beta is produced by cocultures of endothelial cells and pericytes.

Authors:  A Antonelli-Orlidge; K B Saunders; S R Smith; P A D'Amore
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

6.  Pericytes, like vascular smooth muscle cells, are immunocytochemically positive for cyclic GMP-dependent protein kinase.

Authors:  N C Joyce; P DeCamilli; J Boyles
Journal:  Microvasc Res       Date:  1984-09       Impact factor: 3.514

7.  Heterogeneity of myosin antigenic expression in vascular smooth muscle in vivo.

Authors:  D M Larson; K Fujiwara; R W Alexander; M A Gimbrone
Journal:  Lab Invest       Date:  1984-04       Impact factor: 5.662

Review 8.  Pulmonary hypertension. Anatomic and physiologic correlates.

Authors:  B Meyrick; L Reid
Journal:  Clin Chest Med       Date:  1983-05       Impact factor: 2.878

9.  Contractile proteins in pericytes. I. Immunoperoxidase localization of tropomyosin.

Authors:  N C Joyce; M F Haire; G E Palade
Journal:  J Cell Biol       Date:  1985-05       Impact factor: 10.539

10.  Localization of myosin, actin, and tropomyosin in rat intestinal epithelium: immunohistochemical studies at the light and electron microscope levels.

Authors:  D Drenckhahn; U Gröschel-Stewart
Journal:  J Cell Biol       Date:  1980-08       Impact factor: 10.539

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  120 in total

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Review 5.  Molecular aspects of pathological processes in the artery wall.

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Review 9.  Neurovascular unit: a focus on pericytes.

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Journal:  Mol Neurobiol       Date:  2012-02-28       Impact factor: 5.590

Review 10.  Cerebral blood flow regulation and neurovascular dysfunction in Alzheimer disease.

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Journal:  Nat Rev Neurosci       Date:  2017-05-18       Impact factor: 34.870

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