Literature DB >> 1116230

Intimal injury and regrowth in the rabbit aorta; medial smooth muscle cells as a source of neointima.

T H Spaet, M B Stemerman, F J Veith, I Lejnieks.   

Abstract

The present study was undertaken to determine the mechanism of neointima formation in rabbit arteries subjected to extensive endothelial desquamation. Endothelial cells were selectively removed from the abdominal aorta by passing an inflated balloon catheter through the vessel. The healing response was then studied serially for up to a week, when neointima formation had provided a virtually complete cover. In en face preparations, the early neointimal cells appeared in random locations; they did not develop in apposition to residual, healthy endothelium. The possibility of blood cell colonization was explored by inserting killed aortic homografts. Since these homografts showed neointima formation only close to the site of junction with the normal aorta and as a direct extension of healthy endothelium, the likelihood of significant blood cell colonization was deemed small. Histologic and electron microscopic sections provided evidence that the early neointimal cells in the healing aorta were derived from medial smooth muscle cells. Healing of the injured arterial intima was accompanied by thickening instead of prompt restoration to normal, and the thickened intima resembled an arteriosclerotic plaque. The present study thus supports the concept that arteriosclerosis is a disease involving proliferation of medial smooth muscle cells.

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Year:  1975        PMID: 1116230     DOI: 10.1161/01.res.36.1.58

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  32 in total

1.  Dynamics of Vascular Remodeling: An Overview and Bibliography.

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2.  Topographical and ultrastructural alterations of smooth muscle cells lining damaged rabbit aorta.

Authors:  C H Ts'ao
Journal:  Br J Exp Pathol       Date:  1975-08

3.  Enzyme activities in endothelial cells and smooth muscle cells from swine aorta.

Authors:  L W Hayes; C A Goguen; A L Stevens; W W Magargal; L L Slakey
Journal:  Proc Natl Acad Sci U S A       Date:  1979-06       Impact factor: 11.205

4.  Estradiol attenuates directed migration of vascular smooth muscle cells in vitro.

Authors:  F D Kolodgie; A Jacob; P S Wilson; G C Carlson; A Farb; A Verma; R Virmani
Journal:  Am J Pathol       Date:  1996-03       Impact factor: 4.307

5.  Deendothelialization in vivo initiates a thrombogenic reaction at the rabbit aorta surface. Correlation of uptake of fibrinogen and antithrombin III with thrombin generation by the exposed subendothelium.

Authors:  M W Hatton; S L Moar; M Richardson
Journal:  Am J Pathol       Date:  1989-09       Impact factor: 4.307

Review 6.  Current understanding of intimal hyperplasia and effect of compliance in synthetic small diameter vascular grafts.

Authors:  YeJin Jeong; Yuan Yao; Evelyn K F Yim
Journal:  Biomater Sci       Date:  2020-07-09       Impact factor: 6.843

7.  Time course of arterial repair following endothelial denudation in the rat carotid artery. A morphometric study in Wistar and Sprague-Dawley rats.

Authors:  E van Pelt-Verkuil; J Knoester; W van Pelt; M Brink; D Jense; J J Emeis
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1986

Review 8.  Vein graft failure.

Authors:  Christopher D Owens; Warren J Gasper; Amreen S Rahman; Michael S Conte
Journal:  J Vasc Surg       Date:  2013-10-03       Impact factor: 4.268

9.  Macromolecular synthesis in the isolated rat myointima in vitro.

Authors:  J F Hartmann; S L Chen; G S Young
Journal:  Am J Pathol       Date:  1990-06       Impact factor: 4.307

10.  Endothelial regeneration. VII. Lack of intimal proliferation after defined injury to rat aorta.

Authors:  M A Reidy; M Silver
Journal:  Am J Pathol       Date:  1985-02       Impact factor: 4.307

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