Accumulation and Loss of Extracellular Matrix During Shear Stress-mediated Intimal Growth and Regression in Baboon Vascular Grafts

Author:

Kenagy Richard D.1,Fischer Jens W.2,Lara Stephanie3,Sandy John D.4,Clowes Alexander W.13,Wight Thomas N.5

Affiliation:

1. Department of Vascular Surgery, University of Washington, Seattle, Washington

2. Molecular Pharmacology, Institute of Pharmacology and Clinical Pharmacology, Heinrich-Heine-University, Düsseldorf, Germany

3. Department of Pathology, University of Washington, Seattle, Washington

4. Shriners Hospital and Department of Pharmacology, University of South Florida, Tampa, Florida

5. The Hope Heart Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington

Abstract

The composition of extracellular matrix during growth and regression of the neointima was analyzed during healing in a baboon aortoiliac polytetrafluoroethylene graft. Graft neointimal thickening can be modulated by altering blood flow by construction of downstream arteriovenous fistulas. Normal flow with normal shear stress induces neointimal thickening, whereas high flow with high shear stress upstream of a fistula induces regression of established neointima. The neointima formed under normal shear stress is enriched in hyaluronan and proteoglycans, particularly versican. On the other hand, the neointima near the graft material is enriched in collagen and biglycan. Neointimal regression in response to high shear stress is associated with a loss of proteoglycans as detected by histochemical staining. Immunostaining with an antibody against an ADAMTS cleavage neoepitope of versican increases after switching to high flow, although immunostaining for versican core protein is not appreciably changed by high flow. The present data demonstrate that the graft neointima is enriched with proteoglycans, particularly versican and hyaluronan, as well as collagen, and there is a differential distribution of each. Neointimal atrophy occurs with an apparent loss of proteoglycans and evidence of versican degradation.

Publisher

SAGE Publications

Subject

Histology,Anatomy

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1. Microfibrillar-associated protein 4 in health and disease;Matrix Biology;2022-08

2. Versican in Tumor Progression, Tumor–Host Interactions, and Cancer Immunotherapy;The Extracellular Matrix and the Tumor Microenvironment;2022

3. Extracellular Matrix in Vascular Disease, Part 2/4;Journal of the American College of Cardiology;2020-05

4. ADAMTS‐5: A difficult teenager turning 20;International Journal of Experimental Pathology;2020-02

5. A simple ex vivo model of human renal allograft preservation using the gonadal vein;The Annals of The Royal College of Surgeons of England;2019-11

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