Topological determinants and consequences of adventitial responses to arterial wall injury

Arterioscler Thromb Vasc Biol. 2007 Jun;27(6):1259-68. doi: 10.1161/ATVBAHA.106.137851. Epub 2007 Mar 29.

Abstract

Arteries are composed of 3 concentric tissue layers which exhibit different structures and properties. Because arterial injury is generally initiated at the interface with circulating blood, most studies performed to unravel the mechanisms involved in injury-induced arterial responses have focused on the innermost layer (intima) rather than on the outermost adventitial layer. In the present review, we focus on the involvement of the adventitia in response to various types of arterial injury leading to vascular remodeling. Physiologically, soluble vascular mediators are centrifugally conveyed by mass transport toward the adventitia. Moreover, in pathological conditions, neomediators and antigens can be generated within the arterial wall, whose outward conveyance triggers different patterns of local adventitial response. Adventitial angiogenesis, immunoinflammation, and fibrosis sequentially interact and their net balance defines the participation of the adventitial response in arterial pathology. In the present review we discuss 4 pathological entities in which the adventitial response to arterial wall injury participates in arterial wall remodeling. Hence, the adventitial adaptive immune response predominates in chronic rejection. Inflammatory phagocytic cell recruitment and initiation of a shift from innate to adaptive immunity characterize the adventitial response to products of proteolysis in abdominal aortic aneurysm. Adventitial sprouting of neovessels, leading to intraplaque hemorrhages, predominates in atherothrombosis. Adventitial fibrosis characterizes the response to mechanical stress and is responsible for the constrictive remodeling of arterial segments and initiating interstitial fibrosis in perivascular tissues. These adventitial events, therefore, have an impact not only on the vessel wall biology but also on the surrounding tissue.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigens / metabolism
  • Aortic Aneurysm, Abdominal / immunology*
  • Aortic Aneurysm, Abdominal / metabolism
  • Aortic Aneurysm, Abdominal / pathology
  • Arteries / immunology
  • Arteries / injuries*
  • Arteries / metabolism
  • Arteries / pathology
  • Arteries / transplantation
  • Atherosclerosis / metabolism
  • Atherosclerosis / pathology*
  • Connective Tissue / blood supply
  • Connective Tissue / immunology
  • Connective Tissue / metabolism
  • Connective Tissue / pathology*
  • Connective Tissue / physiopathology
  • Fibrosis
  • Graft Rejection / immunology*
  • Graft Rejection / metabolism
  • Graft Rejection / pathology
  • Humans
  • Inflammation / immunology
  • Inflammation / metabolism
  • Inflammation / pathology
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Lymphoid Tissue / immunology
  • Lymphoid Tissue / pathology
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / pathology
  • Peptide Hydrolases / metabolism
  • Phagocytes / immunology
  • Stress, Mechanical
  • Tunica Intima / pathology
  • Tunica Media / pathology

Substances

  • Antigens
  • Intercellular Signaling Peptides and Proteins
  • Peptide Hydrolases