Immunohistochemical identification of arteriolar development using markers of smooth muscle differentiation. Evidence that capillary arterialization proceeds from terminal arterioles.
- 1 September 1994
- journal article
- abstracts
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 75 (3) , 520-527
- https://doi.org/10.1161/01.res.75.3.520
Abstract
Arteriolar growth is an important event in the adaptation of normal tissues as well as in important pathologies, but the site of origin of new arterioles remains unknown. The network pattern of arteriolar development in skeletal muscle was detected by use of a new immunohistochemical technique that is based on the observation that fully differentiated (mature) vascular smooth muscle (SM) cells express both SM alpha-actin and the two myosin heavy chains (MHCs) SM-1 and SM-2, whereas less differentiated (immature) vascular SM cells do not express MHC. The anterior gracilis muscle microvasculatures of 4- and 9-week-old Sprague-Dawley rats were labeled with monoclonal antibodies to SM alpha-actin and to SM MHC. Whole transverse arteriole networks were observed, and terminal arterioles, defined as terminal segments labeled with SM alpha-actin, were classified on the basis of the presence or absence of SM MHC. A significantly different percentage of terminal arteriolar endings per network without SM MHC was observed in the two groups (66.1 +/- 17.3% for 4 weeks and 27.1 +/- 18.5% for 9 weeks), suggesting that arteriolar development is more nearly complete in the older animals. Sparsely distributed capillaries exhibited thin extensions of SM alpha-actin that crossed collecting venules and joined similar extensions from an adjacent transverse arteriole, effectively forming the basis for new arcade arterioles. SM alpha-actin and SM MHC labeling in terminal arterioles was always continuous with upstream arterioles.(ABSTRACT TRUNCATED AT 250 WORDS)Keywords
This publication has 15 references indexed in Scilit:
- Circumferential Wall Stress as a Mechanism for Arteriolar Rarefaction and Proliferation in a Network ModelMicrovascular Research, 1994
- Phenotypic changes of human smooth muscle cells during development: Late expression of heavy caldesmon and calponinDevelopmental Biology, 1992
- Heterogeneity of microvascular pericytes for smooth muscle type alpha-actin.The Journal of cell biology, 1991
- Microvascular and collateral adaptation in swine hearts following progressive coronary artery stenosisBasic Research in Cardiology, 1989
- Myosin heavy‐chain isoforms in adult and developing rabbit vascular smooth muscleEuropean Journal of Biochemistry, 1989
- Griffonia simplicifolia I: Fluorescent tracer for microcirculatory vessels in nonperfused thin muscles and sectioned muscleMicrovascular Research, 1988
- A monoclonal antibody against alpha-smooth muscle actin: a new probe for smooth muscle differentiation.The Journal of cell biology, 1986
- Contractile proteins in pericytes. II. Immunocytochemical evidence for the presence of two isomyosins in graded concentrations.The Journal of cell biology, 1985
- Arteriolar proliferation in the rat cremaster muscle as a long-term autoregulatory response to reduced perfusionMicrovascular Research, 1984
- Actin Typing on Total Cellular ExtractsEuropean Journal of Biochemistry, 1981