Growth of arterioles precedes that of capillaries in stretch-induced angiogenesis in skeletal muscle.

Arteriolar growth accompanying capillary angiogenesis has been linked with hemodynamic factors resulting from increased blood flow. Here we describe the growth of arterioles occurring in rat skeletal muscles stretched by an overload due to the removal of agonist muscles, where blood flow was not increased, and we provide morphological evidence for the type of cells involved in this growth. Rat extensor digitorum longus (EDL) and extensor hallucis proprius (EHP) were overloaded by unilateral extirpation of their agonist, tibialis anterior. EDL muscles were taken for immunohistochemistry in cryostat sections to mark endothelial cells (Griffonia simplicifolia I, GSI lectin), smooth muscle cells and pericytes (alpha smooth muscle actin, alphaSMA), and "mature" arterioles (smooth muscle myosin heavy chains). EHP muscles were used for corresponding evaluation by confocal and electron microscopy. The number of capillaries surrounding muscle fibers was not significantly different after 1 week of stretch but was higher after 2 weeks (5.15 +/- 0.2 vs 4.3 +/- 0.2 in controls, P < 0.05). Similarly, capillary density (CD) and capillary/fiber ratio (C/F) gradually increased (CD 778 +/- 86 at 2 weeks vs 593 +/- 35 mm(-2) in controls, C/F 2.07 +/- 0.13 vs 1.38 +/- 0.06, respectively). In contrast, the number of alphaSMA-positive vessels around fibers increased after 1 week (2.16 +/- 0.09 vs 0.25 +/- 0.02 in controls) and was lower after 2 weeks (1.42 +/- 0.24, P < 0.05, vs 1 week). Arteriolar density was higher at 1 (110.9 +/- 7.5 mm(-2)) and 2 weeks (70.7 +/- 12.1) with respect to controls (31.0 +/- 1.6 mm(-2)). The increased density was greater in alphaSMA-positive vessels <10 microm in diameter (controls 18.0 +/- 1.04, 1 week 77.2 +/- 4.5, 2 wk 42.2 +/- 9.0 mm(-2)) than in vessels >10 microm (13.0 +/- 0.8, 33.7 +/- 4.0, 29.5 +/- 4.7 mm(-2)). Electron microscopy showed "activated" (TEM fine structure) and proliferating (immunogold labeling for BrdU) fibroblasts in the vicinity of capillaries, some of which were embedded in the capillary basement membrane, consistent with a transformation into pericytes and possibly later smooth muscle cells. Confocal microscopy indicated that some mesenchymal cells became GSI positive and formed extended processes which contacted capillaries via tapered endings. Growth of arterioles in stretched muscles appears to involve proliferation of fibroblasts, which may migrate toward capillaries and precedes any apparent increase in capillarization.

[1]  A L Zhou,et al.  Capillary growth in overloaded, hypertrophic adult rat skeletal muscle: An ultrastructural study , 1998, The Anatomical record.

[2]  T. Skalak,et al.  Where Do New Arterioles Come From? Mechanical Forces and Microvessel Adaptation , 1998, Microcirculation.

[3]  S. Egginton,et al.  The role of pericytes in controlling angiogenesis in vivo. , 2000, Advances in experimental medicine and biology.

[4]  Richard Thoma,et al.  Untersuchungen über die Histogenese und Histomechanik des Gefässsystems , 1894 .

[5]  D. Poole,et al.  In vivo microvascular structural and functional consequences of muscle length changes. , 1997, The American journal of physiology.

[6]  R. Weiss,et al.  Mechanical strain induces growth of vascular smooth muscle cells via autocrine action of PDGF , 1993, The Journal of cell biology.

[7]  A. Ziada,et al.  The effect of long-term vasodilatation on capillary growth and performance in rabbit heart and skeletal muscle. , 1984, Cardiovascular research.

[8]  C. Bloor,et al.  Exercise training in swine promotes growth of arteriolar bed and capillary angiogenesis in heart. , 1998, Journal of applied physiology.

[9]  A Kamiya,et al.  The effect of fluid shear stress on the migration and proliferation of cultured endothelial cells. , 1986, Microvascular research.

[10]  S. Izumo,et al.  Fluid shear stress differentially modulates expression of genes encoding basic fibroblast growth factor and platelet-derived growth factor B chain in vascular endothelium. , 1993, The Journal of clinical investigation.

[11]  Qingbo Xu,et al.  Activation of PDGF receptor α in vascular smooth muscle cells by mechanical stress , 1998 .

[12]  T. Skalak,et al.  Immunohistochemical identification of arteriolar development using markers of smooth muscle differentiation. Evidence that capillary arterialization proceeds from terminal arterioles. , 1994, Circulation research.

[13]  S. Egginton,et al.  In vivo angiogenesis in adult rat skeletal muscle: early changes in capillary network architecture and ultrastructure , 1996, Cell and Tissue Research.

[14]  Blood flow and glycogen use in hypertrophied rat muscles during exercise. , 1986, Journal of applied physiology.

[15]  S. Egginton,et al.  Capillary growth in relation to blood flow and performance in overloaded rat skeletal muscle. , 1998, Journal of applied physiology.

[16]  O. Hudlická Is Physiological Angiogenesis in Skeletal Muscle Regulated by Changes in Microcirculation? , 1998, Microcirculation.

[17]  N Wang,et al.  Mechanical interactions among cytoskeletal filaments. , 1998, Hypertension.

[18]  I. Goldstein,et al.  Griffonia simplicifolia I: fluorescent tracer for microcirculatory vessels in nonperfused thin muscles and sectioned muscle. , 1988, Microvascular research.

[19]  S. Egginton,et al.  Angiogenesis in skeletal and cardiac muscle. , 1992, Physiological reviews.

[20]  Mechanical stretch increases proto‐oncogene expression and phosphoinositide turnover in vascular smooth muscle cells , 1994, Journal of hypertension.

[21]  S. Egginton,et al.  Growth of Arterioles in Chronically Stimulated Adult Rat Skeletal Muscle , 1998, Microcirculation.

[22]  E. R. Clark,et al.  Microscopic observations on the extra‐endothelial cells of living mammalian blood vessels , 1940 .

[23]  H. Bohlen,et al.  Functional adaptations of rat skeletal muscle arterioles to aerobic exercise training. , 1992, Journal of applied physiology.

[24]  H. Yamashita,et al.  Effect of traction on the vasculature of chorioallantoic membranes of chick embryos. , 1989, Investigative ophthalmology & visual science.

[25]  T. Matsuda,et al.  Behavior of Arterial Wall Cells Cultured on Periodically Stretched Substrates , 1993, Cell transplantation.

[26]  R. Binkhorst,et al.  The relationship between capillarisation and fibre types during compensatory hypertrophy of the plantaris muscle in the rat. , 1992, Journal of anatomy.

[27]  O. Hudlická,et al.  Can changes in microcirculation explain capillary growth in skeletal muscle? , 1993, International journal of experimental pathology.

[28]  S. Egginton,et al.  In VivoPericyte–Endothelial Cell Interaction during Angiogenesis in Adult Cardiac and Skeletal Muscle , 1996 .

[29]  A. Papavassiliou,et al.  Mechanical stress induces DNA synthesis in PDL fibroblasts by a mechanism unrelated to autocrine growth factor action , 1998, FEBS letters.

[30]  M. Conte Angiogenesis: From the molecular to integrative pharmacology , 2002 .

[31]  J. R. Coelho,et al.  Microvascular development in chick anterior latissimus dorsi following hypertrophy. , 1989, Journal of anatomy.

[32]  R. Bjercke,et al.  Bradycardia-induced coronary angiogenesis is dependent on vascular endothelial growth factor. , 1999, Circulation research.

[33]  Prazosin administration enhances proliferation of arteriolar adventitial fibroblasts. , 1998, Microvascular research.

[34]  N. James A stereological analysis of capillaries in normal and hypertrophic muscle , 1981, Journal of morphology.

[35]  J. Stingl Zur Ultrastruktur des terminalen Gefäβbettes der Skeletmuskulatur , 1971 .

[36]  S. Chien,et al.  Effects of mechanical forces on signal transduction and gene expression in endothelial cells. , 1998, Hypertension.

[37]  O. Hudlická,et al.  Postnatal growth of the heart and its blood vessels. , 1996, Journal of vascular research.

[38]  R. Taylor,et al.  Stretch-induced growth in chicken wing muscles: a new model of stretch hypertrophy. , 1980, The American journal of physiology.