Expression and function of laminins in the embryonic and mature vasculature

被引:415
作者
Hallmann, R
Horn, N
Selg, M
Wendler, O
Pausch, F
Sorokin, LM [1 ]
机构
[1] Lund Univ, SE-22185 Lund, Sweden
[2] Univ Erlangen Nurnberg, Interdisciplinary Ctr Clin Res, Erlangen, Germany
关键词
D O I
10.1152/physrev.00014.2004
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Expression and Function of Laminins in the Embryonic and Mature Vasculature. Physiol Rev 85: 979 - 1000, 2005; doi: 10.1152/ physrev.00014.2004. - Endothelial cells of the blood and lymphatic vasculature are polarized cells with luminal surfaces specialized to interact with inflammatory cells upon the appropriate stimulation; they contain specialized transcellular transport systems, and their basal surfaces are attached to an extracellular basement membrane. In adult tissues the basement membrane forms a continuous sleeve around the endothelial tubes, and the interaction of endothelial cells with basement membrane components plays an important role in the maintenance of vessel wall integrity. During development, the basement membrane of endothelium provides distinct spatial and molecular information that influences endothelial cell proliferation, migration, and differentiation/maturation. Microvascular endothelium matures into phenotypically distinct types: continuous, fenestrated, and discontinuous, which also differ in their permeability properties. Development of these morphological and physiological differences is thought to be controlled by both soluble factors in the organ or tissue environment and by cell-cell and cell-matrix interactions. Basement membranes of endothelium, like those of other tissues, are composed of laminins, type IV collagens, heparan sulfate proteoglycans, and nidogens. However, isoforms of all four classes of molecules exist, which combine to form structurally and functionally distinct basement membranes. The endothelial cell basement membranes have been shown to be unique with respect to their laminin isoform composition. Laminins are a family of glycoprotein heterotrimers composed of an alpha, beta, and gamma chain. To date, 5 alpha, 4 alpha, and 3 alpha laminin chains have been identified that can combine to form 15 different isoforms. The laminin alpha-chains are considered to be the functionally important portion of the heterotrimers, as they exhibit tissue-specific distribution patterns and contain the major cell interaction sites. Vascular endothelium expresses only two laminin isoforms, and their expression varies depending on the developmental stage, vessel type, and the activation state of the endothelium. Laminin 8 (composed of laminin alpha 4, beta 1, and gamma 1 chains) is expressed by all endothelial cells regardless of their stage of development, and its expression is strongly upregulated by cytokines and growth factors that play a role in inflammatory events. Laminin 10 (composed of laminin alpha 5, beta 1, and gamma 1 chains) is detectable primarily in endothelial cell basement membranes of capillaries and venules commencing 3 - 4 wk after birth. In contrast to laminin 8, endothelial cell expression of laminin 10 is upregulated only by strong proinflammatory signals and, in addition, angiostatic agents such as progesterone. Other extracellular matrix molecules, such as BM40 (also known as SPARC/osteonectin), thrombospondins 1 and 2, fibronectin, nidogens 1 and 2, and collagen types VIII, XV, and XVIII, are also differentially expressed by endothelium, varying with the endothelium type and/or pathophysiological state. The data argue for a dynamic endothelial cell extracellular matrix that presents different molecular information depending on the type of endothelium and/or physiological situation. This review outlines the unique structural and functional features of vascular basement membranes, with focus on the endothelium and the laminin family of glycoproteins.
引用
收藏
页码:979 / 1000
页数:22
相关论文
共 210 条
[1]  
Adams J, 2004, INT J BIOCHEM CELL B, V36, P960, DOI 10.1016/j.biocel.2004.02.009
[2]   Thrombospondins: Multifunctional regulators of cell interactions [J].
Adams, JC .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2001, 17 :25-51
[3]   Roles of ephrinB ligands and EphB receptors in cardiovascular development: demarcation of arterial/venous domains, vascular morphogenesis, and sprouting angiogenesis [J].
Adams, RH ;
Wilkinson, GA ;
Weiss, C ;
Diella, F ;
Gale, NW ;
Deutsch, U ;
Risau, W ;
Klein, R .
GENES & DEVELOPMENT, 1999, 13 (03) :295-306
[4]   Vascular bed-specific expression of an endothelial cell gene is programmed by the tissue microenvironment [J].
Aird, WC ;
Edelberg, JM ;
WeilerGuettler, H ;
Simmons, WW ;
Smith, TW ;
Rosenberg, RD .
JOURNAL OF CELL BIOLOGY, 1997, 138 (05) :1117-1124
[5]   THE CRANIAL ARACHNOID AND PIA MATER IN MAN - ANATOMICAL AND ULTRASTRUCTURAL OBSERVATIONS [J].
ALCOLADO, R ;
WELLER, RO ;
PARRISH, EP ;
GARROD, D .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1988, 14 (01) :1-17
[6]   CONGENITAL MUSCULAR-DYSTROPHIES [J].
ARAHATA, K ;
ISHII, H ;
HAYASHI, YK .
CURRENT OPINION IN NEUROLOGY, 1995, 8 (05) :385-390
[7]   Extensive vasculogenesis, angiogenesis, and organogenesis precede lethality in mice lacking all αv integrins [J].
Bader, BL ;
Rayburn, H ;
Crowley, D ;
Hynes, RO .
CELL, 1998, 95 (04) :507-519
[8]   Expression and regulation of the prokineticins (endocrine gland-derived vascular endothelial growth factor and Bv8) and their receptors in the human endometrium across the menstrual cycle [J].
Battersby, S ;
Critchley, HOD ;
Morgan, K ;
Millar, RP ;
Jabbour, HN .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (05) :2463-2469
[9]   STRUCTURE AND FUNCTION OF LAMININ - ANATOMY OF A MULTIDOMAIN GLYCOPROTEIN [J].
BECK, K ;
HUNTER, I ;
ENGEL, J .
FASEB JOURNAL, 1990, 4 (02) :148-160
[10]   Functions of cell surface heparan sulfate proteoglycans [J].
Bernfield, M ;
Götte, M ;
Park, PW ;
Reizes, O ;
Fitzgerald, ML ;
Lincecum, J ;
Zako, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1999, 68 :729-777