Glomerular Extracellular Matrix Components and Integrins
- 1 January 1998
- journal article
- research article
- Published by Taylor & Francis in Cell Adhesion and Communication
- Vol. 5 (3) , 177-192
- https://doi.org/10.3109/15419069809040290
Abstract
It has become apparent that extracellular matrix components and their cellular receptors, the integrins, are important regulators of glomerular development and function. In this rapidly evolving field we studied the production of extracellular matrix components and integrins by rat glomerular visceral epithelial and mesangial cells, using molecular probes and antibodies that have recently become available. Special attention was paid to laminin isoforms and to splice variants of the integrin subunits α3 and α6. Results were compared to the in vivo expression in human fetal, newborn and adult kidneys. The mesangial cells were found to produce laminin-1, nidogen and two as yet unidentified laminin isoforms with putative α chains of about 395 (m) and of 375 kDa (cry), tentatively described before as bovine kidney laminin. Furthermore, they expressed the integrins α1β1, α2β, α3Aβ1, α5β1, αvβ3, αvβ5, and small amounts of α6Aβ1 and α6Bβ1. The glomerular visceral epithelial cells produced the two new laminin isoforms mentioned above, laminin-5, but no laminin-1 or nidogen. The integrins α2β1, αAβ1, α6Aβ4, αBβ4 and the integrin subunit av were found to be expressed. We show that during nephrogenesis, the laminin α1 chain disappears and is replaced by another a chain, possibly one of the two as yet unidentified α chains mentioned above. The laminin β1 chain is replaced by the β2 chain somewhat later in glomerular development. In general, the integrins found to be expressed in glomeruli of adult kidney were consistent with those found in cultured glomerular visceral epithelial and mesangial cells. No splice variant switch of the integrin α3 or α6 subunits could be demonstrated during nephrogenesis. Our results suggest an important role for the mesangial cell in providing nidogen as a crucial component of the supramolecular stucture of the glomerular basement membrane. Furthermore our results indicate that laminin αxβ2γ1 and αβ2γ1 isoforms are important in the glomerulus of adult kidney and that the integrin α3Aβ1 is the main integrin receptor for laminin isoforms on glomerular visceral epithelial and mesangial cells, both in vitro and in vivo.Keywords
This publication has 53 references indexed in Scilit:
- Distribution of Laminin Variants and Their Integrin Receptors in Human Secondary Lymphoid Tissue: Colocalization suggests that the α6β4-integrin is a receptor for laminin-5 in lymphoid folliclesCell Adhesion and Communication, 1996
- The Human Integrin α8β1 Functions as a Receptor for Tenascin, Fibronectin, and VitronectinPublished by Elsevier ,1995
- Cloning and Complete Primary Structure of the Mouse Laminin α3 ChainPublished by Elsevier ,1995
- Novel Isoform of β1 Integrin Expressed in Skeletal and Cardiac MuscleBiochemical and Biophysical Research Communications, 1995
- Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches.The Journal of cell biology, 1994
- Distinct and overlapping ligand specificities of the alpha 3A beta 1 and alpha 6A beta 1 integrins: recognition of laminin isoforms.Molecular Biology of the Cell, 1994
- Characterization of native laminin from bovine kidney and comparison with other laminin variantsEuropean Journal of Biochemistry, 1994
- Integrins: Versatility, modulation, and signaling in cell adhesionCell, 1992
- The alpha 1-alpha 6 subunits of integrins are characteristically expressed in distinct segments of developing and adult human nephron.The Journal of cell biology, 1990
- A simple method for the quantitative isolation of undegraded high molecular weight ribonucleic acidBiochemical and Biophysical Research Communications, 1963