IDENTIFICATION OF SPECIFIC GLOMERULAR CELL-TYPES IN CULTURE BY USE OF LECTIN AND ANTIBODY-BINDING

被引:21
作者
HOLTHOFER, H [1 ]
DECANDIDO, S [1 ]
SCHLONDORFF, D [1 ]
机构
[1] YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT MED, DIV NEPHROL, BRONX, NY 10461 USA
来源
CELL DIFFERENTIATION AND DEVELOPMENT | 1990年 / 30卷 / 03期
关键词
Antibody; Endothelial cell; Epithelial cell; Glomerular culture; Lectin; Mesangial cell;
D O I
10.1016/0922-3371(90)90138-M
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To characterize the outgrowth of cells from cultured rat glomeruli, we examined the cell morphology in relation to the expression of various antigenic determinants (factor VIII-related antigen, rat Thy 1.1, Heyman nephritogenic antigen, common leucocyte and Ia antigens) and lectin binding patterns. For this purpose, early (3-7 days) to late (4-5 weeks) glomerulus cultures, as well as subcultures of mesangial cells were used. In the early samples, the predominance of small round (type I) cells growing in a cobblestone pattern was noted. These cells failed to express specific binding for any of the antibodies or lectins tested. 5-10% of the outgrowing cells appeared single and morphologically of stellate shape (type II). These cells were reactive for Concanavalia ensiformis (ConA), Triticum vulgaris (WGA) and Ricinus communis (RCA I), and stained for rat Thy 1.1 antigen. Large round, single cells (type III), found mostly at the edges of the outgrowth bound only Bandeiraea simplicifolia (BSI-B4) and FVIII antibodies, a pattern consistent with endothelial cells. A fourth (type IV) cell type, elongated, with cells mostly found in bundles and growing on a layer consisting of other cells, was reactive for ConA, WGA, Limax flavus (LFA) and Maclura pomifera (MPA) lectins. In the late outgrowth (3-5 weeks after explant), the lectin and antibody binding patterns of each cell type remained essentially unchanged. However, considerable changes in the prevalence of the morphologic cell types were noted. Cells that had been subcultured to obtain pure 'mesangial' cells, exhibited the same morphology as the type II cells and expressed identical staining patterns with all probes used. The binding of lectins was likewise confirmed by staining frozen sections of rat kidneys. © 1990 Elsevier Scientific Publishers Ireland, Ltd. All rights reserved.
引用
收藏
页码:181 / 194
页数:14
相关论文
共 44 条
[12]  
HOLTHOFER H, 1984, LAB INVEST, V50, P552
[13]  
HOLTHOFER H, 1981, LAB INVEST, V45, P391
[14]   Glycosylation of developing human glomeruli: Lectin binding sites during cell induction and maturation [J].
Holthofer, H. ;
Virtanen, I. .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1987, 35 (01) :33-37
[16]  
JAFFE EA, 1977, NEW ENGL J MED, V296, P377
[17]  
KANWAR YS, 1984, LAB INVEST, V51, P7
[18]   HUMAN GLOMERULAR VISCERAL EPITHELIAL-CELLS SYNTHESIZE A BASAL LAMINA COLLAGEN INVITRO [J].
KILLEN, PD ;
STRIKER, GE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (07) :3518-3522
[19]   GLOMERULAR CELLS IN CULTURE [J].
KREISBERG, JI ;
KARNOVSKY, MJ .
KIDNEY INTERNATIONAL, 1983, 23 (03) :439-447
[20]   GRIFFONIA-SIMPLICIFOLIA LECTINS BIND SPECIFICALLY TO ENDOTHELIAL-CELLS AND SOME EPITHELIAL-CELLS IN MOUSE-TISSUES [J].
LAITINEN, L .
HISTOCHEMICAL JOURNAL, 1987, 19 (04) :225-234