Lessons from studies on focal segmental glomerulosclerosis: an important role for parietal epithelial cells?

被引:33
作者
Smeets, B.
Dijkman, H. B. P. M.
Wetzels, J. F. M.
Steenbergen, E. J.
机构
[1] Univ Nijmegen, Radboud Med Ctr, Dept Pathol, Nijmegen, Netherlands
[2] Univ Nijmegen, Radboud Med Ctr, Dept Nephrol, Nijmegen, Netherlands
关键词
parietal epithelial cell; podocyte; focal segmental glomerulosclerosis; collapsing FSGS;
D O I
10.1002/path.2051
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glomerular diseases are caused by multiple mechanisms. Progressive glomerular injury is characterized by the development of segmental or global glomerulosclerosis independent of the nature of the underlying renal disease. Most studies on glomerular disease focus on the constituents of the filtration barrier (podocytes, glomerular basement membrane (GBM), endothelial cells) or the mesangial cells. Little attention is given to the epithelial cells lining Bowman's capsule, the so called parietal epithelial cells (PECs). This 'lack of attention' is partly explained by the presumed 'passive' function of PECs, which are large, flattened cells that cover Bowman's capsule in a single cell layer and form a barrier between the ultrafiltrate and the periglomerular interstitium, in normal glomerular physiology. A more important reason has been the lack of an established primary role for the parietal epithelium in glomerular diseases. However, in recent years, several studies have demonstrated that PECs are involved in extracapillary proliferation. In addition, PECs can become highly active, proliferating cells, expressing many growth factors, chemokines, cytokines, and their receptors. It was recently demonstrated that PECs also play a part in the development of focal segmental glomerulosclerosis (FSGS). This review summarises current knowledge of the PEC, with emphasis on the role of PECs in the development of FSGS. Copyright (c) 2006 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:263 / 272
页数:10
相关论文
共 96 条
[1]   STRUCTURE AND DEVELOPMENT OF THE GLOMERULAR CAPILLARY WALL AND BASEMENT-MEMBRANE [J].
ABRAHAMSON, DR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (05) :F783-F794
[2]  
ALPERS CE, 1994, J AM SOC NEPHROL, V5, P201
[3]   Permanent genetic tagging of podocytes: Fate of injured podocytes in a mouse model of glomerular sclerosis [J].
Asano, T ;
Niimura, F ;
Pastan, I ;
Fogo, AB ;
Ichikawa, I ;
Matsusaka, T .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (08) :2257-2262
[4]  
Bariéty J, 2001, J AM SOC NEPHROL, V12, P261, DOI 10.1681/ASN.V122261
[5]   Podocytes undergo phenotypic changes and express macrophagic-associated markers in idiopathic collapsing glomerulopathy [J].
Bariéty, J ;
Nochy, D ;
Mandet, C ;
Jacquot, C ;
Glotz, D ;
Meyrier, A .
KIDNEY INTERNATIONAL, 1998, 53 (04) :918-925
[6]  
Barisoni L, 1999, J AM SOC NEPHROL, V10, P51
[7]  
BARNES JL, 1995, AM J PATHOL, V147, P1361
[8]   Podocyte injury associated glomerulopathies induced by pamidronate [J].
Barri, YM ;
Munshi, NC ;
Sukumalchantra, S ;
Abulezz, SR ;
Bonsib, SM ;
Wallach, J ;
Walker, PD .
KIDNEY INTERNATIONAL, 2004, 65 (02) :634-641
[9]  
BOUCHER A, 1987, LAB INVEST, V56, P526
[10]   NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome [J].
Boute, N ;
Gribouval, O ;
Roselli, S ;
Benessy, F ;
Lee, H ;
Fuchshuber, A ;
Dahan, K ;
Gubler, MC ;
Niaudet, P ;
Antignac, C .
NATURE GENETICS, 2000, 24 (04) :349-354