Embryonic renal epithelia: Induction, nephrogenesis, and cell differentiation

被引:158
作者
Horster, MF [1 ]
Braun, GS [1 ]
Huber, SM [1 ]
机构
[1] Univ Munich, Inst Physiol, D-80336 Munich, Germany
关键词
D O I
10.1152/physrev.1999.79.4.1157
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Embryonic metanephroi, differentiating into the adult kidney, have come to be a generally accepted model system for organogenesis. Nephrogenesis implies a highly controlled series of morphogenetic and differentiation events that starts with reciprocal inductive interactions between two different primordial tissues and leads, in one of two mainstream processes, to the formation of mesenchymal condensations and aggregates. These go through the intricate process of mesenchyme-to-epithelium transition by which epithelial cell polarization is initiated, and they continue to differentiate into the highly specialized epithelial cell populations of the nephron. Each step along the developmental metanephrogenic pathway is initiated and organized by signaling molecules that are locally secreted polypeptides encoded by different gene families and regulated by transcription factors. Nephrogenesis proceeds from the deep to the outer cortex, and it is directed by a second, entirely different developmental process, the ductal branching of the ureteric bud-derived collecting tubule. Both systems, the nephrogenic (mesenchymal) and the ductogenic (urcteric), undergo a repeat series of inductive signaling that serves to organize the architecture and differentiated cell functions in a cascade of developmental gene programs. The aim of this review is to present a coherent picture of principles and mechanisms in embryonic renal epithelia.
引用
收藏
页码:1157 / 1191
页数:35
相关论文
共 307 条
[31]   APOPTOSIS AND EXPRESSION OF THE BCL-2 PROTOONCOGENE IN THE FETAL AND ADULT HUMAN KIDNEY - EVIDENCE FOR THE CONTRIBUTION OF BCL-2 EXPRESSION TO RENAL CARCINOGENESIS [J].
CHANDLER, D ;
ELNAGGAR, AK ;
BRISBAY, S ;
REDLINE, RW ;
MCDONNELL, TJ .
HUMAN PATHOLOGY, 1994, 25 (08) :789-796
[32]   EMBRYONIC LETHALITY IN MICE HOMOZYGOUS FOR A TARGETED DISRUPTION OF THE N-MYC GENE [J].
CHARRON, J ;
MALYNN, BA ;
FISHER, P ;
STEWART, V ;
JEANNOTTE, L ;
GOFF, SP ;
ROBERTSON, EJ ;
ALT, FW .
GENES & DEVELOPMENT, 1992, 6 (12A) :2248-2257
[33]  
CHEN JM, 1991, ONCOGENE, V6, P257
[34]  
CHOI ME, 1997, AM J PHYSIOL, V273, pF368
[35]  
COLES HSR, 1993, DEVELOPMENT, V118, P777
[36]  
Cook DM, 1996, ONCOGENE, V13, P1789
[37]   THE FORMATION OF THE PRONEPHRIC DUCT IN XENOPUS INVOLVES RECRUITMENT OF POSTERIOR CELLS BY MIGRATING PRONEPHRIC DUCT CELLS [J].
CORNISH, JA ;
ETKIN, LD .
DEVELOPMENTAL BIOLOGY, 1993, 159 (01) :338-345
[38]   Distribution of alpha-integrin subunits in fetal polycystic kidney diseases [J].
DaikhaDahmane, F ;
Narcy, F ;
Dommergues, M ;
Lacoste, M ;
Beziau, A ;
Gubler, MC .
PEDIATRIC NEPHROLOGY, 1997, 11 (03) :267-273
[39]   The cystic fibrosis transmembrane conductance regulator mediates transepithelial fluid secretion by human autosomal dominant polycystic kidney disease epithelium in vitro [J].
Davidow, CJ ;
Maser, RL ;
Rome, LA ;
Calvet, JP ;
Grantham, JJ .
KIDNEY INTERNATIONAL, 1996, 50 (01) :208-218
[40]  
DAVIES J, 1995, DEVELOPMENT, V121, P1507