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.
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页码:1157 / 1191
页数:35
相关论文
共 307 条
[11]   DIFFERENTIAL TUBULOGENIC AND BRANCHING MORPHOGENETIC ACTIVITIES OF GROWTH-FACTORS - IMPLICATIONS FOR EPITHELIAL TISSUE-DEVELOPMENT [J].
BARROS, EJG ;
SANTOS, OFP ;
MATSUMOTO, K ;
NAKAMURA, T ;
NIGAM, SK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (10) :4412-4416
[12]   ONTOGENY OF RABBIT RENAL CORTICAL NHE3 AND NHE1 - EFFECT OF GLUCOCORTICOIDS [J].
BAUM, M ;
BIEMESDERFER, D ;
GENTRY, D ;
ARONSON, PS .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1995, 268 (05) :F815-F820
[13]   CHARACTERIZATION OF THE FETAL GLUCOSE TRANSPORTER IN RABBIT KIDNEY - COMPARISON WITH THE ADULT BRUSH-BORDER ELECTROGENIC NA+-GLUCOSE SYMPORTER [J].
BECK, JC ;
LIPKOWITZ, MS ;
ABRAMSON, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (02) :379-387
[14]  
Bernardini N, 1996, DEV DYNAM, V206, P231, DOI 10.1002/(SICI)1097-0177(199607)206:3<231::AID-AJA1>3.0.CO
[15]  
2-J
[16]   SYNDECAN, A DEVELOPMENTALLY REGULATED CELL-SURFACE PROTEOGLYCAN THAT BINDS EXTRACELLULAR-MATRIX AND GROWTH-FACTORS [J].
BERNFIELD, M ;
SANDERSON, RD .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1990, 327 (1239) :171-186
[17]   MODULATION OF DNA-BINDING SPECIFICITY BY ALTERNATIVE SPLICING OF THE WILMS-TUMOR WT1 GENE TRANSCRIPT [J].
BICKMORE, WA ;
OGHENE, K ;
LITTLE, MH ;
SEAWRIGHT, A ;
VANHEYNINGEN, V ;
HASTIE, ND .
SCIENCE, 1992, 257 (5067) :235-237
[18]   MOLECULAR ASPECTS OF MESENCHYMAL-EPITHELIAL INTERACTIONS [J].
BIRCHMEIER, C ;
BIRCHMEIER, W .
ANNUAL REVIEW OF CELL BIOLOGY, 1993, 9 :511-540
[19]   APOPTOTIC CELL-DEATH INDUCED BY C-MYC IS INHIBITED BY BCL-2 [J].
BISSONNETTE, RP ;
ECHEVERRI, F ;
MAHBOUBI, A ;
GREEN, DR .
NATURE, 1992, 359 (6395) :552-554
[20]   HEDGEHOG AND BMP GENES ARE COEXPRESSED AT MANY DIVERSE SITES OF CELL-CELL INTERACTION IN THE MOUSE EMBRYO [J].
BITGOOD, MJ ;
MCMAHON, AP .
DEVELOPMENTAL BIOLOGY, 1995, 172 (01) :126-138