Growth, morphogenesis, and differentiation during mouse prostate development in situ, in renal grafts, and in vitro

被引:30
作者
Doles, JD
Vezina, CM
Lipinski, RJ
Peterson, RE
Bushman, W
机构
[1] Univ Wisconsin, Dept Surg, Madison, WI 53792 USA
[2] Univ Wisconsin, Sch Pharm, Madison, WI 53706 USA
关键词
urogenital sinus; development; allograft; organ culture; differentiation;
D O I
10.1002/pros.20321
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: In vitro organ culture and renal grafting of the urogenital sinus (UGS) have both been used as models of prostate development. However, neither has been rigorously examined for its fidelity to replicate the canonical process of prostate differentiation in situ. METHODS: We assessed size, morphology, histology, and the mRNA expression of differentiation marker genes of the E14 male mouse UGS grown for 0-28 days as sub-renal capsule allografts, in nude mice or in culture containing androgen and compared these to UGS development in situ. RESULTS: Development of grafted tissues was morphologically and histologically similar to development in situ but differentiation occurred more rapidly. UGS growth in organ culture resulted in bud formation, but did not trigger cellular differentiation. However, the potential for differentiation was maintained and could be rescued by grafting tissues into nude mice. CONCLUSIONS: In vitro organ culture and renal grafting of UGS tissues may be appropriate models for studying prostatic bud formation, but only grafting is an appropriate model for prostatic differentiation.
引用
收藏
页码:390 / 399
页数:10
相关论文
共 38 条
[1]   THE COURSE OF NEURO-ENDOCRINE DIFFERENTIATION IN PROSTATIC CARCINOMAS - AN IMMUNOHISTOCHEMICAL STUDY TESTING CHROMOGRANIN-A AS AN ENDOCRINE MARKER [J].
ABRAHAMSSON, PA ;
FALKMER, S ;
FALT, K ;
GRIMELIUS, L .
PATHOLOGY RESEARCH AND PRACTICE, 1989, 185 (03) :373-380
[2]  
BRODY J, 1998, RENAL CAPSULE GRAFTI
[3]   Regulation of prostate branching morphogenesis by activin A and follistatin [J].
Cancilla, B ;
Jarred, RA ;
Wang, H ;
Mellor, SL ;
Cunha, GR ;
Risbridger, GP .
DEVELOPMENTAL BIOLOGY, 2001, 237 (01) :145-158
[4]   Disrupted gonadogenesis and male-to-female sex reversal in Pod1 knockout mice [J].
Cui, SY ;
Ross, A ;
Stallings, N ;
Parker, KL ;
Capel, B ;
Quaggin, SE .
DEVELOPMENT, 2004, 131 (16) :4095-4105
[5]   Hormonal, cellular, and molecular regulation of normal and neoplastic prostatic development [J].
Cunha, GR ;
Ricke, W ;
Thomson, A ;
Marker, PC ;
Risbridger, G ;
Hayward, SW ;
Wang, YZ ;
Donjacour, AA ;
Kurita, T .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2004, 92 (04) :221-236
[6]   STROMAL-EPITHELIAL INTERACTIONS IN SEX-DIFFERENTIATION [J].
CUNHA, GR ;
CHUNG, LWK ;
SHANNON, JM ;
REESE, BA .
BIOLOGY OF REPRODUCTION, 1980, 22 (01) :19-42
[7]   THE ENDOCRINOLOGY AND DEVELOPMENTAL BIOLOGY OF THE PROSTATE [J].
CUNHA, GR ;
DONJACOUR, AA ;
COOKE, PS ;
MEE, S ;
BIGSBY, RM ;
HIGGINS, SJ ;
SUGIMURA, Y .
ENDOCRINE REVIEWS, 1987, 8 (03) :338-362
[8]  
CUNHA GR, 1975, ENDOCRINOLOGY, V95, P665
[9]   IMMUNOCYTOCHEMICAL COMPARISON OF CULTURED NORMAL EPITHELIAL PROSTATIC CELLS WITH PROSTATIC TISSUE-SECTIONS [J].
CUSSENOT, O ;
BERTHON, P ;
COCHANDPRIOLLET, S ;
MAITLAND, NJ ;
LEDUC, A .
EXPERIMENTAL CELL RESEARCH, 1994, 214 (01) :83-92
[10]   FGF-10 plays an essential role in the growth of the fetal prostate [J].
Donjacour, AA ;
Thomson, AA ;
Cunha, GR .
DEVELOPMENTAL BIOLOGY, 2003, 261 (01) :39-54