Proximal location of mouse prostate epithelial stem cells: a model of prostatic homeostasis

被引:242
作者
Tsujimura, A
Koikawa, Y
Salm, S
Takao, T
Coetzee, S
Moscatelli, D
Shapiro, E
Lepor, H
Sun, TT
Wilson, EL
机构
[1] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Urol, New York, NY 10016 USA
[3] NYU, Sch Med, Ronald O Perelman Dept Dermatol, New York, NY 10016 USA
[4] NYU, Sch Med, Dept Pharmacol, New York, NY 10016 USA
[5] NYU, Sch Med, Kaplan Canc Ctr, New York, NY 10016 USA
[6] Osaka Univ, Sch Med, Dept Urol, Suita, Osaka 5650871, Japan
[7] Fukuoka City Med Ctr Sick Children & Infect Dis, Dept Urol, Fukuoka 8100063, Japan
关键词
prostate; stem cells; slow-cycling cells; branching morphogenesis; prostate regeneration;
D O I
10.1083/jcb.200202067
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stem cells are believed to regulate normal prostatic homeostasis and to play a role in the etiology of prostate cancer and benign prostatic hyperplasia. We show here that the proximal region of mouse prostatic ducts is enriched in a subpopulation of epithelial cells that exhibit three important attributes of epithelial stem cells: they are slow cycling, possess a high in vitro proliferative potential, and can reconstitute highly branched glandular ductal structures in collagen gels. We propose a model of prostatic homeostasis in which mouse prostatic epithelial stem cells are concentrated in the proximal region of prostatic ducts while the transit-amplifying cells occupy the distal region of the ducts. This model can account for many biological differences between cells of the proximal and distal regions, and has implications for prostatic disease formation.
引用
收藏
页码:1257 / 1265
页数:9
相关论文
共 74 条
[1]   CIRCANNUAL CHANGES IN SERUM TESTOSTERONE CONCENTRATIONS OF ADULT AND YEARLING WOODCHUCKS (MARMOTA-MONAX) [J].
BALDWIN, BH ;
TENNANT, BC ;
REIMERS, TJ ;
COWAN, RG ;
CONCANNON, PW .
BIOLOGY OF REPRODUCTION, 1985, 32 (04) :804-812
[2]   Telomerase activity in normal adult brown Norway rat seminal vesicle: Regional distribution and age-dependent changes [J].
Banerjee, PP ;
Banerjee, S ;
Zirkin, BR ;
Brown, TR .
ENDOCRINOLOGY, 1998, 139 (03) :1075-1081
[3]   3 CLONAL TYPES OF KERATINOCYTE WITH DIFFERENT CAPACITIES FOR MULTIPLICATION [J].
BARRANDON, Y ;
GREEN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (08) :2302-2306
[4]   Expression of CD34 and Myf5 defines the majority of quiescent adult skeletal muscle satellite cells [J].
Beauchamp, JR ;
Heslop, L ;
Yu, DSW ;
Tajbakhsh, S ;
Kelly, RG ;
Wernig, A ;
Buckingham, ME ;
Partridge, TA ;
Zammit, PS .
JOURNAL OF CELL BIOLOGY, 2000, 151 (06) :1221-1233
[5]   FUNCTIONAL ISOLATION AND CHARACTERIZATION OF HUMAN HEMATOPOIETIC STEM-CELLS [J].
BERARDI, AC ;
WANG, AL ;
LEVINE, JD ;
LOPEZ, P ;
SCADDEN, DT .
SCIENCE, 1995, 267 (5194) :104-108
[6]  
Bonkhoff H, 1996, PROSTATE, V28, P98
[7]   MULTIDIRECTIONAL DIFFERENTIATION IN THE NORMAL, HYPERPLASTIC, AND NEOPLASTIC HUMAN PROSTATE - SIMULTANEOUS DEMONSTRATION OF CELL-SPECIFIC EPITHELIAL MARKERS [J].
BONKHOFF, H ;
STEIN, U ;
REMBERGER, K .
HUMAN PATHOLOGY, 1994, 25 (01) :42-46
[8]   THE PROLIFERATIVE FUNCTION OF BASAL CELLS IN THE NORMAL AND HYPERPLASTIC HUMAN PROSTATE [J].
BONKHOFF, H ;
STEIN, U ;
REMBERGER, K .
PROSTATE, 1994, 24 (03) :114-118
[9]  
BOSLAND MC, 1990, CANCER RES, V50, P691
[10]  
CASHMAN JD, 1990, BLOOD, V75, P96