CFTR EXPRESSION IS REGULATED DURING BOTH THE CYCLE OF THE SEMINIFEROUS EPITHELIUM AND THE ESTROUS-CYCLE OF RODENTS

被引:124
作者
TREZISE, AEO
LINDER, CC
GRIEGER, D
THOMPSON, EW
MEUNIER, H
GRISWOLD, MD
BUCHWALD, M
机构
[1] HOSP SICK CHILDREN, RES INST, DEPT GENET, TORONTO M5G 1X8, ONTARIO, CANADA
[2] HOSP SICK CHILDREN, RES INST, DIV ENDOCRINOL, TORONTO M5G 1X8, ONTARIO, CANADA
[3] UNIV TORONTO, DEPT CLIN BIOCHEM, TORONTO M5G 1X8, ON, CANADA
[4] UNIV TORONTO, DEPT MOLEC & MED GENET, TORONTO M5G 1X8, ON, CANADA
[5] WASHINGTON STATE UNIV, BIOCHEM & BIOPHYS PROGRAM, PULLMAN, WA 99164 USA
[6] GEORGETOWN UNIV, MED CTR, VINCENT T LOMBARDI CANC RES CTR, WASHINGTON, DC 20007 USA
关键词
D O I
10.1038/ng0293-157
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Severely reduced, fertility is a common finding in cystic fibrosis (CF). We used in situ hybridization to examine the cell-specific expression of CFTR in the reproductive organs of rodents. In males CFTR mRNA is found in the round spermatids (spermatogenic stages V-X) and in the principal cells that line the initial segment of the epididymis. In both the testis and the epididymis, CFTR expression is developmentally regulated suggesting that the defect in the genital tract of male CF patients is of developmental origin. CFTR expression in the luminal and glandular epithelium of the uterus is regulated during the oestrous cycle and is maximal at pro-oestrus. Our results provide a biological rationale for the reduced fertility of CF patients, and suggest a possible cause for the comparatively poorer prognosis for women with CF.
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收藏
页码:157 / 164
页数:8
相关论文
共 49 条
[1]   GENERATION OF CAMP-ACTIVATED CHLORIDE CURRENTS BY EXPRESSION OF CFTR [J].
ANDERSON, MP ;
RICH, DP ;
GREGORY, RJ ;
SMITH, AE ;
WELSH, MJ .
SCIENCE, 1991, 251 (4994) :679-682
[2]   THE GENE ENCODING MULTIDRUG RESISTANCE IS INDUCED AND EXPRESSED AT HIGH-LEVELS DURING PREGNANCY IN THE SECRETORY EPITHELIUM OF THE UTERUS [J].
ARCECI, RJ ;
CROOP, JM ;
HORWITZ, SB ;
HOUSMAN, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (12) :4350-4354
[3]  
BADLEY JE, 1988, BIOTECHNIQUES, V6, P114
[4]   PURIFICATION AND FUNCTIONAL RECONSTITUTION OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) [J].
BEAR, CE ;
LI, CH ;
KARTNER, N ;
BRIDGES, RJ ;
JENSEN, TJ ;
RAMJEESINGH, M ;
RIORDAN, JR .
CELL, 1992, 68 (04) :809-818
[5]   GENETICALLY HAPLOID SPERMATIDS ARE PHENOTYPICALLY DIPLOID [J].
BRAUN, RE ;
BEHRINGER, RR ;
PESCHON, JJ ;
BRINSTER, RL ;
PALMITER, RD .
NATURE, 1989, 337 (6205) :373-376
[6]  
BRUGMAN SM, 1987, CYSTIC FIBROSIS, P323
[7]   PROTAMINE TRANSCRIPT SHARING AMONG POSTMEIOTIC SPERMATIDS [J].
CALDWELL, KA ;
HANDEL, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2407-2411
[8]   TRACHEOBRONCHIAL CYTOLOGIC CHANGES DURING MENSTRUAL CYCLE [J].
CHALON, J ;
LOEW, DAY ;
ORKIN, LR .
JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1971, 218 (13) :1928-&
[9]   DEFECTIVE INTRACELLULAR-TRANSPORT AND PROCESSING OF CFTR IS THE MOLECULAR-BASIS OF MOST CYSTIC-FIBROSIS [J].
CHENG, SH ;
GREGORY, RJ ;
MARSHALL, J ;
PAUL, S ;
SOUZA, DW ;
WHITE, GA ;
ORIORDAN, CR ;
SMITH, AE .
CELL, 1990, 63 (04) :827-834
[10]   DEFECTIVE EPITHELIAL CHLORIDE TRANSPORT IN A GENE-TARGETED MOUSE MODEL OF CYSTIC-FIBROSIS [J].
CLARKE, LL ;
GRUBB, BR ;
GABRIEL, SE ;
SMITHIES, O ;
KOLLER, BH ;
BOUCHER, RC .
SCIENCE, 1992, 257 (5073) :1125-1128