EXPRESSION OF GROWTH-RELATED GENES IN HUMAN FETAL KIDNEY

被引:21
作者
GOODYER, PR
MULLIGAN, L
GOODYER, CG
机构
[1] MCGILL UNIV,MONTREAL CHILDRENS HOSP RES INST,DIV PEDIAT NEPHROL,MONTREAL H3A 2T5,QUEBEC,CANADA
[2] MCGILL UNIV,MONTREAL CHILDRENS HOSP RES INST,DEPT PEDIAT ENDOCRINOL,MONTREAL H3A 2T5,QUEBEC,CANADA
[3] ROYAL VICTORIA HOSP,LUDWIG INST CANC RES,MONTREAL H3A 1A1,QUEBEC,CANADA
关键词
FETAL KIDNEY; GROWTH FACTOR; TRANSFORMING GROWTH FACTOR-ALPHA; EPIDERMAL GROWTH FACTOR; AMNIOTIC FLUID;
D O I
10.1016/S0272-6386(12)80331-3
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
By the end of gestation, nephron formation in the human kidney is complete. Following local induction of metanephric mesenchyma, committed cells of each primitive renal vesicle must undergo a phase of rapid cell division. In order to identify genes which might regulate these events, we examined the expression profile of 22 proto-oncogenes in fetal versus adult human kidney. Among those expressed at especially high levels in the fetal tissue was the gene for epidermal growth factor receptor (EGFR). We were able to detect mRNA (by polymerase chain reaction [PCR] amplification) and peptide (by specific radioimmunoassay) for transforming growth factor-α (TGF-α) in fetal kidney, whereas epidermal growth factor (EGF) peptide was undetectable in midgestation kidney and amniotic fluid. TGF-α/EGFR interactions may direct renal cell proliferation in fetal life. © 1991, National Kidney Foundation, Inc.. All rights reserved.
引用
收藏
页码:608 / 610
页数:3
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