Novel B219/OB receptor isoforms: Possible role of leptin in hematopoiesis and reproduction

被引:595
作者
Cioffi, JA
Shafer, AW
Zupancic, TJ
SmithGbur, J
Mikhail, A
Platika, D
Snodgrass, HR
机构
[1] PROGENITOR INC,COLUMBUS,OH 43212
[2] OHIO STATE UNIV,SCH MED,DIV BONE MARROW TRANSPLANTAT,DEPT INTERNAL MED,COLUMBUS,OH 43210
关键词
D O I
10.1038/nm0596-585
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hematopoietic development is a complex process that involves a large number of growth factors and cytokines. Many cytokines are known to act on more mature, lineage-restricted cells of the hematopoietic system(1,2). However, no specific factors have yet been identified that induce the expansion of the most primitive hematopoietic cells without also inducing differentiation. To search for such factors, we isolated novel cell lines from the yolk sac in order to identify genes important in early hematopoietic and endothelial development. This approach led to the discovery of B219, a sequence that is expressed in at least four isoforms in very primitive hematopoietic cell populations and which may represent a novel hemopoietin receptor. The recently published receptor(3) for the obesity (ob) gene product (leptin)(4) is an isoform of B219 with a nearly identical ligand binding domain. B279/obr is expressed in the yolk sac, early fetal liver, enriched hematopoietic stem cells and in a variety of lymphohematopoietic cell lines. B279/obr is also expressed at high levels in adult reproductive organs. B279/obr maps to human chromosome 1p32, a region syntenic with the recently reported location of obr on murine chromosome 4 (ref. 5).
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页码:585 / 589
页数:5
相关论文
共 29 条
[1]   CYTOKINES - COORDINATORS OF IMMUNE AND INFLAMMATORY RESPONSES [J].
ARAI, K ;
LEE, F ;
MIYAJIMA, A ;
MIYATAKE, S ;
ARAI, N ;
YOKOTA, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :783-836
[2]   MOLECULAR MAPPING OF THE MOUSE DB MUTATION [J].
BAHARY, N ;
LEIBEL, RL ;
JOSEPH, L ;
FRIEDMAN, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (21) :8642-8646
[3]  
BARRACLOUGH CA, HDB PHYSL 7 1, P29
[5]  
BJORNTORP P, 1993, ANN NY ACAD SCI, V676, P242
[6]   HYPOTHALAMIC AND GENETIC OBESITY IN EXPERIMENTAL-ANIMALS - AUTONOMIC AND ENDOCRINE HYPOTHESIS [J].
BRAY, GA ;
YORK, DA .
PHYSIOLOGICAL REVIEWS, 1979, 59 (03) :719-809
[7]   EXPRESSION OF FC-GAMMA-RIII DEFINES DISTINCT SUBPOPULATIONS OF FETAL LIVER B-CELL AND MYELOID PRECURSORS [J].
CARLSSON, L ;
CANDEIAS, S ;
STAERZ, U ;
KELLER, G .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (08) :2308-2317
[8]   Correction of the sterility defect in homozygous obese female mice by treatment with the human recombinant leptin [J].
Chehab, FE ;
Lim, ME ;
Lu, RH .
NATURE GENETICS, 1996, 12 (03) :318-320
[9]   Evidence that the diabetes gene encodes the leptin receptor: Identification of a mutation in the leptin receptor gene in db/db mice [J].
Chen, H ;
Charlat, O ;
Tartaglia, LA ;
Woolf, EA ;
Weng, X ;
Ellis, SJ ;
Lakey, ND ;
Culpepper, J ;
Moore, KJ ;
Breitbart, RE ;
Duyk, GM ;
Tepper, RI ;
Morgenstern, JP .
CELL, 1996, 84 (03) :491-495
[10]  
Civin C I, 1993, J Hematother, V2, P137, DOI 10.1089/scd.1.1993.2.137