Consequences of exclusive expression in vivo of kit-ligand lacking the major proteolytic cleavage site

被引:73
作者
Tajima, Y
Moore, MAS
Soares, V
Ono, M
Kissel, H
Besmer, P
机构
[1] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Cell Biol Program, New York, NY 10021 USA
[3] Cornell Univ, Grad Sch Med Sci, Sloan Kettering Div, New York, NY 10021 USA
关键词
D O I
10.1073/pnas.95.20.11903
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Membrane growth factors that are processed to produce soluble ligands may function both as soluble factors and as membrane factors. The membrane growth factor Kit-ligand (KL), the ligand of the Kit receptor tyrosine kinase, is encoded at the SI locus, and mice carrying SI mutations have defects in hematopoiesis, gametogenesis, and melanogenesis. Two alternatively spliced KL transcripts encode two cell-associated KL protein products, KL-1 and KL-2, The KL-2 protein lacks the major proteolytic cleavage site for the generation of soluble KL, thus representing a more stable cell-associated form of KL, We investigated the consequences of exclusive expression of KL-2 in vivo, The KL gene in embryonic stem cells was modified and KL exon 6 was replaced with a PGKneoNTRtkpA cassette by homologous recombination, and mice carrying the Sl(KL2) allele were obtained. Sl(KL2)/Sl(KL2) mice had only slightly reduced levels of soluble KL in their serum, suggesting that in vivo KL-2 may be processed to produce soluble KL-2S, The steady-state characteristics of the hematopoietic system and progenitor numbers were normal, and the mutant animals were not anemic. However, mast cell numbers in the skin and peritoneum were reduced and the mutant animals displayed increased sensitivity to sublethal doses of gamma-irradiation. Therefore, KL-2 may substitute for KL-1 in most situations with the exception of the production of mast cells, and induced proteolytic cleavage of KL-1 to produce soluble KL may have a role in the regeneration of hematopoietic tissue after radiation injury.
引用
收藏
页码:11903 / 11908
页数:6
相关论文
共 35 条
[1]   Role of the juxtamembrane domains of the transforming growth factor-alpha precursor and the beta-amyloid precursor protein in regulated ectodomain shedding [J].
Arribas, J ;
LopezCasillas, F ;
Massague, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (27) :17160-17165
[2]  
BERNSTEIN SE, 1962, SCIENCE, V127, P428
[3]  
BESMER P, 1997, COLONY STIMULATING F, P369
[4]   The kit ligand encoded at the murine Steel locus: a pleiotropic growth and differentiation factor [J].
Besmer, Peter .
CURRENT OPINION IN CELL BIOLOGY, 1991, 3 (06) :939-946
[5]  
BOSENBERG MW, 1993, CURR OPIN CELL BIOL, V5, P823
[6]   STEEL-DICKIE MUTATION ENCODES A C-KIT LIGAND LACKING TRANSMEMBRANE AND CYTOPLASMIC DOMAINS [J].
BRANNAN, CI ;
LYMAN, SD ;
WILLIAMS, DE ;
EISENMAN, J ;
ANDERSON, DM ;
COSMAN, D ;
BEDELL, MA ;
JENKINS, NA ;
COPELAND, NG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :4671-4674
[7]   DEVELOPMENTAL ABNORMALITIES IN STEEL(17H) MICE RESULT FROM A SPLICING DEFECT IN THE STEEL FACTOR CYTOPLASMIC TAIL [J].
BRANNAN, CI ;
BEDELL, MA ;
RESNICK, JL ;
EPPIG, JJ ;
HANDEL, MA ;
WILLIAMS, DE ;
LYMAN, SD ;
DONOVAN, PJ ;
JENKINS, NA ;
COPELAND, NG .
GENES & DEVELOPMENT, 1992, 6 (10) :1832-1842
[8]   INVITRO DUPLICATION AND CURE OF HEMATOPOIETIC DEFECTS IN GENETICALLY ANEMIC MICE [J].
DEXTER, TM ;
MOORE, MAS .
NATURE, 1977, 269 (5627) :412-414
[9]   TRANSMEMBRANE FORM OF THE KIT LIGAND GROWTH-FACTOR IS DETERMINED BY ALTERNATIVE SPLICING AND IS MISSING IN THE SI(D) MUTANT [J].
FLANAGAN, JG ;
CHAN, DC ;
LEDER, P .
CELL, 1991, 64 (05) :1025-1035
[10]   RESPONSE OF W/WV AND SL/SLD ANEMIC MICE TO HEMOPOIETIC STIMULI [J].
HARRISON, DE ;
RUSSELL, ES .
BRITISH JOURNAL OF HAEMATOLOGY, 1972, 22 (02) :155-&