Specific association of type I c-abl with ran GTPase in lipopolysaccharide-mediated differentiation

被引:6
作者
Daniel, R
Chung, SW
Eisenstein, TK
Sultzer, BM
Wong, PMC [1 ]
机构
[1] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Dept Pathol & Lab Med, Philadelphia, PA 19140 USA
[2] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Dept Microbiol & Immunol, Philadelphia, PA 19140 USA
[3] Stem Cell Therapeut, King Of Prussia, PA 19406 USA
关键词
Ran; LPS; endotoxin; sepsis; c-Abl isoform;
D O I
10.1038/sj.onc.1204361
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
Each of several isoforms of c-Abl may be involved in different biological functions. Type I c-Abl has been shown to be involved in LPS-induced differentiation and Type IV c-Abl, apoptosis, Ran has recently been shown to be involved in LPS endotoxin signal transduction, Here we show that Type I c-Abl associates with Ran. Formation of this complex is specific, as Ran did not associate with the highly homologous Type IV c-Abl isoform, In non-stimulated lymphoid B cells, Type I c-Abl tyrosine kinase is inactive, whereas Type IV kinase is active. Formation of Type I c-Abl/Ran complex and activation of Type I c-Abl kinase activity are LPS dose-dependent. This complex is detectable in B cells of endotoxin-sensitive inbred mice but absent in B cells of endotoxin-resistant mice. These findings therefore suggest that Type I c-Abl and Ran are important targets in lipopolysaccharide-induced biological responses of hematopoietic cells.
引用
收藏
页码:2618 / 2625
页数:8
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[31]   TRANSLATION OF 15-LIPOXYGENASE MESSENGER-RNA IS INHIBITED BY A PROTEIN THAT BINDS TO A REPEATED SEQUENCE IN THE 3' UNTRANSLATED REGION [J].
OSTARECKLEDERER, A ;
OSTARECK, DH ;
STANDART, N ;
THIELE, BJ .
EMBO JOURNAL, 1994, 13 (06) :1476-1481
[32]   ABL PROTEIN-TYROSINE KINASE SELECTS THE CRK ADAPTER AS A SUBSTRATE USING SH3-BINDING SITES [J].
REN, RB ;
YE, ZS ;
BALTIMORE, D .
GENES & DEVELOPMENT, 1994, 8 (07) :783-795
[33]   RNA binding and translational suppression by bicoid [J].
RiveraPomar, R ;
Niessing, D ;
SchmidtOtt, U ;
Gehring, WJ ;
Jackle, H .
NATURE, 1996, 379 (6567) :746-749
[34]   THE NUCLEAR TYROSINE KINASE C-ABL NEGATIVELY REGULATES CELL-GROWTH [J].
SAWYERS, CL ;
MCLAUGHLIN, J ;
GOGA, A ;
HAVLIK, M ;
WITTE, O .
CELL, 1994, 77 (01) :121-131
[35]   Interaction between ATM protein and c-Abl in response to DNA damage [J].
Shafman, T ;
Khanna, KK ;
Kedar, P ;
Spring, K ;
Kozlov, S ;
Yen, T ;
Hobson, K ;
Gatei, M ;
Zhang, N ;
Watters, D ;
Egerton, M ;
Shiloh, Y ;
Kharbanda, S ;
Kufe, D ;
Lavin, MF .
NATURE, 1997, 387 (6632) :520-523
[36]   A CONSERVED AU SEQUENCE FROM THE 3' UNTRANSLATED REGION OF GM-CSF MESSENGER-RNA MEDIATES SELECTIVE MESSENGER-RNA DEGRADATION [J].
SHAW, G ;
KAMEN, R .
CELL, 1986, 46 (05) :659-667
[37]   GENETIC-CONTROL OF HOST RESPONSES TO ENDOTOXIN [J].
SULTZER, BM .
INFECTION AND IMMUNITY, 1972, 5 (01) :107-&
[38]   Nuclear-cytoplasmic shuttling of C-ABL tyrosine kinase [J].
Taagepera, S ;
McDonald, D ;
Loeb, JE ;
Whitaker, LL ;
McElroy, AK ;
Wang, JYJ ;
Hope, TJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (13) :7457-7462
[39]   Cycling, stressed-out and nervous: cellular functions of c-Abl [J].
Van Etten, RA .
TRENDS IN CELL BIOLOGY, 1999, 9 (05) :179-186
[40]   ABL TYROSINE KINASE IN SIGNAL-TRANSDUCTION AND CELL-CYCLE REGULATION [J].
WANG, JYJ .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1993, 3 (01) :35-43