Negative selection at the pre-BCR checkpoint elicited by human μ heavy chains with unusual CDR3 regions

被引:42
作者
Minegishi, Y
Conley, ME
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[2] Univ Tennessee, Coll Med, Dept Pediat, Memphis, TN 38105 USA
关键词
D O I
10.1016/S1074-7613(01)00131-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Approximately 9% of in-frame mu heavy chain transcripts found in normal human pro-B cells encode proteins that can be expressed on the cell surface in the absence of surrogate or conventional light chains. These unusual mu heavy chains demonstrate preferential use of certain VH genes (VH3-23), frequent expression of DH regions in underrepresented reading frames, and an increased number of positively charged amino acids within the CDR3 region. Transcripts for these proteins are not found in pre-B cells or in mature B cells. When expressed in Jurkat T cells with the Ig alpha /Ig beta signal transduction module, these aberrant mu heavy chains induce cell activation and apoptosis. These results suggest that some mu heavy chains elicit negative selection at the pro-B cell to pre-B cell transition.
引用
收藏
页码:631 / 641
页数:11
相关论文
共 59 条
[1]  
ALZARI PM, 1988, ANNU REV IMMUNOL, V6, P555
[2]   A DNA INSERTION DELETION NECESSITATES AN ABERRANT RNA SPLICE ACCOUNTING FOR A MU-HEAVY CHAIN DISEASE PROTEIN [J].
BAKHSHI, A ;
GUGLIELMI, P ;
SIEBENLIST, U ;
RAVETCH, JV ;
JENSEN, JP ;
KORSMEYER, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2689-2693
[3]   RESTRICTED USE OF FETAL VH3 IMMUNOGLOBULIN GENES BY UNSELECTED B-CELLS IN THE ADULT - PREDOMINANCE OF 56P1-LIKE VH GENES IN COMMON VARIABLE IMMUNODEFICIENCY [J].
BRAUN, J ;
BERBERIAN, L ;
KING, L ;
SANZ, I ;
GOVAN, HL .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (05) :1395-1402
[4]   Analysis of the human V-H gene repertoire - Differential effects of selection and somatic hypermutation on human peripheral CD5(+)/IgM(+) and CD5(-)/IgM(+) B cells [J].
Brezinschek, HP ;
Foster, SJ ;
Brezinschek, RI ;
Dorner, T ;
DomiatiSaad, R ;
Lipsky, PE .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (10) :2488-2501
[5]   Immunoglobulin heavy chain gene replacement: A mechanism of receptor editing [J].
Chen, C ;
Nagy, Z ;
Prak, EL ;
Weigert, M .
IMMUNITY, 1995, 3 (06) :747-755
[6]   THE SITE AND STAGE OF ANTI-DNA B-CELL DELETION [J].
CHEN, C ;
NAGY, Z ;
RADIC, MZ ;
HARDY, RR ;
HUSZAR, D ;
CAMPER, SA ;
WEIGERT, M .
NATURE, 1995, 373 (6511) :252-255
[7]   Mutations in Btk in patients with presumed X-linked agammaglobulinemia [J].
Conley, ME ;
Mathias, D ;
Treadaway, J ;
Minegishi, Y ;
Rohrer, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1034-1043
[8]   Sequence of the human immunoglobulin diversity (D) segment locus: A systematic analysis provides no evidence for the use of DIR segments, inverted D segments, ''minor'' D segments or D-D recombination [J].
Corbett, SJ ;
Tomlinson, IM ;
Sonnhammer, ELL ;
Buck, D ;
Winter, G .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 270 (04) :587-597
[9]   FUNCTIONAL RECONSTITUTION OF AN IMMUNOGLOBULIN ANTIGEN RECEPTOR IN T-CELLS [J].
COSTA, TE ;
FRANKE, RR ;
SANCHEZ, M ;
MISULOVIN, Z ;
NUSSENZWEIG, MC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (06) :1669-1676
[10]   ANTIBODY-ANTIGEN COMPLEXES [J].
DAVIES, DR ;
PADLAN, EA ;
SHERIFF, S .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :439-473