Increased apoptosis of bone marrow pre-B cells in old mice associated with their low number

被引:45
作者
Kirman, I
Zhao, KS
Wang, YF
Szabo, P
Telford, W
Weksler, ME [1 ]
机构
[1] Cornell Univ, Coll Med, Div Geriatr & Gerontol, New York, NY 10021 USA
[2] Hosp Special Surg, New York, NY 10021 USA
关键词
apoptosis; B cells; BCL-X-L; IL-7;
D O I
10.1093/intimm/10.9.1385
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The number of bone marrow pre-a cells is significantly lower in 18- than in 2-month-old BALB/c mice. The percentage of apoptotic pre-a cells, freshly isolated or cultured, from 18-month-old mice was significantly greater than from P-month-old mice. The increased percentage of apoptotic pre-a cells from old mice was associated with a decreased level of bcl-x(L) mRNA, detected by RT-PCR, and of Bcl-x(L) protein, detected by intracellular staining. Consistent with an age-associated increase in apoptosis in pre-a cells was the fact that significantly fewer pre-a cells were generated after in vitro cultures of pro-a cells from old as compared to young mice, Furthermore, fewer pre-a cells survived and fewer sig-expressing a cells were generated in cultures of pre-a cells from old as compared to young mice. In addition, there was no detectable difference in the secretion of IL-7 by bone marrow cells from 2- or 18-month-old mice. Thus, increased apoptosis of bone marrow pre-a cells in old mice appears to contribute to their decreased number.
引用
收藏
页码:1385 / 1392
页数:8
相关论文
共 30 条
[1]  
ARMITAGE RJ, 1992, BLOOD, V79, P1738
[2]  
DITTEL BN, 1995, J IMMUNOL, V154, P58
[3]   HOW B-PRECURSOR CELLS ARE DRIVEN TO CYCLE [J].
ERA, T ;
NISHIKAWA, S ;
SUDO, T ;
WANG, FH ;
OGAWA, M ;
KUNISADA, T ;
HAYASHI, SI ;
NISHIKAWA, SI .
IMMUNOLOGICAL REVIEWS, 1994, 137 :35-51
[4]   Frequent aberrant immunoglobulin gene rearrangements in pro-B cells revealed by a bcl-x(L) transgene [J].
Fang, W ;
Mueller, DL ;
Pennell, CA ;
Rivard, JJ ;
Li, YS ;
Hardy, RR ;
Schlissel, MS ;
Behrens, TW .
IMMUNITY, 1996, 4 (03) :291-299
[5]   DISTINCTIVE GROWTH REQUIREMENTS AND GENE-EXPRESSION PATTERNS DISTINGUISH PROGENITOR B-CELLS FROM PRE-B-CELLS [J].
FAUST, EA ;
SAFFRAN, DC ;
TOKSOZ, D ;
WILLIAMS, DA ;
WITTE, ON .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (04) :915-923
[6]   CLONING OF THE HUMAN AND MURINE INTERLEUKIN-7 RECEPTORS - DEMONSTRATION OF A SOLUBLE FORM AND HOMOLOGY TO A NEW RECEPTOR SUPERFAMILY [J].
GOODWIN, RG ;
FRIEND, D ;
ZIEGLER, SF ;
JERZY, R ;
FALK, BA ;
GIMPEL, S ;
COSMAN, D ;
DOWER, SK ;
MARCH, CJ ;
NAMEN, AE ;
PARK, LS .
CELL, 1990, 60 (06) :941-951
[7]   RESOLUTION AND CHARACTERIZATION OF PRO-B AND PRE-PRO-B CELL STAGES IN NORMAL MOUSE BONE-MARROW [J].
HARDY, RR ;
CARMACK, CE ;
SHINTON, SA ;
KEMP, JD ;
HAYAKAWA, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (05) :1213-1225
[8]   STEPWISE PROGRESSION OF B-LINEAGE DIFFERENTIATION SUPPORTED BY INTERLEUKIN-7 AND OTHER STROMAL CELL MOLECULES [J].
HAYASHI, SI ;
KUNISADA, T ;
OGAWA, M ;
SUDO, T ;
KODAMA, H ;
SUDA, T ;
NISHIKAWA, S ;
NISHIKAWA, SI .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (05) :1683-1695
[9]   INTERLEUKIN-7 RESPONSIVENESS OF B220+ B-CELL PRECURSORS FROM BONE-MARROW DECREASES IN AGING MICE [J].
JONSSON, JI ;
PHILLIPS, RA .
CELLULAR IMMUNOLOGY, 1993, 147 (02) :267-278
[10]   CARDIORESPIRATORY EFFECTS OF IMMUNOTHERAPY WITH INTERLEUKIN-2 [J].
LEE, RE ;
LOTZE, MT ;
SKIBBER, JM ;
TUCKER, E ;
BONOW, RO ;
OGNIBENE, FP ;
CARRASQUILLO, JA ;
SHELHAMER, JH ;
PARRILLO, JE ;
ROSENBERG, SA .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (01) :7-20