CDK inhibitor p18INK4c is required for the generation of functional plasma cells

被引:87
作者
Tourigny, MR
Ursini-Siegel, J
Lee, H
Toellner, KM
Cunningham, AF
Franklin, DS
Ely, S
Chen, MH
Qin, XF
Xiong, Y
MacLennan, ICM
Chen-Kiang, S
机构
[1] Cornell Univ, Weill Med Coll, Dept Pathol, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Dept Microbiol & Immunol, New York, NY 10021 USA
[3] Univ Birmingham, Sch Med, Birmingham, W Midlands, England
[4] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[5] Rockefeller Univ, Lab Mol Immunol, New York, NY 10021 USA
[6] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
关键词
D O I
10.1016/S1074-7613(02)00364-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B cell terminal differentiation is associated with the onset of high-level antibody secretion and cell cycle arrest. Here the cyclin-dependent kinase (CDK) inhibitor p18(INK4c) is shown to be required within B cells for both terminating cell proliferation and differentiation of functional plasma cells. In its absence, B cells hyperproliferate in germinal centers and extrafollicular foci in response to T-dependent antigens but serum antibody titers are severely reduced, despite unimpaired germinal center formation, class switch recombination, variable region-directed hypermutation, and differentiation to antibody-containing plasmacytoid cells. The novel link between cell cycle control and plasma cell differentiation may, at least in part, relate to p18(INK4c) inhibition of CDK6. Cell cycle arrest mediated by p18(INK4c) is therefore requisite for the generation of functional plasma cells.
引用
收藏
页码:179 / 189
页数:11
相关论文
共 42 条
  • [1] Immunological memory and protective immunity: Understanding their relation
    Ahmed, R
    Gray, D
    [J]. SCIENCE, 1996, 272 (5258) : 54 - 60
  • [2] IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA
    Calfon, M
    Zeng, HQ
    Urano, F
    Till, JH
    Hubbard, SR
    Harding, HP
    Clark, SG
    Ron, D
    [J]. NATURE, 2002, 415 (6867) : 92 - 96
  • [3] CHAN FKM, 1995, MOL CELL BIOL, V15, P2682
  • [4] BLIMP-I: trigger for differentiation of myeloid lineage
    Chang, DH
    Angelin-Duclos, C
    Calame, K
    [J]. NATURE IMMUNOLOGY, 2000, 1 (02) : 169 - 176
  • [5] STRUCTURE OF PRIMARY ANTI-(4-HYDROXY-3-NITROPHENYL)ACETYL (NP) ANTIBODIES IN NORMAL AND IDIOTYPICALLY SUPPRESSED C57BL/6 MICE
    CUMANO, A
    RAJEWSKY, K
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1985, 15 (05) : 512 - 520
  • [6] Attenuation of apoptosis underlies B lymphocyte stimulator enhancement of humoral immune response
    Do, RKG
    Hatada, E
    Lee, H
    Tourigny, MR
    Hilbert, D
    Chen-Kiang, S
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (07) : 953 - 964
  • [7] Induction of p18(INK4c) and its predominant association with CDK4 and CDK6 during myogenic differentiation
    Franklin, DS
    Xiong, Y
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (10) : 1587 - 1599
  • [8] CDK inhibitors p18INK4c and p27Kip1 mediate two separate pathways to collaboratively suppress pituitary tumorigenesis
    Franklin, DS
    Godfrey, VL
    Lee, HY
    Kovalev, GI
    Schoonhoven, R
    Chen-Kiang, S
    Su, LS
    Xiong, Y
    [J]. GENES & DEVELOPMENT, 1998, 12 (18) : 2899 - 2911
  • [9] Isolation and characterization of p19(INK4d), a p16-related inhibitor specific to CDK6 and CDK4
    Guan, KL
    Jenkins, CW
    Li, Y
    OKeefe, CL
    Noh, S
    Wu, XY
    Zariwala, M
    Matera, AG
    Xiong, Y
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (01) : 57 - 70
  • [10] GROWTH SUPPRESSION BY P18, A P16(INK4/MTS1)-RELATED AND P14(INK4B/MTS2)-RELATED CDK6 INHIBITOR, CORRELATES WITH WILD-TYPE PRB FUNCTION
    GUAN, KL
    JENKINS, CW
    LI, Y
    NICHOLS, MA
    WU, XY
    OKEEFE, CL
    MATERA, AG
    XIONG, Y
    [J]. GENES & DEVELOPMENT, 1994, 8 (24) : 2939 - 2952