Plasma cell survival is mediated by synergistic effects of cytokines and adhesion-dependent signals

被引:377
作者
Cassese, G
Arce, S
Hauser, AE
Lehnert, K
Moewes, B
Mostarac, M
Muehlinghaus, G
Szyska, M
Radbruch, A
Manz, RA
机构
[1] Deutsch Rheumaforschungszentrum, Dept Humoral Immunol, D-10117 Berlin, Germany
[2] Deutsch Rheumaforschungszentrum, Dept Cellular Immunol, D-10117 Berlin, Germany
关键词
D O I
10.4049/jimmunol.171.4.1684
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Recent results suggest that plasma cell longevity is not an intrinsic capacity, but depends on yet unknown factors produced in their environment. In this study, we show that the cytokines IL-5, IL-6, TNF-alpha, and stromal cell-derived factor-la as well as signaling via CD44 support the survival of isolated bone marrow plasma cells. The cytokines IL-7 and stem cell factor, crucially important for early B cell development, do not mediate plasma cell survival, indicating that plasma cells and early B cells have different survival requirements. As shown in IL-6-deficient mice, IL-6 is required for a normal induction, but not for the maintenance of plasma cell responses in vivo, indicating that the effects of individual survival factors are redundant. Optimal survival of isolated plasma cells requires stimulation by a combination of factors acting synergistically. These results strongly support the concept that plasma cell survival depends on niches in which a combination of specific signals, including IL-5, IL-6, stromal cell-derived factor-1alpha, TNF-alpha, and ligands for CD44, provides an environment required to mediate plasma cell longevity.
引用
收藏
页码:1684 / 1690
页数:7
相关论文
共 50 条
[11]
Chemotactic responsiveness toward ligands for CXCR3 and CXCR4 is regulated on plasma blasts during the time course of a memory immune response [J].
Hauser, AE ;
Debes, GF ;
Arce, S ;
Cassese, G ;
Hamann, A ;
Radbruch, A ;
Manz, RA .
JOURNAL OF IMMUNOLOGY, 2002, 169 (03) :1277-1282
[12]
CD44 - A MOLECULE INVOLVED IN LEUKOCYTE ADHERENCE AND T-CELL ACTIVATION [J].
HAYNES, BF ;
TELEN, MJ ;
HALE, LP ;
DENNING, SM .
IMMUNOLOGY TODAY, 1989, 10 (12) :423-428
[13]
DISTINCT SHORT-LIVED AND LONG-LIVED ANTIBODY-PRODUCING CELL-POPULATIONS [J].
HO, F ;
LORTAN, JE ;
MACLNNAN, ICM ;
KHAN, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1986, 16 (10) :1297-1301
[14]
Physiology - Chemokines beyond inflammation [J].
Horuk, R .
NATURE, 1998, 393 (6685) :524-525
[15]
JEME NK, 1974, TRANSPLANT REV, V18, P130
[16]
AUTOCRINE GENERATION AND REQUIREMENT OF BSF-2/IL-6 FOR HUMAN MULTIPLE MYELOMAS [J].
KAWANO, M ;
HIRANO, T ;
MATSUDA, T ;
TAGA, T ;
HORII, Y ;
IWATO, K ;
ASAOKU, H ;
TANG, B ;
TANABE, O ;
TANAKA, H ;
KURAMOTO, A ;
KISHIMOTO, T .
NATURE, 1988, 332 (6159) :83-85
[17]
Knödel M, 1999, EUR J IMMUNOL, V29, P2988
[18]
Kondo M, 2000, CURR TOP MICROBIOL, V251, P59
[19]
Interleukin 6 influences germinal center development and antibody production via a contribution of C3 complement component [J].
Kopf, M ;
Herren, S ;
Wiles, MV ;
Pepys, MB ;
Kosco-Vilbois, MH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (10) :1895-1906
[20]
CD44 AND ITS INTERACTION WITH EXTRACELLULAR-MATRIX [J].
LESLEY, J ;
HYMAN, R ;
KINCADE, PW .
ADVANCES IN IMMUNOLOGY, VOL 54, 1993, 54 :271-335