CD38 low IgG-secreting cells are precursors of various CD38 high-expressing plasma cell populations

被引:66
作者
Arce, S
Luger, E
Muehlinghaus, G
Cassese, G
Hauser, A
Horst, A
Lehnert, K
Odendahl, M
Hönemann, D
Heller, KD
Kleinschmidt, H
Berek, C
Dörner, T
Krenn, V
Hiepe, F
Bargou, R
Radbruch, A
Manz, RA
机构
[1] Deutsches Rheuma Forschungszentrum, D-10117 Berlin, Germany
[2] Miltenyi Biotec GmbH, Bergisch Gladbach, Germany
[3] Humboldt Univ, Berlin, Germany
[4] Orthopad Klin, Braunschweig, Germany
关键词
antibodies; B lymphocytes; cellular differentiation; memory;
D O I
10.1189/jlb.0603279
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Despite the important role immunoglobulin G (IgG)-secreting plasma cells play in memory immune responses, the differentiation and homeostasis of these cells are not completely understood. Here, we studied the differentiation of human IgG-secreting cells ex vivo and in vitro, identifying these cells by the cellular affinity matrix technology. Several subpopulations of IgG-secreting cells were identified among the cells isolated from tonsils and bone marrow, particularly differing in the expression levels of CD9, CD19, and CD38. CD38 low IgG-secreting cells were present exclusively in the tonsils. A major fraction of these cells appeared to be early plasma cell precursors, as upon activation of B cells in vitro, IgG secretion preceded up-regulation of CD38, and on tonsillar sections, IgG-containing, CD38 low cells with a plasmacytoid phenotype were found in follicles, where plasma cell differentiation starts. A unitary phenotype of migratory peripheral blood IgG-secreting cells suggests that all bone marrow plasma cell populations share a common precursor cell. These data are compatible with a multistep model for plasma cell differentiation and imply that a common CD38 low IgG-secreting precursor gives rise to a diverse plasma cell compartment.
引用
收藏
页码:1022 / 1028
页数:7
相关论文
共 41 条
[31]   The heterogeneity shown by human plasma cells from tonsil, blood, and bone marrow reveals graded stages of increasing maturity, but local profiles of adhesion molecule expression [J].
Medina, F ;
Segundo, C ;
Campos-Caro, A ;
González-García, I ;
Brieva, JA .
BLOOD, 2002, 99 (06) :2154-2161
[32]   Bcl-2(+) tonsillar plasma cells are rescued from apoptosis by bone marrow fibroblasts [J].
Merville, P ;
Dechanet, J ;
Desmouliere, A ;
Durand, I ;
deBouteiller, O ;
Garrone, P ;
Banchereau, J ;
Liu, YJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) :227-236
[33]   Disturbed peripheral B lymphocyte homeostasis in systemic lupus erythematosus [J].
Odendahl, M ;
Jacobi, A ;
Hansen, A ;
Feist, E ;
Hiepe, F ;
Burmester, GR ;
Lipsky, PE ;
Radbruch, A ;
Dörner, T .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5970-5979
[34]   Humoral immunity due to long-lived plasma cells [J].
Slifka, MK ;
Antia, R ;
Whitmire, JK ;
Ahmed, R .
IMMUNITY, 1998, 8 (03) :363-372
[35]   TOWARDS A COMPREHENSIVE VIEW OF IMMUNOGLOBULIN CLASS SWITCHING [J].
SNAPPER, CM ;
MOND, JJ .
IMMUNOLOGY TODAY, 1993, 14 (01) :15-17
[36]   Intrinsic constraint on plasmablast growth and extrinsic limits of plasma cell survival [J].
Sze, DMY ;
Toellner, KM ;
de Vinuesa, CG ;
Taylor, DR ;
MacLennan, ICM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (06) :813-821
[37]   A division-linked mechanism for the rapid generation of Ig-secreting cells from human memory B cells [J].
Tangye, SG ;
Avery, DT ;
Hodgkin, PD .
JOURNAL OF IMMUNOLOGY, 2003, 170 (01) :261-269
[38]  
TERSTAPPEN LWMM, 1990, BLOOD, V76, P1739
[39]  
VOLKMAN DJ, 1982, J IMMUNOL, V129, P107
[40]   The role of bone marrow-derived stromal cells in the maintenance of plasma cell longevity [J].
Wols, HAM ;
Underhill, GH ;
Kansas, GS ;
Witte, PL .
JOURNAL OF IMMUNOLOGY, 2002, 169 (08) :4213-4221