Initiation of plasma-cell differentiation is independent of the transcription factor Blimp-1

被引:206
作者
Kallies, Axel
Hasbold, Jhagvaral
Fairfax, Kirsten
Pridans, Clare
Emslie, Dianne
McKenzie, Brent S.
Lew, Andrew M.
Corcoran, Lynn M.
Hodgkin, Philip D.
Tarlinton, David M.
Nutt, Stephen L.
机构
[1] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[2] Univ Melbourne, Dept Expt Med, Parkville, Vic 3052, Australia
[3] Univ WEstern Sydney, Richmond, NW 2753, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.immuni.2007.04.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Blimp-1 is considered an essential regulator of the terminal differentiation of B cells into antibody-secreting plasma cells. We show here that Rag1(-/-) mice reconstituted with fetal liver cells homozygous for a DNA-binding-deficient mutant of Prdm1 (the gene encoding Blimp-1) lack a defined plasma-cell compartment, yet show detectable amounts of all immunoglobulin isotypes. In vitro analysis revealed that Blimp-1 is not required for the initiation of antibody secretion but is essential for subsequent high immunoglobulin production. Blimp-1-independent differentiation was blocked at a pre-plasmablast stage characterized by decreased Pax5 expression and the activation of plasma-cell genes. Analysis of Blimp-1-sufficient differentiation revealed a phase prior to Blimp-1 expression in which several genes normally repressed by Pax5 are re-expressed, suggesting that plasma-cell differentiation is initiated by the inhibition of Pax5 function. Our results indicate that full plasma-cell differentiation but not commitment to the plasma-cell fate requires the expression of functional Blimp-1.
引用
收藏
页码:555 / 566
页数:12
相关论文
共 43 条
[1]   Transfer of small resting B cells into immunodeficient hosts results in the selection of a self-renewing activated B cell population [J].
Agenès, F ;
Freitas, AA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (02) :319-329
[2]   Commitment of B lymphocytes to a plasma cell fate is associated with Blimp-1 expression in vivo [J].
Angelin-Duclos, C ;
Cattoretti, G ;
Lin, KI ;
Calame, K .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5462-5471
[3]   Early appearance of germinal center-derived memory B cells and plasma cells in blood after primary immunization [J].
Blink, EJ ;
Light, A ;
Kallies, A ;
Nutt, SL ;
Hodgkin, PD ;
Tarlinton, DM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (04) :545-554
[4]   Differential requirement for OBF-1 during antibody-secreting cell differentiation [J].
Corcoran, LM ;
Hasbold, J ;
Dietrich, W ;
Hawkins, E ;
Kallies, A ;
Nutt, SL ;
Tarlinton, DM ;
Matthias, P ;
Hodgkin, PD .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (09) :1385-1396
[5]   Gene repression by Pax5 in B cells is essential for blood cell homeostasis and is reversed in plasma cells [J].
Delogu, A ;
Schebesta, A ;
Sun, Q ;
Aschenbrenner, K ;
Perlot, T ;
Busslinger, M .
IMMUNITY, 2006, 24 (03) :269-281
[6]   Different kinetics of Blimp-1 induction in B cell subsets revealed by reporter gene [J].
Fairfax, Kirsten A. ;
Corcoran, Lynn M. ;
Pridans, Clare ;
Huntington, Nicholas D. ;
Kallies, Axel ;
Nutt, Stephen L. ;
Tarlinton, David M. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (07) :4104-4111
[7]   The balance between Pax5 and Id2 activities is the key to AID gene expression [J].
Gonda, H ;
Sugai, M ;
Nambu, Y ;
Katakai, T ;
Agata, Y ;
Mori, KJ ;
Yokota, Y ;
Shimizu, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (09) :1427-1437
[8]   Evidence from the generation of immunoglobulin G-secreting cells that stochastic mechanisms regulate lymphocyte differentiation [J].
Hasbold, J ;
Corcoran, LM ;
Tarlinton, DM ;
Tangye, SG ;
Hodgkin, PD .
NATURE IMMUNOLOGY, 2004, 5 (01) :55-63
[9]   Repression of Flt3 by Pax5 is crucial for B-cell lineage commitment [J].
Holmes, ML ;
Carotta, S ;
Corcoran, LM ;
Nutt, SL .
GENES & DEVELOPMENT, 2006, 20 (08) :933-938
[10]   Plasma cell differentiation and the unfolded protein response intersect at the transcription factor XBP-1 [J].
Iwakoshi, NN ;
Lee, AH ;
Vallabhajosyula, P ;
Otipoby, KL ;
Rajewsky, K ;
Glimcher, LH .
NATURE IMMUNOLOGY, 2003, 4 (04) :321-329