Differential regulation of splenic CD8- dendritic cells and marginal zone B cells by Notch ligands.

The importance of Notch signaling to maintain CD8- dendritic cells (DCs) in the spleen has recently been revealed. However, the ligand responsible for this Notch signaling has not been determined yet. In this study, we demonstrated that blocking of Delta-like (Dll) 1 alone had no significant effect on the maintenance of CD8- DCs while marginal zone (MZ) B cells were significantly reduced in the spleen of mice. On the other hand, blocking of Dll1, Dll4, Jagged1 and Jagged2 significantly decreased CD8- DCs. All these Notch ligands are expressed predominantly in the red pulp of the spleen where CD8- DCs reside. These results indicate a differential regulation of CD8- DCs and MZ B cells by Notch ligands in the spleen.

[1]  K. Okumura,et al.  Delta-like 1 is essential for the maintenance of marginal zone B cells in normal mice but not in autoimmune mice. , 2008, International immunology.

[2]  P. Kivisäkk,et al.  Jagged1 and Delta1 Differentially Regulate the Outcome of Experimental Autoimmune Encephalomyelitis1 , 2007, The Journal of Immunology.

[3]  B. Reizis,et al.  Notch–RBP-J signaling controls the homeostasis of CD8− dendritic cells in the spleen , 2007, The Journal of experimental medicine.

[4]  M. Nussenzweig,et al.  Origin of dendritic cells in peripheral lymphoid organs of mice , 2007, Nature Immunology.

[5]  D. Gabrilovich,et al.  Regulation of dendritic-cell differentiation by bone marrow stroma via different Notch ligands. , 2007, Blood.

[6]  R. Steinman,et al.  Differential Antigen Processing by Dendritic Cell Subsets in Vivo , 2007, Science.

[7]  S. Bray Notch signalling: a simple pathway becomes complex , 2006, Nature Reviews Molecular Cell Biology.

[8]  C. Guidos,et al.  Regulation of intrathymic T‐cell development by Lunatic Fringe– Notch1 interactions , 2006, Immunological reviews.

[9]  T. Banks,et al.  Intrinsic lymphotoxin-beta receptor requirement for homeostasis of lymphoid tissue dendritic cells. , 2005, Immunity.

[10]  S. Pillai,et al.  Marginal zone B cells. , 2005, Annual review of immunology.

[11]  N. Tamaoki,et al.  Delta-like 1 is necessary for the generation of marginal zone B cells but not T cells in vivo , 2004, Nature Immunology.

[12]  Freddy Radtke,et al.  Notch regulation of lymphocyte development and function , 2004, Nature Immunology.

[13]  U. Lendahl,et al.  Characterization of Notch3‐deficient mice: Normal embryonic development and absence of genetic interactions with a Notch1 mutation , 2003, Genesis.

[14]  R. Steinman Some interfaces of dendritic cell biology , 2003, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

[15]  S. Aizawa,et al.  Notch2 is preferentially expressed in mature B cells and indispensable for marginal zone B lineage development. , 2003, Immunity.

[16]  T. Honjo,et al.  Regulation of marginal zone B cell development by MINT, a suppressor of Notch/RBP-J signaling pathway. , 2003, Immunity.

[17]  T. Honjo,et al.  Notch–RBP-J signaling is involved in cell fate determination of marginal zone B cells , 2002, Nature Immunology.

[18]  Yong‐jun Liu,et al.  Mouse and human dendritic cell subtypes , 2002, Nature Reviews Immunology.

[19]  J. Cyster,et al.  Splenic T Zone Development Is B Cell Dependent , 2001, The Journal of experimental medicine.

[20]  S. Artavanis-Tsakonas,et al.  Notch Signaling : Cell Fate Control and Signal Integration in Development , 1999 .