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Analysis of the maturation process of dendritic cells deficient for TNF and lymphotoxin-alpha reveals an essential role for TNF

Citation

Ritter, U and Meissner, A and Ott, J and Korner, H, Analysis of the maturation process of dendritic cells deficient for TNF and lymphotoxin-alpha reveals an essential role for TNF, Journal of Leukocyte Biology, 74, (2) pp. 216-222. ISSN 0741-5400 (2003) [Refereed Article]


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Copyright Statement

Copyright 2003 by Society for Leukocyte Biology

DOI: doi:10.1189/jlb.1202587

Abstract

Dendritic cells (DCs) generated from bone marrow (BM) precursor cells of C57BL/6 (B6.WT) mice and cultured in the presence of granulocyte macrophage-colony stimulating factor differentiate to mature BM-DCs spontaneously. These mature DCs are characterized by high levels of major histocompatibility complex (MHC) class II, CD40, and CD86 on their surface. To analyze the involvement of tumor necrosis factor (TNF) and the related cytokine lymphotoxin (LT)α in DC maturation, we studied the development of DCs from the BM of B6.TNF-/-, B6.LTα-/-, and B6.TNF/LTα-/- mice and compared it to B6.WT mice. Although the development of BM precursor cells to the level of immature DCs (CD11c +, MHC class IIlow, CD40low, and CD86 low) was equivalent in all genotypes, B6.TNF-/- and B6.TNF/LTα-/- cells showed an impaired capacity to differentiate to mature DCs. In contrast, mature BM-DCs generated from LTα-negative, immature DCs developed like B6.WT cells. Further studies revealed that once matured, the phenotype of all tested gynotypes was comparable. They expressed high levels of CD40 and CD86, were exclusively positive for the chemokine receptor (CCR)7 but negative for CCR5 and CCR2, and were able to enter the paracortex of draining lymph nodes. The limited maturation of TNF-deficient BM-DCs could be restored by mixing TNF-negative with TNF-positive Ly5.1 BM cells, and maturation of B6.WT DCs could be blocked with an anti-TNF monoclonal antibody. The substitution of B6.TNF-/- BM cells with recombinant TNF revealed promotion or suppression of BM-DC maturation depending on the point of time of TNF addition.

Item Details

Item Type:Refereed Article
Keywords:tumor necrosis factor , mouse, knockout , bone
Research Division:Medical and Health Sciences
Research Group:Immunology
Research Field:Immunology not elsewhere classified
Objective Division:Health
Objective Group:Clinical Health (Organs, Diseases and Abnormal Conditions)
Objective Field:Infectious Diseases
Author:Korner, H (Professor Heinrich Korner)
ID Code:72474
Year Published:2003
Web of Science® Times Cited:55
Deposited By:Research Division
Deposited On:2011-08-26
Last Modified:2011-12-23
Downloads:1 View Download Statistics

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