Identification of a novel antigen cross-presenting cell type in spleen

29Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Antigen-presenting cells (APC), like dendritic cells (DC), are essential for T-cell activation, leading to immunity or tolerance. Multiple DC subsets each play a unique role in the immune response. Here, a novel splenic dendritic-like APC has been characterized in mice that has immune function and cell surface phenotype distinct from other, described DC subsets. These were identified as a cell type continuously produced in spleen long-term cultures (LTC) and have anin vivoequivalent cell type in mice, namely 'L-DC'. This study characterizes LTC-DC in terms of marker phenotype and function, and compares them with L-DC and other known splenic DC and myeloid subsets. L-DC display a myeloid dendritic-like phenotype equivalent to LTC-DC as CD11c loCD11b hiMHC-II -CD8α - cells, distinct by high accessibility and endocytic capacity for blood-borne antigen. Both LTC-DC and L-DC have strong antigen cross-presentation ability leading to strong activation of CD8 + T cells, particularly after exposure to lipopolysaccharide. However, they have weak ability to stimulate CD4 + T cells in antigen-specific responses. Evidence is presented here for a novel DC type produced byin vitrohaematopoiesis which has distinct antigen-presenting potential and reflects a DC subset present alsoin vivoin spleen. © 2011 The Authors Journal of Cellular and Molecular Medicine © 2011 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd.

Cite

CITATION STYLE

APA

Tan, J. K. H., Quah, B. J. C., Griffiths, K. L., Periasamy, P., Hey, Y. Y., & O’Neill, H. C. (2011). Identification of a novel antigen cross-presenting cell type in spleen. Journal of Cellular and Molecular Medicine, 15(5), 1189–1199. https://doi.org/10.1111/j.1582-4934.2010.01089.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free