| Literature DB >> 15661904 |
Rosa Sacedón1, Blanca Díez, Vanesa Nuñez, Carmen Hernández-López, Cruz Gutierrez-Frías, Teresa Cejalvo, Susan V Outram, Tessa Crompton, Agustín G Zapata, Angeles Vicente, Alberto Varas.
Abstract
The Hedgehog (Hh) signaling pathway is involved in the development of many tissues during embryogenesis, but has also been described to function in adult self-renewing tissues. In the immune system, Sonic Hedgehog (Shh) regulates intrathymic T cell development and modulates the effector functions of peripheral CD4(+) T cells. In this study we investigate whether Shh signaling is involved in peripheral B cell differentiation in mice. Shh is produced by follicular dendritic cells, mainly in germinal centers (GCs), and GC B cells express both components of the Hh receptor, Patched and Smoothened. Blockade of the Hh signaling pathway reduces the survival, and consequently the proliferation and Ab secretion, of GC B cells. Furthermore, Shh rescues GC B cells from apoptosis induced by Fas ligation. Taken together, our data suggest that Shh is one of the survival signals provided by follicular dendritic cells to prevent apoptosis in GC B cells.Entities:
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Year: 2005 PMID: 15661904 DOI: 10.4049/jimmunol.174.3.1456
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422