| Literature DB >> 22921121 |
Alan M Hanash1, Jarrod A Dudakov, Guoqiang Hua, Margaret H O'Connor, Lauren F Young, Natalie V Singer, Mallory L West, Robert R Jenq, Amanda M Holland, Lucy W Kappel, Arnab Ghosh, Jennifer J Tsai, Uttam K Rao, Nury L Yim, Odette M Smith, Enrico Velardi, Elena B Hawryluk, George F Murphy, Chen Liu, Lynette A Fouser, Richard Kolesnick, Bruce R Blazar, Marcel R M van den Brink.
Abstract
Little is known about the maintenance of intestinal stem cells (ISCs) and progenitors during immune-mediated tissue damage or about the susceptibility of transplant recipients to tissue damage mediated by the donor immune system during graft versus host disease (GVHD). We demonstrate here that deficiency of recipient-derived IL-22 increased acute GVHD tissue damage and mortality, that ISCs were eliminated during GVHD, and that ISCs as well as their downstream progenitors expressed the IL-22 receptor. Intestinal IL-22 was produced after bone marrow transplant by IL-23-responsive innate lymphoid cells (ILCs) from the transplant recipients, and intestinal IL-22 increased in response to pretransplant conditioning. However, ILC frequency and IL-22 amounts were decreased by GVHD. Recipient IL-22 deficiency led to increased crypt apoptosis, depletion of ISCs, and loss of epithelial integrity. Our findings reveal IL-22 as a critical regulator of tissue sensitivity to GVHD and a protective factor for ISCs during inflammatory intestinal damage.Entities:
Mesh：
Substances：
Year: 2012 PMID： 22921121 PMCID： PMC3477611 DOI： 10.1016/j.immuni.2012.05.028
Source DB: PubMed Journal: Immunity ISSN： 1074-7613 Impact factor: 31.745