Chronic mTOR inhibition in mice with rapamycin alters T, B, myeloid, and innate lymphoid cells and gut flora and prolongs life of immune-deficient mice.

Saved in:
Bibliographic Details
Title: Chronic mTOR inhibition in mice with rapamycin alters T, B, myeloid, and innate lymphoid cells and gut flora and prolongs life of immune-deficient mice.
Authors: Hurez V; Department of Medicine, University of Texas Health Science Center, San Antonio, TX, USA., Dao V; Graduate School of Biomedical Sciences, University of Texas Health Science Center, San Antonio, TX, USA., Liu A; Department of Medicine, University of Texas Health Science Center, San Antonio, TX, USA., Pandeswara S; Department of Medicine, University of Texas Health Science Center, San Antonio, TX, USA., Gelfond J; Department of Epidemiology and Biostatistics, University of Texas Health Science Center, San Antonio, TX, USA., Sun L; Graduate School of Biomedical Sciences, University of Texas Health Science Center, San Antonio, TX, USA., Bergman M; Graduate School of Biomedical Sciences, University of Texas Health Science Center, San Antonio, TX, USA., Orihuela CJ; Graduate School of Biomedical Sciences, University of Texas Health Science Center, San Antonio, TX, USA., Galvan V; Graduate School of Biomedical Sciences, University of Texas Health Science Center, San Antonio, TX, USA.; Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX, USA.; Department of Physiology, University of Texas Health Science Center, San Antonio, TX, USA., Padrón Á; Department of Medicine, University of Texas Health Science Center, San Antonio, TX, USA., Drerup J; Graduate School of Biomedical Sciences, University of Texas Health Science Center, San Antonio, TX, USA., Liu Y; Department of Medicine, University of Texas Health Science Center, San Antonio, TX, USA., Hasty P; Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX, USA.; Department of Molecular Medicine, Institute of Biotechnology, University of Texas Health Science Center, San Antonio, TX, USA., Sharp ZD; Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX, USA., Curiel TJ; Department of Medicine, University of Texas Health Science Center, San Antonio, TX, USA.; Graduate School of Biomedical Sciences, University of Texas Health Science Center, San Antonio, TX, USA.; Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX, USA.; Cancer Therapy & Research Center, University of Texas Health Science Center, San Antonio, TX, USA.
Source: Aging cell [Aging Cell] 2015 Dec; Vol. 14 (6), pp. 945-56. Date of Electronic Publication: 2015 Aug 28.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101130839 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1474-9726 (Electronic) Linking ISSN: 14749718 NLM ISO Abbreviation: Aging Cell Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1474-9726
DOI:10.1111/acel.12380