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Role of tissue factor in Mycobacterium tuberculosis-induced inflammation and disease pathogenesis.

Title: Role of tissue factor in Mycobacterium tuberculosis-induced inflammation and disease pathogenesis.
Authors: Kothari H; Department of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, TX 75708, United States of America.; Keshava S; Department of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, TX 75708, United States of America.; Vatsyayan R; Department of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, TX 75708, United States of America.; Mackman N; Division of Hematology and Oncology, McAllister Heart Institute, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill NC 27599, United States of America.; Rao LV; Department of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, TX 75708, United States of America.; Pendurthi UR; Department of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, TX 75708, United States of America.
Source: PloS one [PLoS One] 2014 Dec 02; Vol. 9 (12), pp. e114141. Date of Electronic Publication: 2014 Dec 02 (Print Publication: 2014).
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Language: English
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
Imprint Name(s): Original Publication: San Francisco, CA : Public Library of Science
MeSH Terms: Inflammation/*etiology ; Mycobacterium tuberculosis/*pathogenicity ; Thromboplastin/*physiology ; Tuberculosis/*physiopathology; Tuberculosis/complications ; Animals ; Bronchoalveolar Lavage Fluid ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic
Abstract: Tuberculosis (TB) is a chronic lung infectious disease characterized by severe inflammation and lung granulomatous lesion formation. Clinical manifestations of TB include hypercoagulable states and thrombotic complications. We previously showed that Mycobacterium tuberculosis (M.tb) infection induces tissue factor (TF) expression in macrophages in vitro. TF plays a key role in coagulation and inflammation. In the present study, we investigated the role of TF in M.tb-induced inflammatory responses, mycobacterial growth in the lung and dissemination to other organs. Wild-type C57BL/6 and transgenic mice expressing human TF, either very low levels (low TF) or near to the level of wild-type (HTF), in place of murine TF were infected with M.tb via aerosol exposure. Levels of TF expression, proinflammatory cytokines and thrombin-antithrombin complexes were measured post M.tb infection and mycobacterial burden in the tissue homogenates were evaluated. Our results showed that M.tb infection did not increase the overall TF expression in lungs. However, macrophages in the granulomatous lung lesions in all M.tb-infected mice, including low TF mice, showed increased levels of TF expression. Conspicuous fibrin deposition in the granuloma was detected in wild-type and HTF mice but not in low TF mice. M.tb infection significantly increased expression levels of cytokines IFN-γ, TNF-α, IL-6 and IL-1ß in lung tissues. However, no significant differences were found in proinflammatory cytokines among the three experimental groups. Mycobacterial burden in lungs and dissemination into spleen and liver were essentially similar in all three genotypes. Our data indicate, in contrast to that observed in acute bacterial infections, that TF-mediated coagulation and/or signaling does not appear to contribute to the host-defense in experimental tuberculosis.
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Grant Information: R01 HL058869 United States HL NHLBI NIH HHS; HL1074830 United States HL NHLBI NIH HHS
Substance Nomenclature: 9035-58-9 (Thromboplastin)
Entry Date(s): Date Created: 20141203 Date Completed: 20160108 Latest Revision: 20210103
Update Code: 20260130
PubMed Central ID: PMC4252100
DOI: 10.1371/journal.pone.0114141
PMID: 25462128
Database: MEDLINE

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't