Academic Journal

A lipopeptide facilitate induction of Mycobacterium leprae killing in host cells.

التفاصيل البيبلوغرافية
العنوان: A lipopeptide facilitate induction of Mycobacterium leprae killing in host cells.
المؤلفون: Yumi Maeda, Toshiki Tamura, Yasuo Fukutomi, Tetsu Mukai, Masanori Kai, Masahiko Makino
المصدر: PLoS Neglected Tropical Diseases, Vol 5, Iss 11, p e1401 (2011)
بيانات النشر: Public Library of Science (PLoS), 2011.
سنة النشر: 2011
المجموعة: LCC:Arctic medicine. Tropical medicine
LCC:Public aspects of medicine
مصطلحات موضوعية: Arctic medicine. Tropical medicine, RC955-962, Public aspects of medicine, RA1-1270
الوصف: Little is known of the direct microbicidal activity of T cells in leprosy, so a lipopeptide consisting of the N-terminal 13 amino acids lipopeptide (LipoK) of a 33-kD lipoprotein of Mycobacterium leprae, was synthesized. LipoK activated M. leprae infected human dendritic cells (DCs) to induce the production of IL-12. These activated DCs stimulated autologous CD4+ or CD8+ T cells towards type 1 immune response by inducing interferon-gamma secretion. T cell proliferation was also evident from the CFSE labeling of target CD4+ or CD8+ T cells. The direct microbicidal activity of T cells in the control of M. leprae multiplication is not well understood. The present study showed significant production of granulysin, granzyme B and perforin from these activated CD4+ and CD8+ T cells when stimulated with LipoK activated, M. leprae infected DCs. Assessment of the viability of M. leprae in DCs indicated LipoK mediated T cell-dependent killing of M. leprae. Remarkably, granulysin as well as granzyme B could directly kill M. leprae in vitro. Our results provide evidence that LipoK could facilitate M. leprae killing through the production of effector molecules granulysin and granzyme B in T cells.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1935-2735
Relation: http://europepmc.org/articles/PMC3222628?pdf=render; https://doaj.org/toc/1935-2735
DOI: 10.1371/journal.pntd.0001401
URL الوصول: https://doaj.org/article/54b80051cdb74e6db95a50dfcc07424d
رقم الانضمام: edsdoj.54b80051cdb74e6db95a50dfcc07424d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:19352735
DOI:10.1371/journal.pntd.0001401