Mycobacterium tuberculosis–Induced Apoptosis in Monocytes/Macrophages: Early Membrane Modifications and Intracellular Mycobacterial Viability
Author(s) -
Marilina B. Santucci,
Massimo Amicosante,
Rosella Cicconi,
Carla Montesano,
M Casarini,
S Giosuè,
A Bisetti,
Vittorio Colizzi,
Maurizio Fraziano
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315371
Subject(s) - apoptosis , cd14 , annexin a5 , mycobacterium tuberculosis , macrophage , annexin , biology , monocyte , viability assay , microbiology and biotechnology , in vitro , intracellular , tuberculosis , immunology , immune system , medicine , biochemistry , pathology
Apoptosis has been observed in monocytes/macrophages in the course of in vivo and in vitro Mycobacterium tuberculosis (MTB) infection. In order to define the early events of MTB-induced apoptosis, membrane CD14 expression and the exposure of Annexin V-binding sites in MTB-infected monocytes/macrophages have been monitored. Moreover, the role of MTB-induced apoptosis was further analyzed in vitro in terms of mycobacterial viability. Results show that monocyte/macrophage apoptosis is a very early event that is strictly dependent on the MTB amount, and this apoptosis is associated with a selective down-regulation of surface CD14 expression. Furthermore, no statistically significant decrease in mycobacterial viability was observed, which indicates that the apoptotic pathway triggered by high doses of MTB is associated with parasite survival rather than with killing of the parasite.
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