Journal of Medical Microbiology · 2005 · 23 citations · 20 references
Life SciencesCell BiologyMicrobiologyApoptosisMedical MicrobiologyMicrobial PathogenesisApoptosis In Immune CellsApoptosis RegulationApoptotic Signal TransductionApoptotic SignalingCell DeathMacrophage BiologyApoptosis In Bacterial InfectionApoptosis In Cell CultureApoptosis In InfectionApoptosis Regulation By KinasesLactate Dehydrogenase Release AssaysMap Kinase-mediated Apoptotic SignalingMapk SignalingMitogen-activated Protein Kinase Signaling
It has previously been reported that the murine macrophage cell line J774.1 and the human oral epithelial cell line KB undergo apoptosis as a result of Actinobacillus actinomycetemcomitans infection. Recent studies have demonstrated that apoptosis regulation is modulated by multiple phosphorylation of several different protein kinases, including the major subtypes of the mitogen-activated protein kinase (MAPK) family. The MAPK family promotes cell survival and/or proliferation in response to growth factor stimulation, or apoptosis in response to various stress stimuli. The primary objective of the present investigation was to clarify whether human immune cells undergo apoptosis following A. actinomycetemcomitans infection and, if so, to establish the involvement of the MAPK family. Human monocytic THP-1 cells were infected with A. actinomycetemcomitans in microtubes. Lactate dehydrogenase release into the culture supernatant and DNA fragmentation in the cells were monitored. DNA fragmentation was also identified by agarose gel electrophoresis. Cell death following A. actinomycetemcomitans infection occurred by apoptosis, shown by an increase in the proportion of fragmented DNA and the typical ladder pattern of DNA fragmentation indicative of apoptosis. Furthermore, p38 MAPK activity and tumour necrosis factor alpha (TNF-alpha) levels increased following A. actinomycetemcomitans infection. In contrast, cell death and TNF-alpha levels in infected cells decreased upon addition of a p38 inhibitor or an anti-TNF-alpha antibody. However, exogenous TNF-alpha could not induce apoptosis in uninfected THP-1 cells. Interestingly, p38 MAPK activity diminished in the presence of anti-TNF-alpha antibody. These findings indicated that A. actinomycetemcomitans infection induces apoptosis in THP-1 cells and that p38 MAPK activity is directly involved in apoptosis. TNF-alpha may play an indirect role in apoptosis via enhanced p38 MAPK activity. A. actinomycetemcomitans-induced apoptosis of human immune cells may be important in terms of initiation and progression of periodontal diseases.
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The stress-activated protein kinase subfamily of c-Jun kinases
John Kyriakis, Papia T. Banerjee, Eleni Nikolakaki et al. · Nature · 1994 · 2.6K citations
Anthony G. Molloy, Pairote Laochumroonvorapong, Gilla Kaplan · The Journal of Experimental Medicine · 1994 · 508 citations · Full text
Jonathan L. E. Dean, Matthew Brook, Andrew R. Clark et al. · Journal of Biological Chemistry · 1999 · 492 citations · Full text
Neal I. Walker, Brian Harmon, G. Gobe et al. · PubMed · 1988 · 464 citations
Silke Hobbie, Li-Mei Chen, Roger J. Davis et al. · The Journal of Immunology · 1997 · 408 citations