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Infection with Toxoplasma gondii results in dysregulation of the host cell cycle
Author(s) -
Molestina Robert E.,
ElGuendy Nadia,
Sinai Anthony P.
Publication year - 2008
Publication title -
cellular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.542
H-Index - 138
eISSN - 1462-5822
pISSN - 1462-5814
DOI - 10.1111/j.1462-5822.2008.01117.x
Subject(s) - biology , toxoplasma gondii , cell cycle , microbiology and biotechnology , mapk/erk pathway , cell growth , intracellular parasite , intracellular , cell , kinase , immunology , genetics , antibody
Summary Mammalian cells infected with Toxoplasma gondii are characterized by a profound reprogramming of gene expression. We examined whether such transcriptional responses were linked to changes in the cell cycle of the host. Human foreskin fibroblasts (HFFs) in the G 0 /G 1 phase of the cell cycle were infected with T. gondii and FACS analysis of DNA content was performed. Cell cycle profiles revealed a promotion into the S phase followed by an arrest towards the G 2 /M boundary with infection. This response was markedly different from that of growth factor stimulation which caused cell cycle entry and completion. Transcriptional profiles of T. gondii ‐infected HFF showed sustained increases in transcripts associated with a G 1 /S transition and DNA synthesis coupled to an abrogation of cell cycle regulators critical in G 2 /M transition relative to growth factor stimulation. These divergent responses correlated with a distinct temporal modulation of the critical cell cycle regulator kinase ERK by infection. While the kinetics of ERK phosphorylation by EGF showed rapid and sustained activation, infected cells displayed an oscillatory pattern of activation. Our results suggest that T. gondii infection induces and maintains a ‘proliferation response’ in the infected cell which may fulfill critical growth requirements of the parasite during intracellular residence.

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