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Uropathogenic E. coli induce different immune response in testicular and peritoneal macrophages : Implications for testicular immune privilege

Bhushan, Sudhanshu ; Hossain, Hamid ; Lu, Yongning ; Geisler, Andreas ; Tchatalbachev, Svetlin ; Mikulski, Zbigniew ; Schuler, Gerhard ; Klug, Jörg ; Pilatz, Adrian ; Wagenlehner, Florian ; Chakraborty, Trinad ; Meinhardt, Andreas


Originalveröffentlichung: (2011) PLoS ONE 6(12): e28452. doi:10.1371/journal.pone.0028452
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URN: urn:nbn:de:hebis:26-opus-85093
URL: http://geb.uni-giessen.de/geb/volltexte/2011/8509/

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Freie Schlagwörter (Englisch): male infertility , uropathogenic E. coli (UPEC) , testicular macrophages (TM) , nuclear factor of activated T cells (NFAT) signaling , cytokines
Sammlung: Open Access - Publikationsfonds
Universität Justus-Liebig-Universität Gießen
Institut: Department of Anatomy and Cell Biology, Unit of Reproductive Biology
Fachgebiet 1: Medizin fachübergreifend
Fachgebiet 2: Universität, Präsident der JLU
DDC-Sachgruppe: Medizin
Dokumentart: Aufsatz
Sprache: Englisch
Erstellungsjahr: 2011
Publikationsdatum: 19.12.2011
Kurzfassung auf Englisch: Infertility affects one in seven couples and ascending bacterial infections of the male genitourinary tract by Escherichia coli are an important cause of male factor infertility. Thus understanding mechanisms by which immunocompetent cells such as testicular macrophages (TM) respond to infection and how bacterial pathogens manipulate defense pathways is of importance. Whole genome expression profiling of TM and peritoneal macrophages (PM) infected with uropathogenic E. coli (UPEC) revealed major differences in regulated genes. However, a multitude of genes implicated in calcium signaling pathways was a common feature which indicated a role of calcium-dependent nuclear factor of activated T cells (NFAT) signaling. UPEC-dependent NFAT activation was confirmed in both cultured TM and in TM in an in vivo UPEC infectious rat orchitis model. Elevated expression of NFATC2-regulated anti-inflammatory cytokines was found in TM (IL-4, IL-13) and PM (IL-3, IL-4, IL-13). NFATC2 is activated by rapid influx of calcium, an activity delineated to the pore forming toxin alpha-hemolysin by bacterial mutant analysis. Alpha-hemolysin suppressed IL-6 and TNF-alpha cytokine release from PM and caused differential activation of MAP kinase and AP-1 signaling pathways in TM and PM leading to reciprocal expression of key pro-inflammatory cytokines in PM (IL-1alpha, IL-1beta, IL-6 downregulated) and TM (IL-1beta, IL-6 upregulated). In addition, unlike PM, LPS-treated TM were refractory to NFkappaB activation shown by the absence of degradation of IkappaBalpha and lack of pro-inflammatory cytokine secretion (IL-6, TNF-alpha). Taken together, these results suggest a mechanism to the conundrum by which TM initiate immune responses to bacteria, while maintaining testicular immune privilege with its ability to tolerate neo-autoantigens expressed on developing spermatogenic cells.
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