2011
DOI: 10.1016/j.contraception.2011.06.006
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Differential regulation of endogenous pro-inflammatory cytokine genes by medroxyprogesterone acetate and norethisterone acetate in cell lines of the female genital tract

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Cited by 51 publications
(45 citation statements)
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“…However, the relative affinities of P 4 and MPA for the GR may be different in this cell line compared with other cell lines, as it has previously been shown that the concentration of GR determines the binding affinity of a ligand for the receptor (93). Moreover, as we have previously shown that P 4 and MPA differentially regulate cytokine gene expression in a cell-and promoter-specific manner (39), discrepancies between the results from this study and others using synthetic GRE-containing promoters in COS-1 cells, for example (11), may be due to either cell-or promoter-specific effects.…”
Section: Discussionmentioning
confidence: 95%
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“…However, the relative affinities of P 4 and MPA for the GR may be different in this cell line compared with other cell lines, as it has previously been shown that the concentration of GR determines the binding affinity of a ligand for the receptor (93). Moreover, as we have previously shown that P 4 and MPA differentially regulate cytokine gene expression in a cell-and promoter-specific manner (39), discrepancies between the results from this study and others using synthetic GRE-containing promoters in COS-1 cells, for example (11), may be due to either cell-or promoter-specific effects.…”
Section: Discussionmentioning
confidence: 95%
“…These cells were used as an in vitro cell culture model for mucosal immunity in the female ectocervical environment, as they closely resemble the characteristics of their tissue of origin and primary cells (39,47). An increase in pro-inflammatory cytokines such as IL-12 is critical for the progression of inflammation, although anti-inflammatory cytokines such as IL-10 control the course of the inflammatory process (45,(53)(54)(55)(56).…”
Section: Resultsmentioning
confidence: 99%
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“…Different regions of the genital tract have different thicknesses of the protective epithelial layers, and have varying types and amounts of submucosal immune cells. A differential response to the same immunologic stimuli has been reported, [19][20][21][22] and regionally dependent susceptibility to HIV-1 infection has been suggested among different parts of the lower genital tract. The endocervix as well as the transformation zone between the endocervix and ectocervix were more vulnerable to HIV-1 infection compared to the ectocervix and vagina as examined in a macaque model.…”
Section: Introductionmentioning
confidence: 91%