Author/Authors :
Jafari, Reza School of Medicine - Shahroud University of Medical Sciences, Shahroud, Iran , Taghavi, Abdolvahab Fertility and Infertility Research Center - Hormozgan University of Medical Sciences, Bandarabbas, Iran , Amirchaghmaghi, Elham Department of Endocrinology and Female Infertility - Reproductive Biomedicine Research Center - Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran , Salman Yazdi, Reza Department of Andrology - Reproductive Biomedicine Research Center - Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran , Karimian, Leili Department of Embryology - Reproductive Biomedicine Research Center - Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran , Ashrafi, Mahnaz Department of Endocrinology and Female Infertility - Reproductive Biomedicine Research Center - Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran , Aflatoonian, Reza Department of Gynecology and Obstetrics - School of Medicine - Yasuj University of Medical Sciences, Yasuj, Iran
Abstract :
Background: Inflammatory responses within the peritoneal cavity may result in endometrial
dysfunction in women with endometriosis. The true causes of this disease
remain poorly understood. It is hypothesized that downstream toll-like receptors
(TLRs) inflammatory cytokines in response to pathogens may be associated with endometriosis.
So, this study was aimed at evaluating the expression of TLRs signaling
and endometriosis-associated inflammatory responses.
Methods: Totally, 20 infertile endometriosis patients and 20 normal women undergoing
controlled ovarian stimulation were enrolled. The cellular pellet and supernatant
were obtained by centrifugation of follicular fluid (FF). Evaluation of TLRs and
their signaling pathway gene expression was performed on cellular pellets using
quantitative-PCR. The supernatant was used for determination of cytokine protein
expression by ELISA. The results are expressed as mean±SEM and a p<0.05 was
considered statistically significant.
Results: Quantitative-PCR analysis suggested that TLR1, 5, 6, 7, 8, 10, MYD88,
NF-ĸB, IL-10 and TGF-β genes expression significantly increased in patients compared
to the control group (p<0.05). TLR3, 9, INF-β genes expression was significantly
lower in endometriosis than control group (p<0.05). There was no significant
difference in the expression of TLR2, TLR4, TIRAP, TRIF, TRAM, and IRF3 between
two groups. Also, significant increase in the levels of IL-6, IL-8 and MIF protein
in FF of endometriosis group was detected in comparison with normal women
(p<0.05).
Conclusion: The expression of TLR downstream signaling in the follicular cells can
initiate inflammatory responses and changes in the FF cytokine profile which in turn
may induce endometriosis and infertility disorder
Keywords :
Endometriosis , Follicular cells , Infertility , Inflammation , TLR