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Cell Physiol Biochem ; 41(3): 1083-1097, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28245469

RESUMO

BACKGROUND/AIMS: Uterine rudiments from patients with Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) contain all tissues typically found in the uterus. Endometrium from the rudiments predominantly exhibits basalis-like features, and endometrial proliferative capacity in patients' epithelium and stroma is significantly lower. METHODS: This single-center, prospective study conducted at a major German university hospital compared in-vitro decidualization in cultured ESCs from MRKHS patients and hysterectomy controls. Primary ESC cultures were established from both sources. Hormone-induced prolactin and IGFBP-1 secretion served as a measure of their ability to undergo decidualization in response to hormonal stimulation. Expression levels of 8 key marker genes of decidualization were also determined. RESULTS: At day 9, mean secretion of prolactin and IGFBP-1 was significantly reduced by 89.0% and 99.5%, respectively, in MRKHS ESCs vs. hysterectomy controls, both indicating impaired decidualization of MRKHS ESCs. Key decidual markers confirmed impaired decidualization in MRKHS patients. CONCLUSION: Our results indicate that the ESCs from MRKHS patients lack hormone responsiveness as a potential sign of dysfunctional hormone receptor function, which may also play a role in the onset of MRKHS. Further studies are needed to corroborate our findings, directly address receptor function, and elucidate the role of other potential determinants of uterine development and adult function.


Assuntos
Endométrio/anormalidades , Ductos Paramesonéfricos/anormalidades , Células Estromais/patologia , Vagina/anormalidades , Transtornos 46, XX do Desenvolvimento Sexual/metabolismo , Transtornos 46, XX do Desenvolvimento Sexual/cirurgia , Adolescente , Adulto , Anormalidades Congênitas/metabolismo , Anormalidades Congênitas/cirurgia , Endométrio/metabolismo , Endométrio/cirurgia , Estradiol/farmacologia , Feminino , Expressão Gênica/efeitos dos fármacos , Humanos , Proteína 1 de Ligação a Fator de Crescimento Semelhante à Insulina/biossíntese , Proteína 1 de Ligação a Fator de Crescimento Semelhante à Insulina/genética , Ductos Paramesonéfricos/metabolismo , Ductos Paramesonéfricos/cirurgia , Cultura Primária de Células , Progesterona/farmacologia , Prolactina/biossíntese , Prolactina/genética , Estudos Prospectivos , Células Estromais/efeitos dos fármacos , Células Estromais/metabolismo , Vagina/metabolismo , Vagina/cirurgia
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