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Effect of retinoic acid on apoptosis and expression of Fas proteins in mouse blastocysts cultured in vitro / 华中科技大学学报(医学)(英德文版)
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 239-42, 2008.
Article in English | WPRIM | ID: wpr-634604
ABSTRACT
Mouse blastocysts were exposed to doses of 0, 1 and 10 mumol/L retinoic acid (RA) for 24 h and the cytotoxic effect of RA on the mouse blastocysts in vitro was observed. FITC-labeled terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL-FITC) assay was employed to stain apoptotic cells and immunohistochemical S-P staining method was used to detect the expression of Fas protein in mouse blastocysts in vitro. The results showed that RA could induce apoptosis and increase the expression of Fas proteins of trophectoderm (TE) and inner cell mass (ICM) cells in blastocysts. Compared with the findings for the control blastocysts, exposure to RA (10 mumol/L) resulted in a more significant apoptosis and higher expression level of Fas proteins (P<0.01). It was concluded that RA could induce apoptosis, which may result in a significant reduction in the average number of total cells and the trophectoderm/inner cell mass in blastocysts and an increased expression of Fas protein, suggesting that RA had a cytotoxic effect on the growth and development of early embryos in mice.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Tretinoin / Blastocyst / RNA, Messenger / Cells, Cultured / Gene Expression Regulation / Apoptosis / Cell Culture Techniques / Fas Receptor / In Situ Nick-End Labeling Language: English Journal: Journal of Huazhong University of Science and Technology (Medical Sciences) Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Tretinoin / Blastocyst / RNA, Messenger / Cells, Cultured / Gene Expression Regulation / Apoptosis / Cell Culture Techniques / Fas Receptor / In Situ Nick-End Labeling Language: English Journal: Journal of Huazhong University of Science and Technology (Medical Sciences) Year: 2008 Type: Article