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Characterization of Oct4-GFP transgenic mice as a model to study the effect of environmental estrogens on the maturation of male germ cells by using flow cytometry

•We study changes in male germ cells by exposure to xenoestrogens in Oct4/GFP mouse.•Oct4/GFP maturation profile from neonatal period until adult stage was established.•Neonatal Oct4 expression increased after perinatal exposure to ethynilestradiol.•Sperm count in adult mice was reduced after perina...

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Published in:The Journal of steroid biochemistry and molecular biology 2015-11, Vol.154, p.53-61
Main Authors: Porro, Valentina, Pagotto, Romina, Harreguy, María Belén, Ramírez, Sofía, Crispo, Martina, Santamaría, Clarisa, Luque, Enrique H., Rodríguez, Horacio A., Bollati-Fogolín, Mariela
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container_title The Journal of steroid biochemistry and molecular biology
container_volume 154
creator Porro, Valentina
Pagotto, Romina
Harreguy, María Belén
Ramírez, Sofía
Crispo, Martina
Santamaría, Clarisa
Luque, Enrique H.
Rodríguez, Horacio A.
Bollati-Fogolín, Mariela
description •We study changes in male germ cells by exposure to xenoestrogens in Oct4/GFP mouse.•Oct4/GFP maturation profile from neonatal period until adult stage was established.•Neonatal Oct4 expression increased after perinatal exposure to ethynilestradiol.•Sperm count in adult mice was reduced after perinatal exposure to ethynilestradiol.•Oct4/GFP mouse is useful to detect changes in male germ cells by xenoestrogens. Oct4 is involved in regulation of pluripotency during normal development and is down-regulated during formation of postnatal reservoir of germ cells. We propose thatOct4/GFP transgenic mouse, which mimics the endogenous expression pattern of Oct4, could be used as a mammalian model to study the effects of environmental estrogens on the development of male germ cells. Oct4/GFP maturation profile was assessed during postnatal days -PND- 3, 5, 7, 10, 14 and 80, using flow cytometry. Then, we exposed pregnant mothers to 17α-ethinylestradiol (EE2) from day post coitum (dpc) 5 to PND7. Percentage of Oct4/GFP-expressing cells and levels of expression of Oct4/GPF were increased in PND7 after EE2 exposure. These observations were confirmed by analysis of GFP and endogenous Oct4 protein in the seminiferous tubules and by a reduction in epididymal sperm count in adult mice. We introduced Oct4/GFP mouse together with flow cytometry as a tool to evaluate changes in male germ cells development.
doi_str_mv 10.1016/j.jsbmb.2015.06.006
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Oct4 is involved in regulation of pluripotency during normal development and is down-regulated during formation of postnatal reservoir of germ cells. We propose thatOct4/GFP transgenic mouse, which mimics the endogenous expression pattern of Oct4, could be used as a mammalian model to study the effects of environmental estrogens on the development of male germ cells. Oct4/GFP maturation profile was assessed during postnatal days -PND- 3, 5, 7, 10, 14 and 80, using flow cytometry. Then, we exposed pregnant mothers to 17α-ethinylestradiol (EE2) from day post coitum (dpc) 5 to PND7. Percentage of Oct4/GFP-expressing cells and levels of expression of Oct4/GPF were increased in PND7 after EE2 exposure. These observations were confirmed by analysis of GFP and endogenous Oct4 protein in the seminiferous tubules and by a reduction in epididymal sperm count in adult mice. 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Oct4 is involved in regulation of pluripotency during normal development and is down-regulated during formation of postnatal reservoir of germ cells. We propose thatOct4/GFP transgenic mouse, which mimics the endogenous expression pattern of Oct4, could be used as a mammalian model to study the effects of environmental estrogens on the development of male germ cells. Oct4/GFP maturation profile was assessed during postnatal days -PND- 3, 5, 7, 10, 14 and 80, using flow cytometry. Then, we exposed pregnant mothers to 17α-ethinylestradiol (EE2) from day post coitum (dpc) 5 to PND7. Percentage of Oct4/GFP-expressing cells and levels of expression of Oct4/GPF were increased in PND7 after EE2 exposure. These observations were confirmed by analysis of GFP and endogenous Oct4 protein in the seminiferous tubules and by a reduction in epididymal sperm count in adult mice. 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Oct4 is involved in regulation of pluripotency during normal development and is down-regulated during formation of postnatal reservoir of germ cells. We propose thatOct4/GFP transgenic mouse, which mimics the endogenous expression pattern of Oct4, could be used as a mammalian model to study the effects of environmental estrogens on the development of male germ cells. Oct4/GFP maturation profile was assessed during postnatal days -PND- 3, 5, 7, 10, 14 and 80, using flow cytometry. Then, we exposed pregnant mothers to 17α-ethinylestradiol (EE2) from day post coitum (dpc) 5 to PND7. Percentage of Oct4/GFP-expressing cells and levels of expression of Oct4/GPF were increased in PND7 after EE2 exposure. These observations were confirmed by analysis of GFP and endogenous Oct4 protein in the seminiferous tubules and by a reduction in epididymal sperm count in adult mice. 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ispartof The Journal of steroid biochemistry and molecular biology, 2015-11, Vol.154, p.53-61
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1879-1220
language eng
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source ScienceDirect Freedom Collection
subjects Animals
Environmental Pollutants - pharmacology
Estrogens
Ethinyl Estradiol - pharmacology
Flow cytometry
Gene Expression Profiling
GFP
Green Fluorescent Proteins - genetics
Male
Male germ cells
Maturation
Mice
Mice, Inbred C57BL
Mice, Transgenic
Oct4
Octamer Transcription Factor-3 - genetics
Octamer Transcription Factor-3 - physiology
Sperm Count
Sperm Motility
Spermatozoa - drug effects
title Characterization of Oct4-GFP transgenic mice as a model to study the effect of environmental estrogens on the maturation of male germ cells by using flow cytometry
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