In vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of AMPK and cause of infertility

Abstract Background Mural granulosa cells from IVF patients were provided by the West Virginia University Center for Reproductive Medicine in Morgantown, WV. The effect of adenosine monophosphate activated protein kinase (AMPK) activation, primary cause of infertility, age, BMI, and pregnancy outcom...

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Main Authors: E. C. Bowdridge, M. W. Vernon, J. A. Flores, M. J. Clemmer
Format: Article
Language:English
Published: BMC 2017-09-01
Series:Reproductive Biology and Endocrinology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12958-017-0295-9
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spelling doaj-1544f7a5ac7b497d93abf6b8762ccdd22020-11-25T00:35:18ZengBMCReproductive Biology and Endocrinology1477-78272017-09-011511810.1186/s12958-017-0295-9In vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of AMPK and cause of infertilityE. C. Bowdridge0M. W. Vernon1J. A. Flores2M. J. Clemmer3Department of Physiology and Pharmacology, West Virginia UniversityDepartment of Obstetrics and Gynecology, West Virginia UniversityDepartment of Biology West Virginia UniversityDepartment of Obstetrics and Gynecology, West Virginia UniversityAbstract Background Mural granulosa cells from IVF patients were provided by the West Virginia University Center for Reproductive Medicine in Morgantown, WV. The effect of adenosine monophosphate activated protein kinase (AMPK) activation, primary cause of infertility, age, BMI, and pregnancy outcome on production of progesterone were examined separately. Methods Isolated mural sheets from IVF patients (n = 26) were centrifuged, supernatant discarded, and the pellet re-suspended in 500 μl of DMEM/F12. Mural granulosa cells were plated at 10,000 cells/well in triplicate per treatment group with 300 μl DMEM/F12 media at 37 °C and 5% CO2 in a humidified incubator to permit luteinization. Four days after initial plating, cells were treated with either an AMPK inhibitor, DM; an AMPK activator, AICAR; or hCG. Cells were cultured for 24 h after treatment when medium was collected and frozen at −20 °C until assayed for P4 by radioimmunoassay. Results The AMPK activator, AICAR, inhibited P4 production (P < 0.001), whereas the AMPK inhibitor, DM, did not affect basal P4 (P < 0.05). Progesterone production increased when cells from patients whose primary cause of infertility was a partner having male infertility were treated with hCG compared to control (P = 0.0045), but not in patients with other primary infertility factors (P > 0.05). Additionally, hCG increased P4 production in patients between the ages 30–35 (P = 0.008) and 36–39 (P = 0.04), but not in patients ages 25–29 (P = 0.73). Patients with normal BMI had increased P4 production when treated with hCG (P < 0.0001), however there was no change in P4 production from cells of patients who were overweight or obese (P > 0.05). Cells from patients who became pregnant to IVF had greater P4 production when stimulated with hCG than those who did not become pregnant when compared to controls (P > 0.05). Conclusions Understanding how AMPK activation is regulated in ovarian cells could lead to alternative or novel infertility treatments. Human mural granulosa cells can serve as a valuable model for understanding how AMPK affects P4 production in steroidogenic cells. Additionally, when stimulated with hCG, P4 production by mural granulosa cells differed among infertility type, age, BMI, and pregnancy outcome.http://link.springer.com/article/10.1186/s12958-017-0295-9Granulosa cellsPregnancyLuteal insufficiency
collection DOAJ
language English
format Article
sources DOAJ
author E. C. Bowdridge
M. W. Vernon
J. A. Flores
M. J. Clemmer
spellingShingle E. C. Bowdridge
M. W. Vernon
J. A. Flores
M. J. Clemmer
In vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of AMPK and cause of infertility
Reproductive Biology and Endocrinology
Granulosa cells
Pregnancy
Luteal insufficiency
author_facet E. C. Bowdridge
M. W. Vernon
J. A. Flores
M. J. Clemmer
author_sort E. C. Bowdridge
title In vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of AMPK and cause of infertility
title_short In vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of AMPK and cause of infertility
title_full In vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of AMPK and cause of infertility
title_fullStr In vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of AMPK and cause of infertility
title_full_unstemmed In vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of AMPK and cause of infertility
title_sort in vitro progesterone production by luteinized human mural granulosa cells is modulated by activation of ampk and cause of infertility
publisher BMC
series Reproductive Biology and Endocrinology
issn 1477-7827
publishDate 2017-09-01
description Abstract Background Mural granulosa cells from IVF patients were provided by the West Virginia University Center for Reproductive Medicine in Morgantown, WV. The effect of adenosine monophosphate activated protein kinase (AMPK) activation, primary cause of infertility, age, BMI, and pregnancy outcome on production of progesterone were examined separately. Methods Isolated mural sheets from IVF patients (n = 26) were centrifuged, supernatant discarded, and the pellet re-suspended in 500 μl of DMEM/F12. Mural granulosa cells were plated at 10,000 cells/well in triplicate per treatment group with 300 μl DMEM/F12 media at 37 °C and 5% CO2 in a humidified incubator to permit luteinization. Four days after initial plating, cells were treated with either an AMPK inhibitor, DM; an AMPK activator, AICAR; or hCG. Cells were cultured for 24 h after treatment when medium was collected and frozen at −20 °C until assayed for P4 by radioimmunoassay. Results The AMPK activator, AICAR, inhibited P4 production (P < 0.001), whereas the AMPK inhibitor, DM, did not affect basal P4 (P < 0.05). Progesterone production increased when cells from patients whose primary cause of infertility was a partner having male infertility were treated with hCG compared to control (P = 0.0045), but not in patients with other primary infertility factors (P > 0.05). Additionally, hCG increased P4 production in patients between the ages 30–35 (P = 0.008) and 36–39 (P = 0.04), but not in patients ages 25–29 (P = 0.73). Patients with normal BMI had increased P4 production when treated with hCG (P < 0.0001), however there was no change in P4 production from cells of patients who were overweight or obese (P > 0.05). Cells from patients who became pregnant to IVF had greater P4 production when stimulated with hCG than those who did not become pregnant when compared to controls (P > 0.05). Conclusions Understanding how AMPK activation is regulated in ovarian cells could lead to alternative or novel infertility treatments. Human mural granulosa cells can serve as a valuable model for understanding how AMPK affects P4 production in steroidogenic cells. Additionally, when stimulated with hCG, P4 production by mural granulosa cells differed among infertility type, age, BMI, and pregnancy outcome.
topic Granulosa cells
Pregnancy
Luteal insufficiency
url http://link.springer.com/article/10.1186/s12958-017-0295-9
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