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Unraveling the role of lipid droplets and perilipin 2 in bovine luteal cells.
Plewes, Michele R; Talbott, Heather A; Schott, Micah B; Wood, Jennifer R; Cupp, Andrea S; Davis, John S.
Afiliación
  • Plewes MR; Olson Center for Women's Health, Department of Obstetrics and Gynecology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
  • Talbott HA; Veterans Affairs Nebraska Western Iowa Health Care System, Omaha, Nebraska, USA.
  • Schott MB; Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
  • Wood JR; Olson Center for Women's Health, Department of Obstetrics and Gynecology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
  • Cupp AS; Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
  • Davis JS; Department of Animal Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
FASEB J ; 38(11): e23710, 2024 Jun 15.
Article en En | MEDLINE | ID: mdl-38822676
ABSTRACT
Steroidogenic tissues contain cytosolic lipid droplets that are important for steroidogenesis. Perilipin 2 (PLIN2), a structural coat protein located on the surface of lipid droplets in mammalian cells, plays a crucial role in regulating lipid droplet formation and contributing to various cellular processes such as lipid storage and energy homeostasis. Herein, we examine the role that PLIN2 plays in regulating progesterone synthesis in the bovine corpus luteum. Utilizing gene array databases and Western blotting, we have delineated the expression pattern of PLIN2 throughout the follicular to luteal transition. Our findings reveal the presence of PLIN2 in both ovarian follicular and steroidogenic luteal cells, demonstrating an increase in its levels as follicular cells transition into the luteal phase. Moreover, the depletion of PLIN2 via siRNA enhanced progesterone production in small luteal cells, whereas adenovirus-mediated overexpression of both PLIN2 and Perilipin 3 (PLIN3) induced an increase in cytosolic lipid droplet accumulation and decreased hormone-induced progesterone synthesis in these cells. Lastly, in vivo administration of the luteolytic hormone prostaglandin F2α resulted in an upregulation of PLIN2 mRNA and protein expression, accompanied by a decline in serum progesterone. Our findings highlight the pivotal role of PLIN2 in regulating progesterone synthesis in the bovine corpus luteum, as supported by its dynamic expression pattern during the follicular to luteal transition and its responsiveness to luteotropic and luteolytic hormones. We suggest PLIN2 as a potential therapeutic target for modulating luteal function.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Progesterona / Perilipina-2 / Células Lúteas Límite: Animals Idioma: En Revista: FASEB J / FASEB j / FASEB journal Asunto de la revista: BIOLOGIA / FISIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Progesterona / Perilipina-2 / Células Lúteas Límite: Animals Idioma: En Revista: FASEB J / FASEB j / FASEB journal Asunto de la revista: BIOLOGIA / FISIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos