- Title
- Oocyte and cumulus cell cooperativity and metabolic plasticity under the direction of oocyte paracrine factors
- Creator
- Richani, Dulama; Poljak, Anne; Bustamante, Sonia; Skerrett-Byrne, David; Harrison, Craig A.; Goldys, Ewa; Gilchrist, Robert B.; Wang, Baily; Mahbub, Saabah B.; Biazik, Joanna; Campbell, Jared M.; Habibalahi, Abbas; Stocker, William A.; Marinova, Maria B.; Nixon, Brett
- Relation
- American Journal of Physiology - Endocrinology and Metabolism Vol. 326, Issue 3, p. E366-E381
- Publisher Link
- http://dx.doi.org/10.1152/AJPENDO.00148.2023
- Publisher
- American Physiological Society
- Resource Type
- journal article
- Date
- 2024
- Description
- Mammalian oocytes develop and mature in a mutually dependent relationship with surrounding cumulus cells. The oocyte actively regulates cumulus cell differentiation and function by secreting soluble paracrine oocyte-secreted factors (OSFs). We characterized the molecular mechanisms by which two model OSFs, cumulin and BMP15, regulate oocyte maturation and cumulus-oocyte cooperativity. Exposure to these OSFs during mouse oocyte maturation in vitro altered the proteomic and multispectral autofluorescence profiles of both the oocyte and cumulus cells. In oocytes, cumulin significantly upregulated proteins involved in nuclear function. In cumulus cells, both OSFs elicited marked upregulation of a variety of metabolic processes (mostly anabolic), including lipid, nucleotide, and carbohydrate metabolism, whereas mitochondrial metabolic processes were downregulated. The mitochondrial changes were validated by functional assays confirming altered mitochondrial morphology, respiration, and content while maintaining ATP homeostasis. Collectively, these data demonstrate that cumulin and BMP15 remodel cumulus cell metabolism, instructing them to upregulate their anabolic metabolic processes, while routine cellular functions are minimized in the oocyte during maturation, in preparation for ensuing embryonic development.
- Subject
- germ-somatic cell communication; metabolic plasticity; mitochondrial function; oocyte developmental competence; paracrine signaling
- Identifier
- http://hdl.handle.net/1959.13/1505649
- Identifier
- uon:55700
- Identifier
- ISSN:0193-1849
- Language
- eng
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