Oocyte and cumulus cell cooperativity and metabolic plasticity under the direction of oocyte paracrine factors

Author:

Richani Dulama1,Poljak Anne2,Wang Baily1,Mahbub Saabah B.3,Biazik Joanna4,Campbell Jared M.3,Habibalahi Abbas3,Stocker William A.5,Marinova Maria B.1,Nixon Brett6,Bustamante Sonia7,Skerrett-Byrne David6,Harrison Craig A.8,Goldys Ewa3,Gilchrist Robert B.9

Affiliation:

1. Discipline of Women's Health, School of Clinical Medicine, University of New South Wales Sydney, Australia

2. Bioanalytical Mass Spectrometry Facility, UNSW Sydney, Sydney, New South Wales, Australia

3. Graduate School of Biomedical Engineering, University of New South Wales Sydney, Australia

4. Electron Microscope Unit, University of New South Wales Sydney, Australia

5. Department of Physiology, Monash University, Australia

6. Priority Research Centre for Reproductive Science, University of Newcastle, Australia

7. Bioanalytical Mass Spectrometry Facility, University of New South Wales Sydney, Australia

8. Monash University, Clayton, Australia

9. Discipline of Women's Health, School of Clinical Medicine, UNSW Sydney, Sydney, NSW, Australia

Abstract

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, while mitochondrial metabolic processes were downregulated. The mitochondrial changes were validated by functional assays confirming altered mitochondrial morphology, respiration, and content, whilst 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.

Funder

DHAC | National Health and Medical Research Council

Open Philanthropy Project

Publisher

American Physiological Society

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