Proteomic analysis of mouse ovaries during the prepubertal stages
Creators
- 1. Department of Obstetrics and Gynecology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei (China)
- 2. Department of Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei (China)
- 3. Centre for Reproductive Medicine, Puren Hospital, Wuhan University of Science and Technology, Wuhan, Hubei (China)
- 4. Hubei Key Laboratory of Embryonic Stem Cell Research, Tai-He Hospital, Hubei University of Medicine, Shiyan, Hubei (China)
Description
Highlights: • Glycoproteins such as ZP2, ZP3, Padi6, Ooep and Figla were more abundant in D7 ovary. • Energy metabolism may be related to primordial follicle activation. • Extracellular matrix metabolism plays key role on ovarian development. • Metal ion metabolism and hormone synthesis were vital during follicular development. -- Abstract: Postnatal folliculogenesis, primordial follicle activation and follicular development at early stage are important for normal ovarian function and fertility, and a comprehensive understanding of this process under physiological condition is necessary. To observe the regulation and mechanism of ovarian follicle development during the prepubertal stages, we collected the mouse ovaries from three time points, including 1 day, 7 days, and 4 weeks after birth. We then performed a proteomic analysis using tandem mass tags (TMT) labeling combined with a two-dimensional liquid chromatography-tandem mass spectrometry (2D LC-MS/MS) technique. A total of 706 proteins were determined to be significant differential abundance (P-SDA). Sixty upregulated proteins and 12 downregulated proteins that were P-SDA and 3 significant KEGG pathways (P < 0.05) were found at 7 days vs. 1 day after birth, while 237 upregulated proteins, 271 downregulated proteins and 42 significant KEGG pathways were found for 4 weeks vs. 7 days after birth. Some vital genes (Figla, Ooep, Padi6, Zp3, Hsd3b1, cyp11a1), key pathways (ECM-receptor interaction, focal adhesion, ovarian steroidogenesis, complement and coagulation cascades, PI3K/Akt/mTOR), and metabolic regulation (energy metabolism, lipid metabolism, metal ion metabolism) were found to be related to the postnatal folliculogenesis, primordial follicle activation and follicular development. Finally, qRT-PCR and western blotting verified some vital genes and further elucidated the developmental process of follicles, and the results may contribute to the understanding of the formation and activation of primordial follicle and follicular development. Significance: This study offers the first proteomic insights into mechanisms of follicle development under physiological condition during the prepubertal stages. By comparing P-SDA of mouse ovaries during various period of age, our data reveals that the regulation of primordial follicle formation and activation is significantly different from that of follicular development. These findings demonstrate that many unique molecular mechanisms underlie ovarian development could be used for ovarian disease research.
Additional details
Identifiers
- DOI
- 10.1016/j.yexcr.2019.02.016;
- PII
- S0014482719300606;
Publishing Information
- Journal Title
- Experimental Cell Research
- Journal Volume
- 377
- Journal Issue
- 1-2
- Journal Page Range
- p. 36-46
- ISSN
- 0014-4827
- CODEN
- ECREAL
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55040721
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- FERTILITY; GLYCOPROTEINS; HORMONES; LABELLING; LIPIDS; LIQUID COLUMN CHROMATOGRAPHY; MASS SPECTROSCOPY; METABOLISM; METALS; MICE; OVARIES; POLYMERASE CHAIN REACTION; RECEPTORS
- Descriptors DEC
- ANIMALS; BODY; CARBOHYDRATES; CHROMATOGRAPHY; ELEMENTS; FEMALE GENITALS; GENE AMPLIFICATION; GONADS; MAMMALS; MEMBRANE PROTEINS; ORGANIC COMPOUNDS; ORGANS; PROTEINS; RODENTS; SACCHARIDES; SEPARATION PROCESSES; SPECTROSCOPY; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2019 Elsevier Inc. All rights reserved.