Role of insulin-like growth factor 1 (IGF1) in the regulation of mitochondrial bioenergetics in zebrafish oocytes: lessons from in vivo and in vitro investigations

Optimal mitochondrial functioning is indispensable for acquiring oocyte competence and meiotic maturation, whilst mitochondrial dysfunction may lead to diminished reproductive potential and impaired fertility. The role of the intra-ovarian IGF system in ovarian follicular dynamics has been implicated earlier. Although several studies have demonstrated the role of the IGF axis in facilitating mitochondrial function over a multitude of cell lines, its role in oocyte energy metabolism remains largely unexplored. Here using zebrafish, the relative importance of IGF1 in modulating oocyte mitochondrial bioenergetics has been investigated. A dramatic increase in ovarian lhcgr and igf1 expression accompanied heightened ATP levels and mitochondrial polarization in full-grown (FG) oocytes resuming meiotic maturation and ovulation in vivo. Concomitant with elevated igf1 expression and IGF1R phosphorylation, hCG (LH analog) stimulation of FG follicles in vitro prompted a sharp increase in NRF-1 and ATP levels, suggesting a positive influence of gonadotropin action on igf1 expression vis-à-vis oocyte bioenergetics. While recombinant IGF1 administration enhanced mitochondrial function, IGF1R immunodepletion or priming with PI3K inhibitor wortmannin could abrogate NRF-1 immunoreactivity, expression of respiratory chain subunits, ΔΨM, and ATP content. Mechanistically, activation of PI3K/Akt signaling in IGF1-treated follicles corroborated well with the rapid phosphorylation of GSK3β at Ser9 (inactive) followed by PGC-1β accumulation. While selective inhibition of GSK3β promoted PGC-1β, Akt inhibition could abrogate IGF1-induced p-GSK3β (Ser9) and PGC-1β immunoreactive protein indicating Akt-mediated GSK3β inactivation and PGC-1β stabilization. The IGF1-depleted follicles showed elevated superoxide anions, subdued steroidogenic potential, and attenuated G2-M1 transition. In summary, this study highlights the importance of IGF1 signaling in oocyte bioenergetics prior to resumption of meiosis.

[1]  Parivash Afradiasbagharani,et al.  The insulin-like growth factor and its players: their functions, significance, and consequences in all aspects of ovarian physiology , 2022, Middle East Fertility Society Journal.

[2]  M. Martínez-Zamora,et al.  Oocytes maintain ROS-free mitochondrial metabolism by suppressing complex I , 2022, Nature.

[3]  D. Adhikari,et al.  Oocyte mitochondria—key regulators of oocyte function and potential therapeutic targets for improving fertility , 2022, Biology of Reproduction.

[4]  J. Smitz,et al.  The Role of Mitochondria in Oocyte Maturation , 2021, Cells.

[5]  Subhasri Biswas,et al.  Altered redox homeostasis in steroid-depleted follicles attenuates hCG regulation of follicular events: Cross-talk between endocrine and IGF axis in maturing oocytes. , 2021, Free radical biology & medicine.

[6]  Oxford Textbook of Endocrinology and Diabetes 3e , 2021 .

[7]  A. Gambineri,et al.  Exogenous Factors and Female Reproductive Health , 2021, Oxford Textbook of Endocrinology and Diabetes 3e.

[8]  F. Amicarelli,et al.  Mitochondrial Sirtuins in Reproduction , 2021, Antioxidants.

[9]  U. Mukherjee,et al.  Bisphenol A impairs reproductive fitness in zebrafish ovary: Potential involvement of oxidative/nitrosative stress, inflammatory and apoptotic mediators. , 2020, Environmental pollution.

[10]  H. Habibi,et al.  Role of GnRH and GnIH in paracrine/autocrine control of final oocyte maturation. , 2020, General and comparative endocrinology.

[11]  T. Tokumoto,et al.  An agonist for membrane progestin receptor (mPR) induces oocyte maturation and ovulation in zebrafish in vivo. , 2020, Biochemical and biophysical research communications.

[12]  N. Dekel,et al.  Newly Identified Regulators of Ovarian Folliculogenesis and Ovulation , 2020, International journal of molecular sciences.

[13]  R. Bezerra,et al.  Mitochondria as targets for toxicity and metabolism research using zebrafish. , 2020, Biochimica et biophysica acta. General subjects.

[14]  A. Schutz-Geschwender,et al.  A systematic approach to quantitative Western blot analysis. , 2020, Analytical biochemistry.

[15]  J. A. Visintin,et al.  Exogenous and endogenous factors in seasonality of reproduction in buffalo: A review. , 2020, Theriogenology.

[16]  Kwon-Sik Park,et al.  Recent progress in mapping the emerging landscape of the small-cell lung cancer genome , 2019, Experimental & Molecular Medicine.

[17]  V. Cruzat,et al.  Growth Hormone and Insulin-Like Growth Factor Action in Reproductive Tissues , 2019, Front. Endocrinol..

[18]  M. Alexeyev,et al.  Limited predictive value of TFAM in mitochondrial biogenesis. , 2019, Mitochondrion.

[19]  D. Adhikari,et al.  The spatio-temporal dynamics of mitochondrial membrane potential during oocyte maturation , 2019, Molecular human reproduction.

[20]  Farzane Sivandzade,et al.  Analysis of the Mitochondrial Membrane Potential Using the Cationic JC-1 Dye as a Sensitive Fluorescent Probe. , 2019, Bio-protocol.

[21]  N. Calcutt,et al.  Insulin-like growth factor-1 activates AMPK to augment mitochondrial function and correct neuronal metabolism in sensory neurons in type 1 diabetes , 2018, Molecular metabolism.

[22]  F. Meirelles,et al.  Oocyte mitochondria: role on fertility and disease transmission , 2018, Animal reproduction.

[23]  Samuel Kofi Arhin,et al.  Energy requirements in mammalian oogenesis. , 2018, Cellular and Molecular Biology.

[24]  K. Eliceiri,et al.  GSK3β Regulates Brain Energy Metabolism , 2018, Cell reports.

[25]  Y. Nagao,et al.  Effects of insulin-like growth factor-1 on the in vitro maturation of canine oocytes , 2017, The Journal of reproduction and development.

[26]  A. Schols,et al.  Inactivation of glycogen synthase kinase-3β (GSK-3β) enhances skeletal muscle oxidative metabolism. , 2017, Biochimica et biophysica acta. Molecular basis of disease.

[27]  Yixuan Fan,et al.  Effects of NRF1 on steroidogenesis and apoptosis in goat luteinized granulosa cells. , 2017, Reproduction.

[28]  C. Stocco,et al.  IGF1R Expression in Ovarian Granulosa Cells Is Essential for Steroidogenesis, Follicle Survival, and Fertility in Female Mice , 2017, Endocrinology.

[29]  K. Bremer,et al.  Sensing and responding to energetic stress: The role of the AMPK-PGC1α-NRF1 axis in control of mitochondrial biogenesis in fish. , 2016, Comparative Biochemistry and Physiology Part B Comparative Biochemistry.

[30]  Yong Zhu,et al.  Transcriptomic Signatures for Ovulation in Vertebrates , 2016, bioRxiv.

[31]  M. Shaikh,et al.  Zebrafish: A Versatile Animal Model for Fertility Research , 2016, BioMed research international.

[32]  I. Castilla-Cortázar,et al.  Insulin-like growth factor 1 (IGF-1) therapy: Mitochondrial dysfunction and diseases. , 2016, Biochimica et biophysica acta.

[33]  W. Ge,et al.  Expression and functional characterization of intrafollicular GH-IGF system in the zebrafish ovary. , 2016, General and comparative endocrinology.

[34]  Qi-Li Tang,et al.  Insulin-like growth factor I promotes oocyte maturation through increasing the expression and phosphorylation of epidermal growth factor receptor in the zebrafish ovary , 2016, Molecular and Cellular Endocrinology.

[35]  E. Seli,et al.  Oocyte mitochondrial function and reproduction , 2015, Current opinion in obstetrics & gynecology.

[36]  M. Novin,et al.  The relationship between transcript expression levels of nuclear encoded (TFAM, NRF1) and mitochondrial encoded (MT-CO1) genes in single human oocytes during oocyte maturation , 2015, Balkan journal of medical genetics : BJMG.

[37]  Xiao Sun,et al.  IGFs mediate the action of LH on oocyte maturation in zebrafish. , 2015, Molecular endocrinology.

[38]  M. Nikseresht,et al.  Influence of Insulin-Like Growth Factor-I on Maturation and Fertilization Rate of Immature Oocyte and Embryo Development in NMRI Mouse with TCM199 and α-MEM Medium. , 2014, Journal of clinical and diagnostic research : JCDR.

[39]  C. Oliveira,et al.  Insulin and IGF-1 improve mitochondrial function in a PI-3K/Akt-dependent manner and reduce mitochondrial generation of reactive oxygen species in Huntington's disease knock-in striatal cells. , 2014, Free radical biology & medicine.

[40]  D. Das,et al.  High cAMP attenuation of insulin-stimulated meiotic G2-M1 transition in zebrafish oocytes: Interaction between the cAMP-dependent protein kinase (PKA) and the MAPK3/1 pathways , 2014, Molecular and Cellular Endocrinology.

[41]  Sergey V. Prykhozhij,et al.  Zebrafish as a model system for mitochondrial biology and diseases. , 2014, Translational research : the journal of laboratory and clinical medicine.

[42]  F. Missirlis,et al.  Female and Male Gamete Mitochondria Are Distinct and Complementary in Transcription, Structure, and Genome Function , 2013, Genome biology and evolution.

[43]  D. Das,et al.  Participation of PI3-kinase/Akt signalling in insulin stimulation of p34cdc2 activation in zebrafish oocyte: Phosphodiesterase 3 as a potential downstream target , 2013, Molecular and Cellular Endocrinology.

[44]  Siyu Chen,et al.  Lithium Chloride Inhibits Vascular Smooth Muscle Cell Proliferation and Migration and Alleviates Injury-Induced Neointimal Hyperplasia via Induction of PGC-1α , 2013, PloS one.

[45]  P. Huang,et al.  Follicular development and expression of nuclear respiratory factor-1 and peroxisome proliferator-activated receptor γ coactivator-1 alpha in ovaries of fetal and neonatal doelings. , 2012, Journal of animal science.

[46]  M. Clark,et al.  Zebrafish breeding in the laboratory environment. , 2012, ILAR journal.

[47]  G. J. Van Der Kraak,et al.  Regulation and actions of insulin-like growth factors in the ovary of zebrafish (Danio rerio). , 2012, General and comparative endocrinology.

[48]  J. Rahn,et al.  Bioenergetic Profiling of Zebrafish Embryonic Development , 2011, PloS one.

[49]  A. Sirotkin Growth factors controlling ovarian functions , 2011, Journal of cellular physiology.

[50]  G. J. Van Der Kraak,et al.  Characterization and regulation of the insulin-like growth factor (IGF) system in the zebrafish (Danio rerio) ovary. , 2010, General and comparative endocrinology.

[51]  G. J. Van Der Kraak,et al.  The role of the insulin-like growth factor (IGF) system in zebrafish (Danio rerio) ovarian development. , 2010, General and comparative endocrinology.

[52]  S. Lougheed,et al.  Modular Evolution of PGC-1α in Vertebrates , 2010, Journal of Molecular Evolution.

[53]  R. Dumollard,et al.  Redistribution of Mitochondria Leads to Bursts of ATP Production During Spontaneous Mouse Oocyte Maturation , 2010, Journal of cellular physiology.

[54]  M. Reinecke Insulin-like Growth Factors and Fish Reproduction , 2010, Biology of reproduction.

[55]  D. Hardie,et al.  Calmodulin-dependent protein kinase kinase-β activates AMPK without forming a stable complex: synergistic effects of Ca2+ and AMP , 2009, The Biochemical journal.

[56]  Xiang-yang Zou,et al.  Mitochondrial functions on oocytes and preimplantation embryos , 2009, Journal of Zhejiang University SCIENCE B.

[57]  D. Rawson,et al.  Distributional arrangement of mitochondria in the granulosa cells surrounding stage III zebrafish (Danio rerio) oocytes. , 2009, Theriogenology.

[58]  Johan Auwerx,et al.  PGC-1α, SIRT1 and AMPK, an energy sensing network that controls energy expenditure , 2009, Current opinion in lipidology.

[59]  C. Lessman Oocyte maturation: converting the zebrafish oocyte to the fertilizable egg. , 2009, General and comparative endocrinology.

[60]  Rongfeng Li,et al.  Expression of mitochondrial transcription factor A (TFAM) during porcine gametogenesis and preimplantation embryo development , 2008, Journal of cellular physiology.

[61]  M. Yamashita,et al.  Regulation of oocyte maturation in fish , 2008, Development, growth & differentiation.

[62]  R. Scarpulla Transcriptional paradigms in mammalian mitochondrial biogenesis and function. , 2008, Physiological reviews.

[63]  H. Schatten,et al.  Mitochondrial behavior during oogenesis in zebrafish: A confocal microscopy analysis , 2008, Development, growth & differentiation.

[64]  I. Struewing,et al.  Lithium increases PGC‐1α expression and mitochondrial biogenesis in primary bovine aortic endothelial cells , 2007, The FEBS journal.

[65]  Rongying Tang,et al.  Validation of Zebrafish (Danio rerio) Reference Genes for Quantitative Real-time RT-PCR Normalization , 2007, Acta biochimica et biophysica Sinica.

[66]  P. Lokman,et al.  11-Ketotestosterone and IGF-I increase the size of previtellogenic oocytes from shortfinned eel, Anguilla australis, in vitro. , 2007, Reproduction.

[67]  H. Segner,et al.  Differential expression of IGF-I mRNA and peptide in the male and female gonad during early development of a bony fish, the tilapia Oreochromis niloticus. , 2006, General and comparative endocrinology.

[68]  C. Gustafsson,et al.  Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA , 2002, Nature Genetics.

[69]  S. J. Chan,et al.  Structural, biochemical, and expression analysis of two distinct insulin-like growth factor I receptors and their ligands in zebrafish. , 2002, Endocrinology.

[70]  Jiandie D. Lin,et al.  Peroxisome Proliferator-activated Receptor γ Coactivator 1β (PGC-1β), A Novel PGC-1-related Transcription Coactivator Associated with Host Cell Factor* , 2002, The Journal of Biological Chemistry.

[71]  Thomas D. Schmittgen,et al.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.

[72]  S. Shimasaki,et al.  The physiology of folliculogenesis: the role of novel growth factors. , 2001, Fertility and sterility.

[73]  C. Bondy,et al.  Granulosa cell proliferation is impaired in the Igf1 null ovary. , 2001, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

[74]  P Barrière,et al.  Mitochondrial DNA content affects the fertilizability of human oocytes. , 2001, Molecular human reproduction.

[75]  R. Jansen Germline passage of mitochondria: quantitative considerations and possible embryological sequelae. , 2000, Human reproduction.

[76]  H. Habibi,et al.  Direct action of GnRH variants on goldfish oocyte meiosis and follicular steroidogenesis , 2000, Molecular and Cellular Endocrinology.

[77]  R. Patiño,et al.  Regulation of gap junctions and oocyte maturational competence by gonadotropin and insulin-like growth factor-I in ovarian follicles of red seabream. , 1999, General and comparative endocrinology.

[78]  R. Wallace,et al.  Effects of insulin-like growth factor-I on final oocyte maturation and steroid production in Fundulus heteroclitus , 1998, Fish Physiology and Biochemistry.

[79]  M. Illera,et al.  Enhancement of cumulus expansion and nuclear maturation during bovine oocyte maturation in vitro by the addition of epidermal growth factor and insulin-like growth factor I. , 1994, Journal of reproduction and fertility.

[80]  K. Aida,et al.  Insulin and insulin-like growth factors I and II induce final maturation of oocytes of red seabream, Pagrus major, in vitro. , 1994, General and comparative endocrinology.

[81]  O. H. Lowry,et al.  The explanation for the blockade of glycolysis in early mouse embryos. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[82]  OUP accepted manuscript , 2022, Human Reproduction.

[83]  U. Mukherjee,et al.  Hormonally Active Agents: A Menace for Oogenesis and Fertility in Teleosts , 2021 .

[84]  D. Das,et al.  Releasing prophase arrest in zebrafish oocyte: synergism between maturational steroid and Igf1. , 2016, Reproduction.

[85]  Aritro Sen,et al.  Oocyte maturation: a story of arrest and release. , 2013, Frontiers in bioscience.

[86]  E. Verdin,et al.  Mitochondrial sirtuins. , 2010, Biochimica et biophysica acta.

[87]  E. Adashi,et al.  The Role of Growth Factors in Ovarian Function and Development , 2009 .

[88]  BMC Molecular Biology BioMed Central Research article Interaction of circadian clock proteins PER2 and CRY with BMAL1 and CLOCK , 2008 .

[89]  Thomas Braunbeck,et al.  Towards an alternative for the acute fish LC(50) test in chemical assessment: the fish embryo toxicity test goes multi-species -- an update. , 2005, ALTEX.

[90]  Jiandie D. Lin,et al.  Peroxisome proliferator-activated receptor gamma coactivator 1beta (PGC-1beta ), a novel PGC-1-related transcription coactivator associated with host cell factor. , 2002, The Journal of biological chemistry.

[91]  R. Kaul,et al.  Insulin like growth factor 1 and regulation of ovarian function in mammals. , 2002, Indian journal of experimental biology.

[92]  R. Nagel DarT: The embryo test with the Zebrafish Danio rerio--a general model in ecotoxicology and toxicology. , 2002, ALTEX.

[93]  P. Thomas,et al.  Upregulation of the Maturation-Inducing Steroid Membrane Receptor in Spotted Seatrout Ovaries by Gonadotropin During Oocyte Maturation and Its Physiological Significance1 , 2001, Biology of reproduction.

[94]  M. Westerfield The zebrafish book : a guide for the laboratory use of zebrafish (Danio rerio) , 1995 .

[95]  G. Chieffi Control of reproductive cycles in metazoa: Exogenous and endogenous factors , 1984 .