Neurotrophin-4 promotes the specification of trophectoderm lineage after parthenogenetic activation and enhances porcine early embryonic development

Neurotrophin-4 (NT-4), a neurotrophic factor, appears to affect early embryonic development because it is secreted not only by neurons but also by oviductal and uterine epithelial cells. However, no studies have characterized the effects of NT-4 on early embryonic development in pigs. In this study, we applied the experimental model of parthenogenetic-activation (PA)-derived embryos. Herein, we investigated the effect of NT-4 supplementation during the in vitro culture (IVC) of embryos, analyzed the transcription levels of specific genes, and outlined the first cell lineage specification for porcine PA-derived blastocysts. We confirmed that NT-4 and its receptor proteins were localized in both the inner cell mass (ICM) and trophectoderm (TE) in porcine blastocysts. Across different concentrations (0, 1, 10, and 100 ng/mL) of NT-4 supplementation, the optimal concentration of NT-4 to improve the developmental competence of porcine parthenotes was 10 ng/mL. NT-4 supplementation during porcine IVC significantly (p < 0.05) increased the proportion of TE cells by inducing the transcription of TE lineage markers (CDX2, PPAG3, and GATA3 transcripts). NT-4 also reduced blastocyst apoptosis by regulating the transcription of apoptosis-related genes (BAX and BCL2L1 transcripts) and improved blastocyst quality via the interaction of neurotrophin-, Hippo-yes-associated protein (Hippo-YAP) and mitogen-activated protein kinase/extracellular regulated kinase (MAPK/ERK) pathway. Additionally, NT-4 supplementation during IVC significantly (p < 0.05) increased YAP1 transcript levels and significantly (p < 0.01) decreased LATS2 transcript levels, respectively, in the porcine PA-derived blastocysts. We also confirmed through fluorescence intensity that the YAP1 protein was significantly (p < 0.001) increased in the NT-4-treated blastocysts compared with that in the control. NT-4 also promoted differentiation into the TE lineage rather than into the ICM lineage during porcine early embryonic development. In conclusion, 10 ng/mL NT-4 supplementation enhanced blastocyst quality by regulating the apoptosis- and TE lineage specification-related genes and interacting with neurotrophin-, Hippo-YAP-, and MAPK/ERK signaling pathway during porcine in vitro embryo development.

[1]  P. Pawlak,et al.  Species and embryo genome origin affect lipid droplets in preimplantation embryos , 2023, Frontiers in Cell and Developmental Biology.

[2]  Yan-zhong Chang,et al.  The emerging role of furin in neurodegenerative and neuropsychiatric diseases , 2022, Translational Neurodegeneration.

[3]  S. Hyun,et al.  Physiological and Functional Roles of Neurotrophin-4 During In Vitro Maturation of Porcine Cumulus–Oocyte Complexes , 2022, Frontiers in Cell and Developmental Biology.

[4]  Ran Zhang,et al.  Generation and characterization of stable pig pregastrulation epiblast stem cell lines , 2021, Cell Research.

[5]  S. Hyun,et al.  Beneficial Effects of Neurotrophin-4 Supplementation During in vitro Maturation of Porcine Cumulus-Oocyte Complexes and Subsequent Embryonic Development After Parthenogenetic Activation , 2021, Frontiers in Veterinary Science.

[6]  L. Spate,et al.  Challenges and Considerations during In Vitro Production of Porcine Embryos , 2021, Cells.

[7]  Jiana Huang,et al.  Single-cell transcriptome and cell-specific network analysis reveal the reparative effect of neurotrophin-4 in preantral follicles grown in vitro , 2021, Reproductive Biology and Endocrinology.

[8]  L. Spate,et al.  Effects of RAD51-stimulatory compound 1 (RS-1) and its vehicle, DMSO, on pig embryo culture. , 2021, Reproductive Toxicology.

[9]  F. Gandolfi,et al.  Generation of Trophoblast-Like Cells From Hypomethylated Porcine Adult Dermal Fibroblasts , 2021, Frontiers in Veterinary Science.

[10]  Chang-Kyu Lee,et al.  SOX2 plays a crucial role in cell proliferation and lineage segregation during porcine pre‐implantation embryo development , 2021, Cell proliferation.

[11]  T. Dawson,et al.  Protocol for measurement of calcium dysregulation in human induced pluripotent stem cell-derived dopaminergic neurons , 2021, STAR Protocols.

[12]  M. Kurome,et al.  Transcriptome dynamics in early in vivo developing and in vitro produced porcine embryos , 2021, BMC Genomics.

[13]  K. Sawai,et al.  Effect of Downregulating the Hippo Pathway Members YAP1 and LATS2 Transcripts on Early Development and Gene Expression Involved in Differentiation in Porcine Embryos. , 2020, Cellular reprogramming.

[14]  R. Bevacqua,et al.  DMSO supplementation during in vitro maturation of bovine oocytes improves blastocyst rate and quality. , 2020, Theriogenology.

[15]  M. Fiore,et al.  Role of neurotrophins in pregnancy, delivery and postpartum. , 2020, European journal of obstetrics, gynecology, and reproductive biology.

[16]  Yunhai Zhang,et al.  Maternal Yes-Associated Protein Participates in Porcine Blastocyst Development via Modulation of Trophectoderm Epithelium Barrier Function , 2019, Cells.

[17]  H. Iwata,et al.  Establishment of human trophoblast stem cells from human induced pluripotent stem cell-derived cystic cells under micromesh culture , 2019, Stem Cell Research & Therapy.

[18]  S. Hyun,et al.  Growth differentiation factor 8 regulates SMAD2/3 signaling and improves oocyte quality during porcine oocyte maturation in vitro † , 2019, Biology of Reproduction.

[19]  S. Hyun,et al.  GDF8 enhances SOX2 expression and blastocyst total cell number in porcine IVF embryo development. , 2019, Theriogenology.

[20]  Xu Zhou,et al.  Brain‐derived neurotrophic factor promotes proliferation and progesterone synthesis in bovine granulosa cells , 2018, Journal of cellular physiology.

[21]  M. Manzanares,et al.  Transitions in cell potency during early mouse development are driven by Notch , 2018, bioRxiv.

[22]  F. Bazer,et al.  Brain‐derived neurotrophic factor improves proliferation of endometrial epithelial cells by inhibition of endoplasmic reticulum stress during early pregnancy , 2017, Journal of cellular physiology.

[23]  K. Miyasaka,et al.  Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm , 2017, Scientific Reports.

[24]  Gerelchimeg Bou,et al.  CDX2 is essential for cell proliferation and polarity in porcine blastocysts , 2017, Development.

[25]  H. Sasaki Roles and regulations of Hippo signaling during preimplantation mouse development , 2017, Development, growth & differentiation.

[26]  Valeria Levi,et al.  Long-Lived Binding of Sox2 to DNA Predicts Cell Fate in the Four-Cell Mouse Embryo , 2016, Cell.

[27]  C. Lorthongpanich,et al.  Emerging Role of the Hippo Signaling Pathway in Position Sensing and Lineage Specification in Mammalian Preimplantation Embryos1 , 2015, Biology of reproduction.

[28]  A. Cooney,et al.  Sox2 is the faithful marker for pluripotency in pig: Evidence from embryonic studies , 2015, Developmental dynamics : an official publication of the American Association of Anatomists.

[29]  Richard A. Lang,et al.  HIPPO Pathway Members Restrict SOX2 to the Inner Cell Mass Where It Promotes ICM Fates in the Mouse Blastocyst , 2014, PLoS genetics.

[30]  M. Dhobale Neurotrophins: Role in adverse pregnancy outcome , 2014, International Journal of Developmental Neuroscience.

[31]  Miguel Manzanares,et al.  Notch and hippo converge on Cdx2 to specify the trophectoderm lineage in the mouse blastocyst. , 2014, Developmental cell.

[32]  Kazuhiro Chida,et al.  Polarity-Dependent Distribution of Angiomotin Localizes Hippo Signaling in Preimplantation Embryos , 2013, Current Biology.

[33]  D. Solter,et al.  Temporal reduction of LATS kinases in the early preimplantation embryo prevents ICM lineage differentiation. , 2013, Genes & development.

[34]  Tristan Frum,et al.  Oct4 cell-autonomously promotes primitive endoderm development in the mouse blastocyst. , 2013, Developmental cell.

[35]  K. Sawai,et al.  Changes in the Expression Patterns of the Genes Involved in the Segregation and Function of Inner Cell Mass and Trophectoderm Lineages During Porcine Preimplantation Development , 2012, The Journal of reproduction and development.

[36]  F. Strejček,et al.  Early aberrations in chromatin dynamics in embryos produced under in vitro conditions. , 2012, Cellular reprogramming.

[37]  Lan-rong Zheng,et al.  [Morphological study on development of nerve growth factor-positive neurons in the cerebellum of human fetus]. , 2012, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae.

[38]  M. Kaczmarek,et al.  Mechanisms for the establishment of pregnancy in the pig. , 2011, Reproduction in domestic animals = Zuchthygiene.

[39]  K. Sawai,et al.  Aberrant expression patterns of genes involved in segregation of inner cell mass and trophectoderm lineages in bovine embryos derived from somatic cell nuclear transfer. , 2010, Cellular reprogramming.

[40]  C Junien,et al.  Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and human. , 2010, Placenta.

[41]  Mikael Huss,et al.  Resolution of cell fate decisions revealed by single-cell gene expression analysis from zygote to blastocyst. , 2010, Developmental cell.

[42]  H. Wang,et al.  The proprotein convertase furin in human trophoblast: Possible role in promoting trophoblast cell migration and invasion. , 2009, Placenta.

[43]  Soumen Paul,et al.  GATA3 Is Selectively Expressed in the Trophectoderm of Peri-implantation Embryo and Directly Regulates Cdx2 Gene Expression* , 2009, The Journal of Biological Chemistry.

[44]  J. Kumagai,et al.  Brain-derived neurotrophic factor promotes implantation and subsequent placental development by stimulating trophoblast cell growth and survival. , 2009, Endocrinology.

[45]  M. Muñoz,et al.  Tyrosine kinase A, C and fibroblast growth factor-2 receptors in bovine embryos cultured in vitro. , 2009, Theriogenology.

[46]  P. Toti,et al.  Expression of Placental Neurotrophin-3 (NT-3) in Physiological Pregnancy, Preeclampsia and Chorioamnionitis , 2009, Clinical medicine. Pathology.

[47]  X. Zhou,et al.  The mRNA expression of brain-derived neurotrophic factor in oocytes and embryos and its effects on the development of early embryos in cattle. , 2008, Animal : an international journal of animal bioscience.

[48]  Guoji Guo,et al.  Role of Cdx2 and cell polarity in cell allocation and specification of trophectoderm and inner cell mass in the mouse embryo. , 2008, Genes & development.

[49]  A. Gutiérrez-Adán,et al.  Consequences of in vitro culture conditions on embryo development and quality. , 2008, Reproduction in domestic animals = Zuchthygiene.

[50]  G. Ragni,et al.  Parthenogenetic activation: biology and applications in the ART laboratory. , 2008, Placenta.

[51]  Jiandie D. Lin,et al.  TEAD mediates YAP-dependent gene induction and growth control. , 2008, Genes & development.

[52]  K. Richter,et al.  The importance of growth factors for preimplantation embryo development and in-vitro culture , 2008, Current opinion in obstetrics & gynecology.

[53]  B. Roelen,et al.  Differences in early lineage segregation between mammals , 2008, Developmental dynamics : an official publication of the American Association of Anatomists.

[54]  R. Roberts,et al.  Human embryonic stem cells as models for trophoblast differentiation. , 2008, Placenta.

[55]  Shinji Yamamoto,et al.  Tead4 is required for specification of trophectoderm in pre-implantation mouse embryos , 2008, Mechanisms of Development.

[56]  E. Crivellato,et al.  Nerve growth factor as an angiogenic factor. , 2008, Microvascular research.

[57]  A. Hsueh,et al.  Regulation of preimplantation embryo development by brain-derived neurotrophic factor. , 2007, Developmental biology.

[58]  Ian G. Mills,et al.  The developing role of receptors and adaptors , 2006, Nature Reviews Cancer.

[59]  F. Petraglia,et al.  Human placenta and fetal membranes express nerve growth factor mRNA and protein , 2006, Journal of endocrinological investigation.

[60]  J. Krolewski Cytokine and growth factor receptors in the nucleus: What's up with that? , 2005, Journal of cellular biochemistry.

[61]  Janet Rossant,et al.  Cdx2 is required for correct cell fate specification and differentiation of trophectoderm in the mouse blastocyst , 2005, Development.

[62]  K. Red-Horse,et al.  Trophoblast differentiation during embryo implantation and formation of the maternal-fetal interface. , 2004, The Journal of clinical investigation.

[63]  B. Hempstead,et al.  Paracrine and Autocrine Functions of Brain-derived Neurotrophic Factor (BDNF) and Nerve Growth Factor (NGF) in Brain-derived Endothelial Cells* , 2004, Journal of Biological Chemistry.

[64]  Jeff Reese,et al.  Molecular cues to implantation. , 2004, Endocrine reviews.

[65]  Wendy Dean,et al.  Epigenetic asymmetry in the mammalian zygote and early embryo: relationship to lineage commitment? , 2003, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[66]  N. Seidah,et al.  The secretory proprotein convertases furin, PC5, and PC7 activate VEGF-C to induce tumorigenesis. , 2003, The Journal of clinical investigation.

[67]  G. Carpenter Nuclear localization and possible functions of receptor tyrosine kinases. , 2003, Current opinion in cell biology.

[68]  C. Dreyfus,et al.  Neurotrophin-4/5 and neurotrophin-3 are present within the human ovarian follicle but appear to have different paracrine/autocrine functions. , 2002, The Journal of clinical endocrinology and metabolism.

[69]  Michael Karin,et al.  NF-κB at the crossroads of life and death , 2002, Nature Immunology.

[70]  K. Hardy,et al.  Growth factor expression and function in the human and mouse preimplantation embryo. , 2002, The Journal of endocrinology.

[71]  A. Patapoutian,et al.  Trk receptors: mediators of neurotrophin action , 2001, Current Opinion in Neurobiology.

[72]  Y. Barde,et al.  Neurotrophins: key regulators of cell fate and cell shape in the vertebrate nervous system. , 2000, Genes & development.

[73]  David R Kaplan,et al.  Neurotrophin signal transduction in the nervous system , 2000, Current Opinion in Neurobiology.

[74]  H. Schöler,et al.  Formation of Pluripotent Stem Cells in the Mammalian Embryo Depends on the POU Transcription Factor Oct4 , 1998, Cell.

[75]  R. Schultz,et al.  Increased Incidence of Apoptosis in Transforming Growth Factor α-Deficient Mouse Blastocysts , 1998 .

[76]  Y. Kanai,et al.  Nerve growth factor promotes giant-cell transformation of mouse trophoblast cells in vitro. , 1997, Biochemical and biophysical research communications.

[77]  Lawrence C. Katz,et al.  Neurotrophins regulate dendritic growth in developing visual cortex , 1995, Neuron.

[78]  D. Steiner,et al.  Mutational Analysis of the Insulin-like Growth Factor I Prohormone Processing Site (*) , 1995, The Journal of Biological Chemistry.

[79]  H. Schöler,et al.  Oct-4 transcription factor is differentially expressed in the mouse embryo during establishment of the first two extraembryonic cell lineages involved in implantation. , 1994, Developmental biology.

[80]  K. Okuda,et al.  In-vitro penetration of pig oocytes matured in culture by frozen-thawed ejaculated spermatozoa. , 1991, Journal of reproduction and fertility.

[81]  M. Dhobale Neurotrophic Factors and Maternal Nutrition During Pregnancy. , 2017, Vitamins and hormones.

[82]  S. Joshi,et al.  Neurotrophins: Role in Placental Growth and Development. , 2017, Vitamins and hormones.

[83]  M. Hung,et al.  Receptor Tyrosine Kinases in the Nucleus: Nuclear Functions and Therapeutic Implications in Cancers , 2014 .

[84]  P. Pfeffer,et al.  Trophoblast development. , 2012, Reproduction.

[85]  L. R. Abeydeera In vitro production of embryos in swine. , 2002, Theriogenology.