Cannabinoid receptor type 1 regulates sequential stages of migration and morphogenesis of neural crest cells and derivatives in chicken and frog embryos

The main cannabinoid receptor CB1R first shows expression during early neurula stage in chicken (Gallus gallus) embryos, and at early tailbud stage in the frog (Xenopus laevis) embryos. This raises the question of whether CB1R regulates similar or distinct processes during the embryonic development of these two species. Here, we examined whether CB1R influences the migration and morphogenesis of neural crest cells and derivatives in both chicken and frog embryos. Early neurula stage chicken embryos were exposed to arachidonyl‐2ʹ‐chloroethylamide (ACEA; a CB1R agonist), N‐(Piperidin‐1‐yl)‐5‐(4‐iodophenyl)‐1‐(2,4‐dichlorophenyl)‐4‐methyl‐1H‐pyrazole‐3‐carboxamide (AM251; a CB1R inverse agonist) or Blebbistatin (nonmuscle Myosin II inhibitor) in ovo and examined during migration of neural crest cells and at condensing cranial ganglia stage. Early tailbud stage frog embryos were bathed in ACEA, AM251 or Blebbistatin, and analyzed at late tailbud stage for changes in craniofacial and eye morphogenesis, and in patterning and morphology of melanophores (neural crest‐derived pigment cells). In chicken embryos exposed to ACEA and Myosin II inhibitor, cranial neural crest cells migrated erratically from the neural tube, and the right, but not the left, ophthalmic nerve of the trigeminal ganglia was affected in ACEA‐ and AM251‐treated embryos. In frog embryos with inactivation or activation of CB1R, or inhibition of Myosin II, the craniofacial and eye regions were smaller and/or less developed, and the melanophores overlying the posterior midbrain were more dense, and stellate in morphology, than the same tissues and cells in control embryos. This data suggests that despite differences in the time of onset of expression, normal activity of CB1R is required for sequential steps in migration and morphogenesis of neural crest cells and derivatives in both chicken and frog embryos. In addition, CB1R may signal through Myosin II to regulate migration and morphogenesis of neural crest cells and derivatives in chicken and frog embryos.

[1]  T. Elul,et al.  Cannabinoid Receptor Type 1 regulates growth cone filopodia and axon dispersion in the optic tract of Xenopus laevis tadpoles , 2022, The European journal of neuroscience.

[2]  S. Hayat,et al.  Phytocannabinoids Biosynthesis in Angiosperms, Fungi, and Liverworts and Their Versatile Role , 2021, Plants.

[3]  P. Rakic,et al.  Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration , 2020, International journal of molecular sciences.

[4]  B. Møller,et al.  Phytocannabinoids: Origins and Biosynthesis. , 2020, Trends in plant science.

[5]  R. Or,et al.  Cannabis, the Endocannabinoid System and Immunity—the Journey from the Bedside to the Bench and Back , 2020, International journal of molecular sciences.

[6]  ByTETSUO Takeichi,et al.  Xenopus laevis , 2008 .

[7]  B. Jones,et al.  Optic cup morphogenesis requires neural crest-mediated basement membrane assembly , 2020, Development.

[8]  Robert J. Silver The Endocannabinoid System of Animals , 2019, Animals : an open access journal from MDPI.

[9]  C. K. Thompson,et al.  “The flavor enhancer maltol increases pigment aggregation in dermal and neural melanophores in Xenopus laevis tadpoles” , 2019, bioRxiv.

[10]  F. Dehghani,et al.  On the influence of cannabinoids on cell morphology and motility of glioblastoma cells , 2019, PloS one.

[11]  L. Taneyhill,et al.  Cadherin‐7 mediates proper neural crest cell–placodal neuron interactions during trigeminal ganglion assembly , 2019, Genesis.

[12]  K. Willett,et al.  Developmental Effects of Cannabidiol and &Dgr;9-Tetrahydrocannabinol in Zebrafish , 2018, Toxicological sciences : an official journal of the Society of Toxicology.

[13]  P. Thiébaud,et al.  Vestigial-like 3 is a novel Ets1 interacting partner and regulates trigeminal nerve formation and cranial neural crest migration , 2017, Biology Open.

[14]  Su Guo,et al.  Role of the endocannabinoid system in vertebrates: Emphasis on the zebrafish model , 2017, Development, growth & differentiation.

[15]  B. Budzyńska,et al.  Endocannabinoid System: the Direct and Indirect Involvement in the Memory and Learning Processes—a Short Review , 2016, Molecular Neurobiology.

[16]  L. K. Baker,et al.  Dose-dependent teratogenicity of the synthetic cannabinoid CP-55,940 in mice. , 2016, Neurotoxicology and teratology.

[17]  E. Nishida,et al.  cnrip1 is a regulator of eye and neural development in Xenopus laevis , 2015, Genes to cells : devoted to molecular & cellular mechanisms.

[18]  F. Rico,et al.  Cannabinoid-induced actomyosin contractility shapes neuronal morphology and growth , 2014, eLife.

[19]  M. Ko,et al.  Silencing or Amplification of Endocannabinoid Signaling in Blastocysts via CB1 Compromises Trophoblast Cell Migration* , 2012, The Journal of Biological Chemistry.

[20]  T. Cooper,et al.  Cannabinoid receptor 1 signaling in embryo neurodevelopment. , 2012, Birth defects research. Part B, Developmental and reproductive toxicology.

[21]  J. Lanciego,et al.  Cannabinoid receptors CB 1 and CB 2 form functional heteromers in the brain # , 2012 .

[22]  R. McLennan,et al.  Cranial neural crest migration: new rules for an old road. , 2010, Developmental biology.

[23]  C. Bass,et al.  Synthetic cannabinoid receptor agonists inhibit tumor growth and metastasis of breast cancer , 2009, Molecular Cancer Therapeutics.

[24]  S. Bell,et al.  Reproductive Biology and Endocrinology Spatio-temporal Expression Patterns of Anandamide-binding Receptors in Rat Implantation Sites: Evidence for a Role of the Endocannabinoid System during the Period of Placental Development , 1987 .

[25]  M. Bronner‐Fraser,et al.  Birth of ophthalmic trigeminal neurons initiates early in the placodal ectoderm , 2009, The Journal of comparative neurology.

[26]  Tobias Langenberg,et al.  Rho-kinase and myosin II affect dynamic neural crest cell behaviors during epithelial to mesenchymal transition in vivo. , 2008, Developmental biology.

[27]  T. Cooper,et al.  A cannabinoid analogue of Delta9-tetrahydrocannabinol disrupts neural development in chick. , 2008, Birth defects research. Part B, Developmental and reproductive toxicology.

[28]  A. Graham,et al.  The endocannabinoid receptor, CB1, is required for normal axonal growth and fasciculation , 2008, Molecular and Cellular Neuroscience.

[29]  Raman M. Das,et al.  Robo2-Slit1 dependent cell-cell interactions mediate assembly of the trigeminal ganglion , 2008, Nature Neuroscience.

[30]  S. Bell,et al.  The role of the endocannabinoid system in gametogenesis, implantation and early pregnancy. , 2007, Human reproduction update.

[31]  Michela Matteoli,et al.  Hardwiring the Brain: Endocannabinoids Shape Neuronal Connectivity , 2007, Science.

[32]  D. Schild,et al.  Cannabinoid action in the olfactory epithelium , 2007, Proceedings of the National Academy of Sciences.

[33]  M. Bronner‐Fraser,et al.  Neuropilin 2/semaphorin 3F signaling is essential for cranial neural crest migration and trigeminal ganglion condensation , 2007, Developmental neurobiology.

[34]  M. Glass,et al.  Evolutionary origins of the endocannabinoid system. , 2006, Gene.

[35]  P. Trainor Specification and Patterning of Neural Crest Cells During Craniofacial Development , 2005, Brain, Behavior and Evolution.

[36]  K. Mackie Cannabinoid receptor homo- and heterodimerization. , 2005, Life sciences.

[37]  Timothy J Mitchison,et al.  Dissecting Temporal and Spatial Control of Cytokinesis with a Myosin II Inhibitor , 2003, Science.

[38]  S. Yazulla,et al.  Biphasic modulation of voltage-dependent currents of retinal cones by cannabinoid CB1 receptor agonist WIN 55212-2 , 2003, Visual Neuroscience.

[39]  S. Fraser,et al.  Neural crest cell dynamics revealed by time-lapse video microscopy of whole embryo chick explant cultures. , 1998, Developmental biology.

[40]  C. Holt,et al.  Navigational errors made by growth cones without filopodia in the embryonic xenopus brain , 1993, Neuron.

[41]  B. Martin,et al.  Plasma concentrations of delta-9-tetrahydrocannabinol in dams and fetuses following acute or multiple prenatal dosing in rats. , 1989, Life sciences.

[42]  N. L. Le Douarin,et al.  Development of the peripheral nervous system from the neural crest. , 1988, Annual review of cell biology.

[43]  W. Slikker,et al.  Fetal disposition of delta 9-tetrahydrocannabinol (THC) during late pregnancy in the rhesus monkey. , 1987, Toxicology and applied pharmacology.

[44]  G. Morrill,et al.  The effect of intragastric administration of delta 9-tetrahydrocannabinol on the growth and development of fetal mice of the A/J strain. , 1986, Toxicology and applied pharmacology.

[45]  T. Persaud,et al.  Teratogenic activity of cannabis resin. , 1968, Lancet.

[46]  Viktor Hamburger,et al.  A series of normal stages in the development of the chick embryo , 1992, Journal of morphology.