Forskolin Effect on the Lineage Specification of Trunk Neural Crest Cells in vitro

  • Jin, Eun-Jung (Section of Molecular and Cellular Biology, The University of California)
  • Published : 2002.03.01

Abstract

Recent evidence has suggested that trunk neural crest cell generally assumed to have equivalent differentiation potentials, demonstrate differentiation bias along the anterior/posterior axis. In amphibian and fish, neural crest cells give rise to three chromatophore types, melanophores, xantho-phores, and iridophores. Each pigment cell type has distinct characteristics but there is speculation about the cellular plasticity that exists among them. Neural crest cells migrate along specific routes, ventromedially and dorsolaterally. Neural crest cells that travel dorsolaterally are the first cells to begin migration in the axolotl and are the major contributors to the visible pigment pattern. Many factors and mechanisms that are responsible for guiding migratory neural crest cells along potential pathways or determining their fate remain unknown. A single lineage of the crest, which becomes restricted to one of the three pigment cell types, gives us the opportunity to examine the existence of neural crest stem cell populations and cellular plasticity. Study presented here showed results from recent in vitro studies designed to identify parameters influencing differentiation events of individual neural crest-derived pigment cell lineages. Melanophore production from neural crest explants originating from different levels along the anterior/posterior axis of wild type-axolotl embryos were compared and demonstrate that the differentiation of melanophores is enhanced in subpopulation of neural crest treated with forskolin. Forskolin (an adenylate cyclase activator) increases intracellular CAMP concentration and eventually activates the protein kinase-A signaling pathway. Melanophore number, melanin content, and tyrosinase activity in explants taken from the anterior-most region of the crest increased significantly in response to forskolin treatment. This study suggests implications of region specific influences and developmental regulation in the development of pigment pattern.

Keywords

References

  1. Artinger KB and Bronner-Fraser M (1992) Notochord grafts do not suppress formation of neural crest cells or commissural neurons. Development 116: 877-886
  2. Bordzilvskaya VI and Detlaff TA (1979) Table of stages of the normal development of axolotl embryos and the prognostication of timing successive development stages at various temperatures. Axolotl Newsl 7: 2-22
  3. Frost SK and Bagnara JT (1979) Allopurinol-induced melanism in the tiger salamander (Ambystoma tigtinum nebuosum). J Exp Zool 209: 455-466 https://doi.org/10.1002/jez.1402090311
  4. Frost SK, Robinson SJ, Carson MK, Thorsteinsdottir S, and Giesler J (1987) The effects of exogenous guanosine on chromatophore differentiation in the axolotl. Pigment Cell Res 1: 37-43 https://doi.org/10.1111/j.1600-0749.1987.tb00532.x
  5. Frost SK, Briggs F, and Malacinski GM (1984a) A color atlas of pigment genes in the Mexican axolotl (AmbystomaMexicanum). Differentiation 26: 182-188 https://doi.org/10.1111/j.1432-0436.1984.tb01393.x
  6. Frost SK, Epp LG, and Robinson SJ (1984b) The pigmentary system of developing axolotls: A biochemical and structural analysis of chromatophores in wild type axolotls. J Embryol Exp Morphol 81: 105-125
  7. Frost SK (1988) Factors that control chromatophore differentiation in vivo. In: Bagnara JT (ed) Advances in Pigment Cell Research. Alan R. Liss, New York. pp 23-24
  8. Ghysen A, Dambly-Chaudiere C, Jan LY, and Jan YN (1993) Cell interaction and gene interaction in peripheral neurogenesis. Genes Dev 7: 723-733 https://doi.org/10.1101/gad.7.5.723
  9. Henion PD and Weston JA (1997) Timing and pattern of cell fate restrictions in the neural crest lineage. Development 124: 4351-4359
  10. Ide H (1973) Effects of ACTH on melanophores and iridophores isolated from bullfrog tadpoles. Gen Comp Endocrinol 21: 390-397 https://doi.org/10.1016/0016-6480(73)90072-5
  11. Ide H (1974) Further studies on the hormonal control of melanophores and iridophores isolated from bullfrog tadpoles. Gen Comp Endocrinol 24: 341-345 https://doi.org/10.1016/0016-6480(74)90189-0
  12. Jin EJ and Thibaudeau G (1999) Effects of lithium on pigmentation in the embryonic zebrafish (Brachydanio rerio). Biochim Biophys Acta 1449: 93-99 https://doi.org/10.1016/S0167-4889(98)00176-1
  13. Kajishima T (1958) Regional differentces in pigment cell fomation of the embryonic shield of the goldfish. Embryologia 4: 133-147 https://doi.org/10.1111/j.1440-169X.1958.tb00151.x
  14. Kondo H and Ide H (1983) Long-term cultivation of amphibian melanophores. In vitro ageing and spontaneous transformation to a continuous cell line. Exp Cell Res 149: 247-256 https://doi.org/10.1016/0014-4827(83)90396-8
  15. Le Douarin NM, Dupin E, and Ziller C (1994) Genetic and epigenetic control in neural crest development. Curr Opin Genet Dev 4: 685-695 https://doi.org/10.1016/0959-437X(94)90135-P
  16. Morrison-Graham K and Weston JA (1993) Transient steel factor dependence by neural crest-derived melanocyte precursors. Dev Biol 159: 346-352 https://doi.org/10.1006/dbio.1993.1246
  17. Nakagawa Y, Kaneko T, Ogura T, Suzuke T, Torii M, and Kaibuchi K (1996) Roles of cell-autonomous mechanisms for differential expression of region-specific transcription factors in neuroepithelial cells. Development 122: 2449-2464
  18. Nicolas JF, Mathis L, Bonnerot C, and Saurin W (1996) Evidence in the mouse for self-renewing stem cells in the formation of a segmented longitudinal structure, the myotome. Development 122: 2933-2946
  19. Raible DW and Eisen JS (1994) Restriction of neural crest cell fate in the trunk of the embryonic zebrafish. Development 120: 495-503
  20. Reedy MV, Faraco CD, and Erickson CA (1998) Specification and migration of melanoblasts at the vagal level and in hyperpigmented Silkie chickens. Dev Dyn 213: 476-485 https://doi.org/10.1002/(SICI)1097-0177(199812)213:4<476::AID-AJA12>3.0.CO;2-R
  21. Stemple DL and Anderson DJ (1992) Isolation of a stem cell for neurons and glial from the mammalian neural crest. Cell 71: 973-985 https://doi.org/10.1016/0092-8674(92)90393-Q
  22. Thibaudeau G, Holder S, and Patrick G (1999) Anterior/posterior influences on neural crest-derived pigment cell differentiation. Pigment Cell Res 11: 189-197 https://doi.org/10.1111/j.1600-0749.1998.tb00729.x
  23. Thibaudeau G and Frost-Mason SK (1992) Inhibition of neural crest cell differentiation by embryo ectodermal extract. J Exp Zool 261: 431-440 https://doi.org/10.1002/jez.1402610410
  24. Yamada T, Pfaff SL, Edlund T, and Jessell TM (1993) Control of cell pattern in the neural tube: motor neuron induction by diffusible factors from notochord and floor plate. Cell 73: 673-686 https://doi.org/10.1016/0092-8674(93)90248-O
  25. Yoshida H, Kunisada T, Kusakabe M, Nishikawa S, and Nishikawa SI (1996) Distinct stages of melanocyte differentiation revealed by anlaysis of nonuniform pigmentation patterns. Development 122: 1207-1214