Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1995 Jul 18;92(15):6952–6956. doi: 10.1073/pnas.92.15.6952

Activin A inhibits Pax-6 expression and perturbs cell differentiation in the developing spinal cord in vitro.

F Pituello 1, G Yamada 1, P Gruss 1
PMCID: PMC41449  PMID: 7624351

Abstract

We have developed an in vitro model of the isolated chicken neural plate. Here we demonstrate that even in the absence of notochord, the neural plate rapidly develops a typical dorsoventral patterning. This observation suggests that the ventral cell types are specified or at least predetermined prior to notochord formation and that permissive conditions are sufficient for differentiation of ventral structures. Treatment of the neural plate with activin A extinguishes Pax-6 gene expression, whereas the dorsal markers Pax-3 and Pax-7 are still expressed. The absence of Pax-6 transcripts can be correlated with an impeded differentiation of the motor neurons, whereas the floor plate seems to be enlarged. We propose that the region-specific expression of Pax-6 in the spinal cord is under the control of activin-like molecules.

Full text

PDF
6952

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alvarez I. S., Schoenwolf G. C. Patterns of neurepithelial cell rearrangement during avian neurulation are determined prior to notochordal inductive interactions. Dev Biol. 1991 Jan;143(1):78–92. doi: 10.1016/0012-1606(91)90056-9. [DOI] [PubMed] [Google Scholar]
  2. Ang S. L., Rossant J. HNF-3 beta is essential for node and notochord formation in mouse development. Cell. 1994 Aug 26;78(4):561–574. doi: 10.1016/0092-8674(94)90522-3. [DOI] [PubMed] [Google Scholar]
  3. Artinger K. B., Bronner-Fraser M. Delayed formation of the floor plate after ablation of the avian notochord. Neuron. 1993 Dec;11(6):1147–1161. doi: 10.1016/0896-6273(93)90227-i. [DOI] [PubMed] [Google Scholar]
  4. Basler K., Edlund T., Jessell T. M., Yamada T. Control of cell pattern in the neural tube: regulation of cell differentiation by dorsalin-1, a novel TGF beta family member. Cell. 1993 May 21;73(4):687–702. doi: 10.1016/0092-8674(93)90249-p. [DOI] [PubMed] [Google Scholar]
  5. Blum M., Gaunt S. J., Cho K. W., Steinbeisser H., Blumberg B., Bittner D., De Robertis E. M. Gastrulation in the mouse: the role of the homeobox gene goosecoid. Cell. 1992 Jun 26;69(7):1097–1106. doi: 10.1016/0092-8674(92)90632-m. [DOI] [PubMed] [Google Scholar]
  6. Dohrmann C. E., Hemmati-Brivanlou A., Thomsen G. H., Fields A., Woolf T. M., Melton D. A. Expression of activin mRNA during early development in Xenopus laevis. Dev Biol. 1993 Jun;157(2):474–483. doi: 10.1006/dbio.1993.1150. [DOI] [PubMed] [Google Scholar]
  7. Ericson J., Thor S., Edlund T., Jessell T. M., Yamada T. Early stages of motor neuron differentiation revealed by expression of homeobox gene Islet-1. Science. 1992 Jun 12;256(5063):1555–1560. doi: 10.1126/science.1350865. [DOI] [PubMed] [Google Scholar]
  8. Goulding M. D., Chalepakis G., Deutsch U., Erselius J. R., Gruss P. Pax-3, a novel murine DNA binding protein expressed during early neurogenesis. EMBO J. 1991 May;10(5):1135–1147. doi: 10.1002/j.1460-2075.1991.tb08054.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Goulding M. D., Lumsden A., Gruss P. Signals from the notochord and floor plate regulate the region-specific expression of two Pax genes in the developing spinal cord. Development. 1993 Mar;117(3):1001–1016. doi: 10.1242/dev.117.3.1001. [DOI] [PubMed] [Google Scholar]
  10. Green J. B., New H. V., Smith J. C. Responses of embryonic Xenopus cells to activin and FGF are separated by multiple dose thresholds and correspond to distinct axes of the mesoderm. Cell. 1992 Nov 27;71(5):731–739. doi: 10.1016/0092-8674(92)90550-v. [DOI] [PubMed] [Google Scholar]
  11. Hemmati-Brivanlou A., Melton D. A. Inhibition of activin receptor signaling promotes neuralization in Xenopus. Cell. 1994 Apr 22;77(2):273–281. doi: 10.1016/0092-8674(94)90319-0. [DOI] [PubMed] [Google Scholar]
  12. Hynes M., Poulsen K., Tessier-Lavigne M., Rosenthal A. Control of neuronal diversity by the floor plate: contact-mediated induction of midbrain dopaminergic neurons. Cell. 1995 Jan 13;80(1):95–101. doi: 10.1016/0092-8674(95)90454-9. [DOI] [PubMed] [Google Scholar]
  13. Jostes B., Walther C., Gruss P. The murine paired box gene, Pax7, is expressed specifically during the development of the nervous and muscular system. Mech Dev. 1990 Dec;33(1):27–37. doi: 10.1016/0925-4773(90)90132-6. [DOI] [PubMed] [Google Scholar]
  14. Kessler D. S., Melton D. A. Vertebrate embryonic induction: mesodermal and neural patterning. Science. 1994 Oct 28;266(5185):596–604. doi: 10.1126/science.7939714. [DOI] [PubMed] [Google Scholar]
  15. Korzh V. P. Genetic control of early neuronal development in vertebrates. Curr Opin Neurobiol. 1994 Feb;4(1):21–28. doi: 10.1016/0959-4388(94)90027-2. [DOI] [PubMed] [Google Scholar]
  16. Murata M., Onomichi K., Eto Y., Shibai H., Muramatsu M. Expression of erythroid differentiation factor (EDF) in Chinese hamster ovary cells. Biochem Biophys Res Commun. 1988 Feb 29;151(1):230–235. doi: 10.1016/0006-291x(88)90583-9. [DOI] [PubMed] [Google Scholar]
  17. Ohuchi H., Noji S., Koyama E., Myokai F., Nishikawa K., Nohno T., Tashiro K., Shiokawa K., Matsuo N., Taniguchi S. Expression pattern of the activin receptor type IIA gene during differentiation of chick neural tissues, muscle and skin. FEBS Lett. 1992 Jun 1;303(2-3):185–189. doi: 10.1016/0014-5793(92)80515-i. [DOI] [PubMed] [Google Scholar]
  18. Placzek M., Jessell T. M., Dodd J. Induction of floor plate differentiation by contact-dependent, homeogenetic signals. Development. 1993 Jan;117(1):205–218. doi: 10.1242/dev.117.1.205. [DOI] [PubMed] [Google Scholar]
  19. Ruiz i Altaba A., Jessell T. M. Midline cells and the organization of the vertebrate neuraxis. Curr Opin Genet Dev. 1993 Aug;3(4):633–640. doi: 10.1016/0959-437x(93)90100-4. [DOI] [PubMed] [Google Scholar]
  20. Walther C., Gruss P. Pax-6, a murine paired box gene, is expressed in the developing CNS. Development. 1991 Dec;113(4):1435–1449. doi: 10.1242/dev.113.4.1435. [DOI] [PubMed] [Google Scholar]
  21. Wright C. V., Cho K. W., Hardwicke J., Collins R. H., De Robertis E. M. Interference with function of a homeobox gene in Xenopus embryos produces malformations of the anterior spinal cord. Cell. 1989 Oct 6;59(1):81–93. doi: 10.1016/0092-8674(89)90871-4. [DOI] [PubMed] [Google Scholar]
  22. Yamada T., Pfaff S. L., Edlund T., Jessell T. M. Control of cell pattern in the neural tube: motor neuron induction by diffusible factors from notochord and floor plate. Cell. 1993 May 21;73(4):673–686. doi: 10.1016/0092-8674(93)90248-o. [DOI] [PubMed] [Google Scholar]
  23. Yamada T., Placzek M., Tanaka H., Dodd J., Jessell T. M. Control of cell pattern in the developing nervous system: polarizing activity of the floor plate and notochord. Cell. 1991 Feb 8;64(3):635–647. doi: 10.1016/0092-8674(91)90247-v. [DOI] [PubMed] [Google Scholar]
  24. el-Deeb S., Thompson S. C., Covault J. Characterization of a cell surface adhesion molecule expressed by a subset of developing chick neurons. Dev Biol. 1992 Jan;149(1):213–227. doi: 10.1016/0012-1606(92)90278-o. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES