Origins and control of the differentiation of inhibitory interneurons and glia in the cerebellum

Developmental Biology

Volumn 328, Issue 2, 2009, Pages 422-433

  Grimaldi, Piercesare ^a,b   Parras, Carlos ^c   Guillemot, François ^d   Rossi, Ferdinando ^b   Wassef, Marion ^a  

^a ECOLE NORMALE SUPÉRIEURE   (France)

^b UNIVERSITY OF TURIN   (Italy)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^d NATIONAL INSTITUTE FOR MEDICAL RESEARCH   (United Kingdom)

Author keywords

Ascl1; Astrocyte; Cerebellum development; Differentiation; GABAergic interneuron; Oligodendrocyte; Specification

Indexed keywords

4 AMINOBUTYRIC ACID RECEPTOR; TRANSCRIPTION FACTOR MASH1;

ANIMAL TISSUE; ARTICLE; ASTROCYTE; CELL DIFFERENTIATION; CELL FATE; CELL LINEAGE; CELL TYPE; CELLULAR DISTRIBUTION; CEREBELLUM; CONTROLLED STUDY; ELECTROPORATION; EMBRYO; EXPRESSION VECTOR; FEMALE; GENE EXPRESSION; GENE FUNCTION; GLIA; INTERNEURON; MALE; MOUSE; NEUROEPITHELIUM; NONHUMAN; OLIGODENDROGLIA; PRIORITY JOURNAL;

EPICOCCUM;

EID: 63549107794     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2009.02.008     Document Type: Article

References (51)

1. Alexandre P., Bachy I., Marcou M., and Wassef M. Positive and negative regulations by FGF8 contribute to midbrain roof plate developmental plasticity. Development 133 (2006) 2905-2913
2. Basson M.A., Echevarria D., Ahn C., Sudarov A., Joyner A.L., Mason I.J., Martinez S., and Martin G.R. Specific regions within the embryonic midbrain and cerebellum require different levels of FGF signaling during development. Development 135 (2008) 889-898
3. Battiste J., Helms A.W., Kim E.J., Savage T.K., Lagace D.C., Mandyam C.D., Eisch A.J., Miyoshi G., and Johnson J.E. Ascl1 defines sequentially generated lineage-restricted neuronal and oligodendrocyte precursor cells in the spinal cord. Development 134 (2007) 285-293
4. Carletti B., Grimaldi P., Magrassi L., and Rossi F. Specification of cerebellar progenitors after heterotopic-heterochronic transplantation to the embryonic cns in vivo and in vitro. J. Neurosci. 22 (2002) 7132-7146
5. Carletti B., Williams I.M., Leto K., Nakajima K., Magrassi L., and Rossi F. Time constraints and positional cues in the developing cerebellum regulate Purkinje cell placement in the cortical architecture. Dev. Biol. 317 (2008) 147-160
6. Casarosa S., Fode C., and Guillemot F. Mash1 regulates neurogenesis in the ventral telencephalon. Development 126 (1999) 525-534
7. Castro D.S., Skowronska-Krawczyk D., Armant O., Donaldson I.J., Parras C., Hunt C., Critchley J.A., Nguyen L., Gossler A., Göttgens B., Matter J.M., and Guillemot F. Proneural bHLH and Brn proteins coregulate a neurogenic program through cooperative binding to a conserved DNA motif. Dev. Cell. 11 (2006) 831-844
8. Cheung M., and Briscoe J. Neural crest development is regulated by the transcription factor Sox9. Development 130 (2003) 5681-5693
9. Celio M.R. Calbindin D-28k and Parvalbumin in the rat nervous system. Neuroscience 35 (1990) 345-375
10. Cohen-Tannoudji M., Babinet C., and Wassef M. Early determination of a mouse somatosensory cortex marker. Nature 368 (1994) 460-463
11. Fode C., Ma Q., Casarosa S., Ang S.-L., Anderson D.J., and Guillemot F. A role for neural determination genes in specifying the dorsoventral identity of telencephalic neurons. Genes Dev. 14 (2000) 67-80
12. Gong S., Zheng C., Doughty M.L., Losos K., Didkovsky N., Schambra U.B., Nowak N.J., Joyner A., Leblanc G., Hatten M.E., and Heintz N. A gene expression atlas of the central nervous system based on bacterial artificial chromosomes. Nature 30 (2003) 917-925
13. Hadjantonakis A.K., Gertenstein M., Ikawa M., Okabe M., and Nagy A. Generating green fluorescent mice by germline transmission of green fluorescent ES cells. Mech. Dev. 76 (1998) 79-90
14. Hashimoto M., and Mikoshiba K. Neuronal birthdate-specific gene transfer with adenoviral vectors. J. Neurosci. 24 (2004) 286-296
15. Hoshino M., Nakamura S., Mori K., Kawauchi T., Terao M., Nishimura Y.V., Fukuda A., Fuse T., Matsuo N., Sone M., Watanabe M., Bito H., Terashima T., Wright C.V.E., Kawaguchi Y., Nakao K., and Nabeshima Y. Ptf1a, a bHLH transcriptional gene, defines gabaergic neuronal fates in cerebellum. Neuron 47 (2005) 201-213
16. Jankovski A., Rossi F., and Sotelo C. Neuronal precursors in the postnatal mouse cerebellum are fully committed cells: evidence from heterochronic transplantations. Eur. J. Neurosci. 8 (1996) 2308-2319
17. Jessberger S., Toni N., Clemenson Jr. G.D., Ray J., and Gage F.H. Directed differentiation of hippocampal stem/progenitor cells in the adult brain. Nat. Neurosci. 11 (2008) 888-893
18. Kim E.J., Battiste J., Nakagawa Y., and Johnson J.E. Ascl1 (Mash1) lineage cells contribute to discrete cell populations in CNS architecture. Mol. Cell. Neurosci. 38 (2008) 595-606
19. Lee A., Kessler J.D., Read T.-A., Kaiser C., Corbeil D., Huttner W.B., Johnson J.E., and Wechsler-Reya R.J. Isolation of neural stem cells from the postnatal cerebellum. Nat. Neurosci. 8 (2005) 723-729
20. Leto K., Carletti B., Williams I.M., Magrassi L., and Rossi F. Different types of cerebellar GABAergic interneurons originate from a common pool of multipotent progenitor cells. J. Neurosci. 26 (2006) 11682-11694
21. Lo L., Dormand E., Greenwood A., and Anderson D.J. Comparison of the generic neuronal differentiation and neuron subtype specification functions of mammalian achaete-scute and atonal homologs in cultured neural progenitor cells. Development 129 (2002) 1553-1567
22. Lo L., Sommer L., and Anderson D.J. MASH1 maintains competence for BMP2-induced neuronal differentiation in post-migratory neural crest cells. Curr. Biol. 7 (1997) 440-450
23. Louvi A., Alexandre P., Metin C., Wurst W., and Wassef M. The isthmic neuroepithelium is essential for cerebellar midline fusion. Development 130 (2003) 5319-5330
24. Maricich S.M., and Herrup K. Pax-2 expression defines a subset of GABAergic interneurons and their precursors in the developing murine cerebellum. J. Neurobiol. 41 (1999) 281-294
25. Milosevic A., and Goldman E.G. Progenitors in the postnatal cerebellar white matter are antigenically heterogeneous. J. Comp. Neurol. 452 (2002) 192-203
26. Milosevic A., and Goldman J.E. Potential of progenitors from postnatal cerebellar neuroepithelium and white matter: lineage specified vs. multipotent fate. Mol. Cell. Neurosci. 26 (2004) 342-353
27. Miyoshi G., Bessho Y., Yamada S., and Kageyama R. Identification of a novel basic helix-loop-helix gene, heslike, and its role in GABAergic neurogenesis. J. Neurosci. 24 (2004) 3672-3682
28. Mizuguchi R., Kriks S., Cordes R., Gossler A., Ma Q., and Goulding M. Ascl1 and Gsh1/2 control inhibitory and excitatory cell fate in spinal sensory interneurons. Nat. Neurosci. 9 (2006) 770-778
29. Nieto S.B., and Guillemot. Neural bHLH genes control the neuronal versus glial fate decision in cortical progenitors. Neuron 29 (2001) 401-413
30. Parras C.M., Hunt C., Sugimori M., Nakafuku M., Rowitch D., and Guillemot F. The proneural gene mash1 specifies an early population of telencephalic oligodendrocytes. J. Neursci. 27 (2007) 4233-4242
31. Parras, C.M., Schuurmans, C., Scardigli, R., Kim, J., Anderson, D.J., Guillemot, F., 2002. Divergent functions of the proneural genes Mash1 and Ngn2 in the specification of neuronal subtype identity. 16, 324-338.
32. Parras G., Britz, Soares, Galichet, Battiste, Johnson, Nakafuku, Bescovi, and Guillemot. Mash1 specifies neurons and oligodendrocytes in the postnatal brain. EMBO J. 23 (2004) 4495-4505
33. Petryniak M.A., Potter G.B., Rowitch D.H., and Rubenstein J.L.R. Dlx1 and Dlx2 Control Neuronal versus oligodendroglial cell fate acquisition in the developing forebrain. Neuron 55 (2007) 417-433
34. Pfeffer P.L., Payer B., Reim G., di Magliano M.P., and Busslinger M. The activation and maintenance of Pax2 expression at the mid-hindbrain boundary is controlled by separate enhancers. Development 129 (2002) 307-318
35. Reynolds W., and Wilkin G.P. Development of macroglial cells in rat cerebellum II. An in situ immunohisotchemical study of oligodendroglial lineage from precursor to mature myelinating cell. Development 102 (1988) 409-425
36. Solbach S., and Celio M.R. Ontogeny of the calcium binding protein parvalbumin in the rat nervous system. Anat. Embryol. 184 (1991) 103-124
37. Spokony R.F., Aoki Y., Saint-Germain N., Magner-Fink E., and Saint-Jeannet J.P. The transcription factor Sox9 is required for cranial neural crest development in Xenopus. Development 129 (2002) 421-432
38. Stolt C.C., Lommes P., Sock E., Chaboissier M.C., Schedl A., and Wegner M. The Sox9 transcription factor determines glial fate choice in the developing spinal cord. Genes Dev. 17 (2003) 1677-1689
39. +-dependent glutamate/aspartate transporter from rat brain. Proc. Natl. Acad. Sci. 89 (1992) 10955-10959
40. Sugimori M., Nagao M., Bertrand N., Parras C.M., Guillemot F., and Nakafuku M. Combinatorial actions of patterning and HLH transcription factors in the spatiotemporal control of neurogenesis and gliogenesis in the developing spinal cord. Development 134 (2007) 1617-1629
41. Sugimori M., Nagao M., Parras C.M., Nakatani H., Lebel M., Guillemot F., and Nakafuku M. Ascl1 is required for oligodendrocyte development in the spinal cord. Development 135 (2008) 1271-1281
42. Vallstedt A., Klos J.M., and Ericson J. Multiple dorsoventral origins of oligodendrocyte generation in the spinal cord and hindbrain. Neuron 45 (2005) 55-67
43. van Heyningen P., Calver A.R., and Richardson W.D. Control of progenitor cell number by mitogen supply and demand. Curr. Biol. 11 (2001) 232-241
44. Wassef M., Zanetta J.P., Brehier A., and Sotelo C. Transient biochemical compartmentalization of Purkinje cells during early cerebellar development. Dev. Biol. 111 (1985) 129-137
45. Wilkinson D.G. In Situ Hybridization: a Practical Approach (1992), Oxford University Press, New York
46. Weisheit G., Gliem M., Endl E., Pfeffer P.L., Busslinger M., and Schilling K. Postnatal development of the murine cerebellar cortex: formation and early dispersal of basket, stellate and Golgi neurons. Eur. J. Neurosci. 24 (2006) 466-478
47. Wildner H., Muller T., Cho S.-H., Brohl D., Cepko C.L., Guillemot F., and Birchmeier C. dILA neurons in the dorsal spinal cord are the product of terminal and non-terminal asymmetric progenitor cell divisions, and require Mash1 for their development. Development 133 (2006) 2105-2113
48. Zhang L.G., and Goldman J.E. Generation of cerebellar interneurons from dividing progenitors in white matter. Neuron 16 (1996) 47-54
49. Zhang L.G., and Goldman J.E. Developmental fates and migratory pathways of dividing progenitors in the postnatal rat cerebellum. J. Comp. Neurol. 370 (1996) 536-550
50. Zhou Q., and Anderson D.J. The bHLH transcription factors OLIG2 and OLIG1 couple neuronal and glial subtype specification. Cell 109 (2002) 61-73
51. Zordan C., Hawkes, and Consalez. Comparative analysis of proneural gene expression in the embryonic cerebellum. Dev. Dyn. 237 (2008) 1726-1735