Olig2/Plp-positive progenitor cells give rise to bergmann glia in the cerebellum

Cell Death and Disease

Volumn 4, Issue 3, 2013, Pages

  Chung, S H ^a   Guo, F ^a   Jiang, P ^a   Pleasure, D E ^a,b   Deng, W ^a,b,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b SHRINERS HOSPITALS FOR CHILDREN NORTHERN CALIFORNIA   (United States)

^c HUBEI UNIVERSITY OF ARTS AND SCIENCE   (China)

Author keywords

Bergmann glia; Cerebellum; Olig2 progenitor cell

Indexed keywords

OLIGODENDROCYTE TRANSCRIPTION FACTOR 2; TAMOXIFEN; ANTIGEN; BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; CHONDROITIN SULFATE PROTEOGLYCAN 4; CRE RECOMBINASE; GLUTAMIC ACID; INTEGRASE; NERVE PROTEIN; OLIG2 PROTEIN, MOUSE; PLP1 PROTEIN, MOUSE; PROTEOGLYCAN; PROTEOLIPID PROTEIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; ASTROCYTE; CELL FATE; CEREBELLUM; CLINICAL ASSESSMENT; CONTROLLED STUDY; FEMALE; GENE MAPPING; IN VIVO STUDY; MALE; MOUSE; NEURAL STEM CELL; NONHUMAN; OLIGODENDROGLIA; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PROGENY; ANIMAL; CELL DIFFERENTIATION; CELL LINE; CELL LINEAGE; CYTOLOGY; GENE EXPRESSION REGULATION; GENETICS; HYPOXIC ISCHEMIC ENCEPHALOPATHY; METABOLISM; NERVOUS SYSTEM DEVELOPMENT; NEWBORN; PATHOLOGY; SIGNAL TRANSDUCTION; TRANSGENIC MOUSE;

MUS MUSCULUS;

ANIMALS; ANIMALS, NEWBORN; ANTIGENS; ASTROCYTES; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CELL DIFFERENTIATION; CELL LINE; CELL LINEAGE; CEREBELLUM; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GLUTAMIC ACID; HYPOXIA-ISCHEMIA, BRAIN; INTEGRASES; MICE; MICE, TRANSGENIC; MYELIN PROTEOLIPID PROTEIN; NERVE TISSUE PROTEINS; NEURAL STEM CELLS; NEUROGENESIS; OLIGODENDROGLIA; PROTEOGLYCANS; SIGNAL TRANSDUCTION;

EID: 84875881006     PISSN: None     EISSN: 20414889     Source Type: Journal    
DOI: 10.1038/cddis.2013.74     Document Type: Article

References (50)

1. Levine JM, Reynolds R, Fawcett JW. The oligodendrocyte precursor cell in health and disease. Trends Neurosci 2001; 24: 39-47.
2. Stallcup WB. The NG2 proteoglycan: past insights and future prospects. J Neurocytol 2002; 31: 423-435.
3. Raff MC, Miller RH, Noble M. A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium. Nature 1983; 303: 390-396.
4. Kondo T, Raff M. Oligodendrocyte precursor cells reprogrammed to become multipotential CNS stem cells. Science 2000; 289: 1754-1757.
5. Belachew S, Chittajallu R, Aguirre AA, Yuan X, Kirby M, Anderson S et al. Postnatal NG2 proteoglycan-expressing progenitor cells are intrinsically multipotent and generate functional neurons. J Cell Biol 2003; 161: 169-186.
6. Aguirre A, Gallo V. Postnatal neurogenesis and gliogenesis in the olfactory bulb from NG2-expressing progenitors of the subventricular zone. J Neurosci 2004; 24: 10530-10541.
7. Aguirre AA, Chittajallu R, Belachew S, Gallo V. NG2-expressing cells in the subventricular zone are type C-like cells and contribute to interneuron generation in the postnatal hippocampus. J Cell Biol 2004; 165: 575-589.
8. Rivers LE, Young KM, Rizzi M, Jamen F, Psachoulia K, Wade A et al. PDGFRA/NG2 glia generate myelinating oligodendrocytes and piriform projection neurons in adult mice. Nat Neurosci 2008; 11: 1392-1401.
9. Guo F,Maeda Y, Ma J, Xu J, Horiuchi M, Miers L et al. Pyramidal neurons are generated from oligodendroglial progenitor cells in adult piriform cortex. J Neurosci 2010; 30: 12036-12049.
10. Michalski JP, Anderson C, Beauvais A, De Repentigny Y, Kothary R. The proteolipid protein promoter drives expression outside of the oligodendrocyte lineage during embryonic and early postnatal development. PLoS One 2011; 6: e19772.
11. Zhu X, Bergles DE, Nishiyama A. NG2 cells generate both oligodendrocytes and gray matter astrocytes. Development 2008a; 135: 145-157.
12. Zhu X, Hill RA, Nishiyama A. NG2 cells generate oligodendrocytes and gray matter astrocytes in the spinal cord. Neuron Glia Biol 2008b; 4: 19-26.
13. Guo F, Ma J, McCauley E, Bannerman P, Pleasure D. Early postnatal proteolipid promoterexpressing progenitors produce multilineage cells in vivo. J Neurosci 2009; 29: 7256-7270.
14. Kang SH, Fukaya M, Yang JK, Rothstein JD, Bergles DE. NG2CNS glial progenitors remain committed to the oligodendrocyte lineage in postnatal life and following neurodegeneration. Neuron 2010; 68: 668-681.
15. Doerflinger NH, Macklin WB, Popko B. Inducible site-specific recombination in myelinating cells. Genesis 2003; 35: 63-72.
16. Lu QR, Yuk D, Alberta JA, Zhu Z, Pawlitzky I, Chan J et al. Sonic hedgehog-regulated oligodendrocyte lineage genes encoding bHLH proteins in the mammalian central nervous system. Neuron 2000; 25: 317-329.
17. Zhou Q, Wang S, Anderson DJ. Identification of a novel family of oligodendrocyte lineagespecific basic helix-loop-helix transcription factors. Neuron 2000; 25: 331-343.
18. Takebayashi H, Nabeshima Y, Yoshida S, Chisaka O, Ikenaka K, Nabeshima Y. The basic helix-loop-helix factor olig2 is essential for the development of motoneuron and oligodendrocyte lineages. Curr Biol 2002; 12: 1157-1163.
19. Liu W, Shen Y, Plane JM, Pleasure DE, Deng W. Neuroprotective potential of erythropoietin and its derivative carbamylated erythropoietin in periventricular leukomalacia. Exp Neurol 2011; 30: 227-239.
20. Shen Y, Liu XB, Pleasure DE, Deng W. Axon-glia synapses are highly vulnerable to white matter injury in the developing brain. J Neurosci Res 2012; 90: 105-121.
21. Mallon BS, Shick HE, Kidd GJ, Macklin WB. Proteolipid promoter activity distinguishes two populations of NG2-positive cells throughout neonatal cortical development. J Neurosci 2002; 22: 876-885.
22. Hirrlinger PG, Scheller A, Braun C, Quintela-Schneider M, Fuss B, Hirrlinger J et al. Expression of reef coral fluorescent proteins in the central nervous system of transgenic mice. Mol Cell Neurosci 2005; 30: 291-303.
23. Le Bras B, Chatzopoulou E, Heydon K, Martínez S, Ikenaka K, Prestoz L et al. Oligodendrocyte development in the embryonic brain: the contribution of the plp lineage. Int J Dev Biol 2005; 49: 209-220.
24. Baracskay KL, Kidd GJ, Miller RH, Trapp BD. NG2-positive cells generate A2B5-positive oligodendrocyte precursor cells. Glia 2007; 55: 1001-1010.
25. Yamada K, Watanabe M. Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells. Anat Sci Int 2002; 77: 94-108.
26. Ozol K, Hayden JM, Oberdick J, Hawkes R. Transverse zones in the vermis of the mouse cerebellum. J Comp Neurol 1999; 412: 95-111.
27. Chung SH, Marzban H, Croci L, Consalez GG, Hawkes R. Purkinje cell subtype specification in the cerebellar cortex: Ebf2 acts to repress the zebrin II-positive Purkinje cell phenotype. Neuroscience 2008; 153: 721-732.
28. Chung SH, Calafiore M, Plane JM, Pleasure DE, Deng W. Apoptosis inducing factor deficiency causes reduced Mitofusion 1 expression and patterned Purkinje cell degeneration. Neurobiol Dis 2011; 41: 445-457.
29. Muller T, Moller T, Berger T, Schnitzer J, Kettenmann H. Calcium entry through kainate receptors and resulting potassium channel blockade in Bergmann glial cells. Science 1992; 256: 1563-1566.
30. Rothstein JD, Martin L, Levey AI, Dykes-Hoberg M, Jin L, Wu D et al. Localization of neuronal and glial glutamate transporters. Neuron 1994; 13: 713-725.
31. Magnus T, Carmen J, Deleon J, Xue H, Pardo AC, Lepore AC et al. Adult glial precursor proliferation in mutant SOD1G93A mice. Glia 2008; 56: 200-208.
32. Sellers DL, Maris DO, Horner PJ. Postinjury niches induce temporal shifts in progenitor fates to direct lesion repair after spinal cord injury. J Neurosci 2009; 29: 6722-6733.
33. Zawadzka M, Rivers LE, Fancy SP, Zhao C, Tripathi R, Jamen F et al. CNS-resident glial progenitor/stem cells produce Schwann cells as well as oligodendrocytes during repair of CNS demyelination. Cell Stem Cell 2010; 6: 578-590.
34. Deng W, Pleasure J, Pleasure D. Progress in periventricular leukomalacia. Arch Neurol 2008; 65: 1291-1295.
35. Deng W. Neurobiology of injury to the developing brain. Nat Rev Neurol 2010; 6: 328-336.
36. Volpe JJ. Brain injury in premature infants: a complex amalgam of destructive and developmental disturbances. Lancet Neurol 2009; 8: 110-124.
37. Rivest S. Molecular insights on the cerebral innate immune system. Brain Behav Immun 2003; 17, pp 13-19.
38. Billiards SS, Haynes RL, Folkerth RD, Trachtenberg FL, Liu LG, Volpe JJ. Development of microglia in the cerebral white matter of the human fetus and infant. J Comp Neurol 2006; 497: 199-208.
39. Richardson WD, Young KM, Tripathi RB, McKenzie I. NG2-glia as multipotent neural stem cells: fact or fantasyNeuron 2011; 70: 661-673.
40. Tamura Y, Kataoka Y, Cui Y, Takamori Y, Watanabe Y, Yamada H. Multi-directional differentiation of doublecortin- and NG2-immunopositive progenitor cells in the adult rat neocortex in vivo. Eur J Neurosci 2007; 25: 3489-3498.
41. Komitova M, Zhu X, Serwanski DR, Nishiyama A. NG2 cells are distinct from neurogenic cells in the postnatal mouse subventricular zone. J Comp Neurol 2009; 512: 702-716.
42. Dimou L, Simon C, Kirchhoff F, Takebayashi H, Gotz M. Progeny of Olig2-expressing progenitors in the gray and white matter of the adult mouse cerebral cortex. J Neurosci 2008; 28: 10434-10442.
43. Yuasa S, Kawamura K, Kuwano R, Ono K. Neuron-glia interrelations during migration of Purkinje cells in the mouse embryonic cerebellum. Int J Dev Neurosci 1996; 14: 429-438.
44. Altman J, Bayer SA. Development of the Cerebellar System. Relation to Its Evolution, Structure, and Functions. CRC Press: Boca Raton, 1997 pp121-150.
45. Yamada K, Fukaya M, Shibata T. Dynamic transformation of Bergmann glial fibers proceeds in correlation with dendritic outgrowth and synapse formation of cerebellar Purkinje cells. J Comp Neurol 2000; 418: 106-120.
46. Karadottir R, Cavelier P, Bergersen LH, Attwell D. NMDA receptors are expressed in oligodendrocytes and activated in ischaemia. Nature 2005; 438: 1162-1166.
47. De Biase LM, Kang SH, Baxi EG, Fukaya M, Pucak ML, Mishina M et al. NMDA receptor signaling in oligodendrocyte progenitors is not required for oligodendrogenesis and myelination. J Neurosci 2011; 31: 12650-12662.
48. Guo F, Maeda Y, Ko EM, Delgado M, Horiuchi M, Soulika A. Disruption of NMDA receptors in oligodendroglial lineage cells does not alter their susceptibility to experimental autoimmune encephalomyelitis or their normal development. J Neurosci 2012; 32: 639-645.
49. Srinivas S, Watanabe T, Lin CS, William CM, Tanabe Y, Jessell TM et al. Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus. BMC Dev Biol 2001; 1: 4.
50. Sillitoe RV, Benson MA, Blake DJ, Hawkes R. Abnormal dysbindin expression in cerebellar mossy fiber synapses in the mdx mouse model of Duchenne muscular dystrophy. J Neurosci 2003; 23: 6576-6585.