Protein-kinase C: Its role in activity-dependent Purkinje cell dendritic development and plasticity

Cerebellum

Volumn 2, Issue 3, 2003, Pages 206-214

  Metzger, Friedrich ^a,c   Kapfhammer, Josef P ^b  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

^b UNIVERSITY OF BASEL   (Switzerland)

^c F HOFFMANN LA ROCHE LTD   (Switzerland)

Author keywords

Cerebellar plasticity; Classical PKC; Conventional PKC; Dendrite growth; Dendritic growth; Purkinje cell dendrites

Indexed keywords

METABOTROPIC RECEPTOR; PROTEIN KINASE C; ISOENZYME;

BRAIN FUNCTION; CELL ACTIVITY; CELL DIFFERENTIATION; CELL MATURATION; CEREBELLUM; DENDRITE; ENZYME ACTIVITY; LEARNING; LONG TERM DEPRESSION; MOTOR PERFORMANCE; NERVE CELL PLASTICITY; NERVE FIBER; PRIORITY JOURNAL; PURKINJE CELL; REVIEW; SIGNAL TRANSDUCTION; SYNAPTIC POTENTIAL; ANIMAL; CEREBELLUM CORTEX; CYTOLOGY; ENZYMOLOGY; HUMAN; LONG TERM POTENTIATION; METABOLISM; PHYSIOLOGY; ULTRASTRUCTURE;

ANIMALS; CELL DIFFERENTIATION; CEREBELLAR CORTEX; DENDRITES; HUMANS; ISOENZYMES; LONG-TERM POTENTIATION; NEURONAL PLASTICITY; PROTEIN KINASE C; PURKINJE CELLS;

EID: 85047694376     PISSN: 14734222     EISSN: None     Source Type: Journal    
DOI: 10.1080/14734220310016150     Document Type: Review

References (85)

1. Kim JJ, Thompson RF. Cerebellar circuits and synaptic mechanisms involved in classical eyeblink conditioning. Trends Neurosci 1997; 20: 177-181.
2. Crépel F. Regression of functional synapses in the immature mammalian cerebellum. Trends Neurosci 1982; 5: 266-269.
3. Ito M. Cerebellar long-term depression: characterization, signal transduction, and functional roles. Physiol Rev 2001; 81: 1143-1195.
4. Sotelo C. Cerebellar synaptogenesis: what we can learn from mutant mice. J Exp Biol 1990; 153: 225-249.
5. Schmidt R. Die postnatale Genese der Kleinhirndefekte röntgen-bestrahlter Hausmäuse. J Hirnforsch 1962; 3: 163-209.
6. Hámori J. Development of synaptic organization in the partially agranular and in the transneuronally atrophied cerebellar cortex. In: Llinás R, editor. Neurobiology of Cerebellar Evolution and Development. Chicago: American Medical Association, 1969: 845-858.
7. Altman J, Anderson WJ. Experimental reorganization of the cerebellar cortex. I. Morphological effects of elimination of all microneurons with prolonged X-irradiation started at birth. J Comp Neurol 1972; 146: 355-406.
8. Rakic P, Sidman RL. Organization of cerebellar cortex secondary to deficit of granule cells in weaver mutant mice. J Comp Neurol 1973; 152: 133-161.
9. Baptista CA, Hatten ME, Blazeski R, Mason CA. Cell-cell interactions influence survival and differentiation of purified Purkinje cells in vitro. Neuron 1994; 12: 243-260.
10. Takács J, Metzger F. Morphological study of organotypic cerebellar cultures. Acta Biol Hung 2002; 53: 187-204.
11. Seil FJ, Kies MW, Bacon ML. A comparison of demyelinating and myelination-inhibiting factor induction by whole peripheral nerve tissue and P2 protein. Brain Res 1980; 210: 441-448.
12. Blank NK, Seil FJ, Herndon RM. An ultrastructural study of cortical remodeling in cytosine arabinoside induced granuloprival cerebellum in tissue culture. Neuroscience 1982; 7: 1509-1531.
13. Seil FJ. Enhanced Purkinje cell survival in granuloprival cerebellar cultures. Brain Res 1987; 432: 312-316.
14. Morrison ME, Mason CA. Granule neuron regulation of Purkinje cell development: striking a balance between neurotrophin and glutamate signaling. J Neurosci 1998; 18: 3563-3573.
15. Zuo J, De Jager PL, Takahashi KA, Jiang W, Linden DJ, Heintz N. Neurodegeneration in Lurcher mice caused by mutation in δ2 glutamate receptor gene. Nature 1997; 388: 769-773.
16. Schilling K, Dickinson MH, Connor JA, Morgan JI. Electrical activity in cerebellar cultures determines Purkinje cell dendritic growth patterns. Neuron 1991; 7: 891-902.
17. Seil FJ, Drake-Baumann R. Reduced cortical inhibitory synaptogenesis in organotypic cerebellar cultures developing in the absence of neuronal activity. J Comp Neurol 1994; 342: 366-377.
18. Metzger F, Kapfhammer JP. Protein kinase C activity modulates dendritic differentiation of rat Purkinje cells in cerebellar slice cultures. Eur J Neurosci 2000; 12: 1993-2005.
19. Vogel MW, Prittie J. Purkinje cell dendritic arbors in chick embryos following chronic treatment with an N-methyl-D-aspartate receptor antagonist. J Neurobiol 1995; 26: 537-552.
20. Hirai H, Launey T. The regulatory connection between the activity of granule cell NMDA receptors and dendritic differentiation of cerebellar Purkinje cells. J Neurosci 2000; 20: 5217-5224.
21. Schrenk K, Kapfhammer JP, Metzger F. Altered dendritic development of cerebellar Purkinje cells in slice cultures from protein kinase Cγ-deficient mice. Neuroscience 2002; 110: 675-689.
22. Huang K-P, Huang FL. How is protein kinase C activated in CNS? Neurochem Int 1993; 22: 417-433.
23. 2+-independent protein kinase Cs contain an amino-terminal domain similar to the C2 consensus sequence. Trends Biochem Sci 1993; 18: 207-208.
24. Newton AC. Protein kinase C: structure, function and regulation. J Biol Chem 1995; 270: 28495-28498.
25. Mellor H, Parker PJ. The extended protein kinase C superfamily. Biochem J 1998; 332: 281-292.
26. Mochly-Rosen D, Gordon AS. Anchoring proteins for protein kinase C: a means for isozyme selectivity. FASEB J 1998; 12: 35-42.
27. Huang FL, Yoshida Y, Nakabayashi H, Young WS, III, Huang K-P. Immunocytochemical localization of protein kinase C isozymes in rat brain. J Neurosci 1988; 8: 4734-4744.
28. Wetsel WC, Khan WA, Merchenthaler I, et al. Tissue and cellular distribution of the extended family of protein kinase C isoenzymes. J Cell Biol 1992; 117: 121-133.
29. Goto MM, Romero GG, Balaban CD. Transient changes in flocculonodular lobe protein kinase C expression during vestibular compensation. J Neurosci 1997; 17: 4367-4381.
30. Hirono M, Sugiyama T, Kishimoto Y, et al. Phospholipase Cβ4 and protein kinase Cα and/or protein kinase CβI are involved in the induction of long term depression in cerebellar Purkinje cells. J Biol Chem 2001; 276: 45236-45242.
31. Ase K, Saito N, Shearman MS, et al. Distinct cellular expression of βI- and βII subspecies of protein kinase C in rat cerebellum. J Neurosci 1988; 8: 3850-3856.
32. Barmack NH, Qian Z, Yoshimura J. Regional and cellular distribution of protein kinase C in rat cerebellar Purkinje cells. J Comp Neurol 2000; 427: 235-254.
33. Huang FL, Young WS, III, Yoshida Y, Huang K-P. Developmental expression of protein kinase C isozymes in rat cerebellum. Dev Brain Res 1990; 52: 121-130.
34. Hashimoto T, Ase K, Sawamura S, et al. Postnatal development of a brain-specific subspecies of protein kinase C in rat. J Neurosci 1988; 8: 1678-1683.
35. Kose A, Saito N, Ito H, Kikkawa U, Nishizuka Y, Tanaka C. Electron microscopic localization of type I protein kinase C in rat Purkinje cells. J Neurosci 1988; 8: 4262-4268.
36. Cardell M, Landsend AS, Eidet J, Wieloch T, Blackstad TW, Ottersen OP. High resolution immunogold analysis reveals distinct subcellular compartmentation of protein kinase Cγ and δ in rat Purkinje cells. Neuroscience 1998; 82: 709-725.
37. Chen S, Hillman DE. Compartmentation of the cerebellar cortex by protein kinase Cδ. Neuroscience 1993; 56: 177-188.
38. Chen S, Hillman DE. Immunohistochemical localization of protein kinase Cδ during postnatal development of the cerebellum. Dev Brain Res 1994; 80: 19-25.
39. Garcia MM, Cusick CG, Harlan RE. Protein kinase Cδ in rat brain: association with sensory neuronal hierarchies. J Comp Neurol 1993; 331: 375-388.
40. Merchenthaler I, Liposits Z, Reid JJ, Wetsel WC. Light and electron microscopic immunocytochemical localization of PKC immunoreactivity in the rat central nervous system. J Comp Neurol 1993; 336: 378-399.
41. Garcia MM, Harlan RE. Protein kinase C in central vestibular, cerebellar, and precerebellar pathways of the rat. J Comp Neurol 1997; 385: 26-42.
42. Balaban CD, Romero GG. A role of climbing fibers in regulation of flocculonodular lobe protein kinase C expression during vestibular compensation. Brain Res 1998; 804: 253-265.
43. Barmack NH, Qian ZY, Kim HJ, Yoshimura J. Activity-dependent distribution of protein kinase C-δ within rat cerebellar Purkinje cells following unilateral labyrinthectomy. Exp Brain Res 2001; 141: 6-20.
44. Young WS, III. Expression of three (and a putative four) protein kinase C genes in brains of rat and rabbit. J Chem Neuroanat 1988; 1: 177-194.
45. Gong J, Xu J, Bezanilla M, van Huizen R, Derin R, Li M. Differential stimulation of PKC phosphorylation of potassium channels by ZIP1 and ZIP2. Science 1999; 285: 1565-1569.
46. Naik MU, Benedikz E, Hernandez I, et al. Distribution of protein kinase Mξ and the complete protein kinase C isoform family in rat brain. J Comp Neurol 2000; 426: 243-258.
47. Moriya M, Tanaka S. Prominent expression of protein kinase Cγ mRNA in the dendrite-rich neuropil of mice cerebellum at the critical period for synaptogenesis. Neuroreport 1994; 5: 929-932.
48. Ito M. Long-term depression. Ann Rev Neurosci 1989; 12: 85-102.
49. Changeux JP, Courrege P, Danchin A. A theory of the epigenesis of neuronal networks by selective stabilization of synapses. Proc Natl Acad Sci USA 1973; 70: 2974-2978.
50. Lohof AM, Delhaye-Bouchaud N, Mariani J. Synapse elimination in the central nervous system: functional significance and cellular mechanisms. Rev Neurosci 1996; 7: 85-101.
51. Kashiwabuchi N, Ikeda K, Araki K, et al. Impairment of motor coordination, Purkinje cell synapse formation, and cerebellar long-term depression in GluRδ2 mutant mice. Cell 1995; 81: 245-252.
52. xq and phospholipase Cβ4. Prog Brain Res 2000; 124: 31-48.
53. Kurihara H, Hashimoto K, Kano M, et al. Impaired parallel fiber→Purkinje cell synapse stabilization during cerebellar development of mutant mice lacking the glutamate receptor δ2 subunit. J Neurosci 1997; 17: 9613-9623.
54. Kano M, Hashimoto K, Chen C, et al. Impaired synapse elimination during cerebellar development in PKCγ mutant mice. Cell 1995; 83: 1223-1231.
55. Kano M, Hashimoto K, Kurihara H, et al. Persistent multiple climbing fiber innervation of cerebellar Purkinje cells in mice lacking mGluR1. Neuron 1997; 18: 71-79.
56. Kano M, Hashimoto K, Watanabe M, et al. Phospholipase Cβ4 is specifically involved in climbing fiber synapse elimination in the developing cerebellum. Proc Natl Acad Sci USA 1998; 95: 15724-15729.
57. xq. Proc Natl Acad Sci USA 1997; 94: 14089-14094.
58. De Zeeuw CI, Hansel C, Bian F, et al. Expression of a protein kinase C inhibitor in Purkinje cells blocks cerebellar LTD and adaptation of the vestibulo-ocular reflex. Neuron 1998; 20: 495-508.
59. Ichise T, Kano M, Hashimoto K, et al. mGluR1 in cerebellar Purkinje cells essential for long-term depression, synapse elimination, and motor coordination. Science 2000; 288: 1832-1835.
60. Goossens J, Daniel H, Rancillac A, et al. Expression of protein kinase C inhibitor blocks cerebellar long-term depression without affecting Purkinje cell excitability in alert mice. J Neurosci 2001; 21: 5813-5823.
61. Ghoumari AM, Wehrle R, De Zeeuw CI, Sotelo C, Dusart I. Inhibition of protein kinase C prevents Purkinje cell death but does not affect axonal regeneration. J Neurosci 2002; 22: 3531-3542.
62. Ito M, Kano M. Long-lasting depression of parallel fiber Purkinje cell transmission induced by conjunctive stimulation of parallel fibers and climbing fibers in the cerebellar cortex. Neurosci Letters 1982; 33: 253-256.
63. Ito M, Sakurai M, Tongroach P. Climbing fibre induced depression of both mossy fibre responsiveness and glutamate sensitivity of cerebellar Purkinje cells. J Physiol 1982; 324: 113-134.
64. Ekerot CF, Kano M. Long-term depression of parallel fibre synapses following stimulation of climbing fibres. Brain Res 1985; 342: 357-360.
65. Linden DJ, Connor JA. Participation of postsynaptic PKC in cerebellar long-term depression in culture. Science 1991; 254: 1656-1659.
66. Linden DJ. Input-specific induction of cerebellar long-term depression does not require presynaptic alteration. Learn Mem 1994; 1: 121-128.
67. Hansel C, Linden DJ. Long-term depression of the cerebellar climbing fiber-Purkinje neuron synapse. Neuron 2000; 26: 473-482.
68. Hirai H. Modification of AMPA receptor clustering regulates cerebellar synaptic plasticity. Neurosci Res 2001; 39: 261-267.
69. Xia J, Chung HJ, Wihler C, Huganir RL, Linden DJ. Cerebellar long-term depression requires PKC-regulated interactions between GluR2/3 and PDZ domain-containing proteins. Neuron 2001; 28: 499-510.
70. Chen C, Kano M, Abeliovich A, et al. Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKCγ mutant mice. Cell 1995; 83: 1233-1242.
71. Narasimhan K, Linden DJ. Defining a minimal computational unit for cerebellar long-term depression. Neuron 1996; 17: 333-341.
72. Salin PA, Malenka RC, Nicoll RA. Cyclic AMP mediates a presynaptic form of LTP at cerebellar parallel fiber synapses. Neuron 1996; 16: 797-803.
73. Chen C, Regehr WG. The mechanism of cAMP-mediated enhancement at a cerebellar synapse. J Neurosci 1997; 17: 8687-8694.
74. Storm DR, Hansel C, Hacker B, Parent A, Linden DJ. Impaired cerebellar long-term potentiation in type I adenylyl cyclase mutant mice. Neuron 1998; 20: 1199-1210.
75. Linden DJ, Ahn S. Activation of presynaptic cAMP-dependent protein kinase is required for induction of cerebellar long-term potentiation. J Neurosci 1999; 19: 10221-10227.
76. Lev-Ram V, Wong ST, Storm DR, Tsien RY. A new form of cerebellar long-term potentiation is postsynaptic and depends on nitric oxide but not cAMP. Proc Natl Acad Sci USA 2002; 99: 8389-8393.
77. McAllister AK. Cellular and molecular mechanisms of dendrite growth. Cereb Cortex 2000; 10: 963-973.
78. Redmond L, Ghosh A. The role of notch and rho GTPase signaling in the control of dendritic development. Current Opin Neurobiol 2001; 11: 111-117.
79. Scott EK, Luo L. How do dendrites take their shape? Nature Neurosci 2001; 4: 359-365.
80. Soderling TR. CaM-kinases: modulators of synaptic plasticity. Curr Opin Neurobiol 2000; 10: 375-380.
81. Fink CC, Meyer T. Molecular mechanisms of CaMKII activation in neuronal plasticity. Curr Opin Neurobiol 2002; 12: 293-299.
82. Aakalu G, Smith WB, Nguyen N, Jiang C, Schuman EM. Dynamic visualization of local protein synthesis in hippocampal neurons. Neuron 2001; 30: 489-502.
83. Richter JD. Think globally, translate locally: what mitotic spindles and neuronal synapses have in common. Proc Natl Acad Sci USA 2001; 98: 7069-7071.
84. Wiederkehr A, Staple J, Caroni P. The motility-associated proteins GAP-43, MARCKS, and CAP-23 share unique targeting and surface activity-inducing properties. Exp Cell Res 1997; 236: 103-116.
85. Matsuoka Y, Li X, Bennett V. Adducin is an in vivo substrate for protein kinase C: phosphorylation in the MARCKS-related domain inhibits activity in promoting spectrin-actin complexes and occurs in many cells, including dendritic spines of neurons. J Cell Biol 1998; 142: 485-497.