Corrigendum to "Profiling of dynamically changed gene expression in dorsal root ganglia post peripheral nerve injury and a critical role of injury-induced glial fibrillary acidic protein in maintenance of pain behaviors" [Pain 143 (2009) 114-122] (DOI:10.1016/j.pain.2009.02.006);Profiling of dynamically changed gene expression in dorsal root ganglia post peripheral nerve injury and a critical role of injury-induced glial fibrillary acetic protein in maintenance of pain behaviors

Pain

Volumn 143, Issue 1-2, 2009, Pages 114-122

  Kim, Doo sik ^a   Figueroa, Katherine W ^a   Li, Kang Wu ^a   Boroujerdi, Amin ^a   Yolo, Tim ^a   David Luo, Z ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Dorsal root ganglia; GFAP; Injury; Neuropathic pain; Peripheral nerve; Plasticity

Indexed keywords

ANTISENSE OLIGONUCLEOTIDE; GLIAL FIBRILLARY ACIDIC PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ASTROCYTE; CELL ACTIVATION; CONTROLLED STUDY; DISEASE DURATION; GENE EXPRESSION; HYPERALGESIA; KNOCKOUT MOUSE; MALE; MICROARRAY ANALYSIS; MOUSE; NERVE CELL PLASTICITY; NERVE LIGATION; NEUROPATHIC PAIN; NONHUMAN; NUCLEOTIDE SEQUENCE; PERIPHERAL NERVE INJURY; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; SPINAL CORD; SPINAL GANGLION; UPREGULATION; WILD TYPE;

EID: 63449104335     PISSN: 03043959     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pain.2009.05.007     Document Type: Erratum

References (51)

1. Chaplan S.R., Bach F.W., Pogrel J.W., Chung J.M., and Yaksh T.L. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods 53 (1994) 55-63
2. Christopherson K.S., Ullian E.M., Stokes C.C., Mullowney C.E., Hell J.W., Agah A., Lawler J., Mosher D.F., Bornstein P., and Barres B.A. Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis. Cell 120 (2005) 421-433
3. Colburn R.W., DeLeo J.A., Rickman A.J., Yeager M.P., Kwon P., and Hickey W.F. Dissociation of microglial activation and neuropathic pain behaviors following peripheral nerve injury in the rat. J Neuroimmunol 79 (1997) 163-175
4. Costigan M., Befort K., Karchewski L., Griffin R.S., D'Urso D., Allchorne A., Sitarski J., Mannion J.W., Pratt R.E., and Woolf C.J. Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury. BMC Neurosci 3 (2002) 16
5. Crooke S.T. Progress in antisense therapeutics. Hematol Pathol 9 (1995) 59-72
6. Crooke S.T., and Bennett C.F. Progress in antisense oligonucleotide therapeutics. Annu Rev Pharmacol Toxicol 36 (1996) 107-129
7. DeArmond S.J., Lee Y.L., Kretzschmar H.A., and Eng L.F. Turnover of glial filaments in mouse spinal cord. J Neurochem 47 (1986) 1749-1753
8. Dixon W.J. Efficient analysis of experimental observations. Annu Rev Pharmacol Toxicol 20 (1980) 441-462
9. Eng L.F. Glial fibrillary acidic protein (GFAP): the major protein of glial intermediate filaments in differentiated astrocytes. J Neuroimmunol 8 (1985) 203-214
10. Eng L.F., Ghirnikar R.S., and Lee Y.L. Glial fibrillary acidic protein: GFAP-thirty-one years (1969-2000). Neurochem Res 25 (2000) 1439-1451
11. Feinstein D.L., Weinmaster G.A., and Milner R.J. Isolation of cDNA clones encoding rat glial fibrillary acidic protein: expression in astrocytes and in Schwann cells. J Neurosci Res 32 (1992) 1-14
12. Garrison C.J., Dougherty P.M., and Carlton S.M. GFAP expression in lumbar spinal cord of naive and neuropathic rats treated with MK-801. Exp Neurol 129 (1994) 237-243
13. Garrison C.J., Dougherty P.M., Kajander K.C., and Carlton S.M. Staining of glial fibrillary acidic protein (GFAP) in lumbar spinal cord increases following a sciatic nerve constriction injury. Brain Res 565 (1991) 1-7
14. Gilmore S.A., Sims T.J., and Leiting J.E. Astrocytic reactions in spinal gray matter following sciatic axotomy. Glia 3 (1990) 342-349
15. Graeber M.B., Tetzlaff W., Streit W.J., and Kreutzberg G.W. Microglial cells but not astrocytes undergo mitosis following rat facial nerve axotomy. Neurosci Lett 85 (1988) 317-321
16. Hajos F., Csillik B., and Knyihar-Csillik E. Alterations in glial fibrillary acidic protein immunoreactivity in the upper dorsal horn of the rat spinal cord in the course of transganglionic degenerative atrophy and regenerative proliferation. Neurosci Lett 117 (1990) 8-13
17. Hanani M. Satellite glial cells in sensory ganglia: from form to function. Brain Res Brain Res Rev 48 (2005) 457-476
18. Hanani M., Huang T.Y., Cherkas P.S., Ledda M., and Pannese E. Glial cell plasticity in sensory ganglia induced by nerve damage. Neuroscience 114 (2002) 279-283
19. Honore P., Rogers S.D., Schwei M.J., Salak-Johnson J.L., Luger N.M., Sabino M.C., Clohisy D.R., and Mantyh P.W. Murine models of inflammatory, neuropathic and cancer pain each generates a unique set of neurochemical changes in the spinal cord and sensory neurons. Neuroscience 98 (2000) 585-598
20. Hua X.Y., Chen P., Polgar E., Nagy I., Marsala M., Phillips E., Wollaston L., Urban L., Yaksh T.L., and Webb M. Spinal neurokinin NK1 receptor down-regulation and antinociception: effects of spinal NK1 receptor antisense oligonucleotides and NK1 receptor occupancy. J Neurochem 70 (1998) 688-698
21. Ji R.R., Zhang Q., Bedecs K., Arvidsson J., Zhang X., Xu X.J., Wiesenfeld-Hallin Z., Bartfai T., and Hökfelt T. Galanin antisense oligonucleotides reduce galanin levels in dorsal root ganglia and induce autotomy in rats after axotomy. PNAS 91 (1994) 12540-12543
22. Kim S.H., and Chung J.M. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat. Pain 50 (1992) 355-363
23. Lacroix-Fralish M.L., Tawfik V.L., Tanga F.Y., Spratt K.F., and DeLeo J.A. Differential spinal cord gene expression in rodent models of radicular and neuropathic pain. Anesthesiology 104 (2006) 1283-1292
24. Lai J., Hunter J.C., Ossipov M.H., and Porreca F. Blockade of neuropathic pain by antisense targeting of tetrodotoxin-resistant sodium channels in sensory neurons. Methods Enzymol 314 (2000) 201-213
25. Levin M.E., Jin J.G., Ji R.R., Tong J., Pomonis J.D., Lavery D.J., Miller S.W., and Chiang L.W. Complement activation in the peripheral nervous system following the spinal nerve ligation model of neuropathic pain. Pain 137 (2008) 182-201
26. Li C.Y., Song Y.H., Higuera E.S., and Luo Z.D. Spinal dorsal horn calcium channel alpha2delta-1 subunit upregulation contributes to peripheral nerve injury-induced tactile allodynia. J Neurosci 24 (2004) 8494-8499
27. Liedtke W., Edelmann W., Bieri P.L., Chiu F.C., Cowan N.J., Kucherlapati R., and Raine C.S. GFAP is necessary for the integrity of CNS white matter architecture and long-term maintenance of myelination. Neuron 17 (1996) 607-615
28. Luo Z.D., Chaplan S.R., Higuera E.S., Sorkin L.S., Stauderman K.A., Williams M.E., and Yaksh T.L. Upregulation of dorsal root ganglion (alpha)2(delta) calcium channel subunit and its correlation with allodynia in spinal nerve-injured rats. J Neurosci 21 (2001) 1868-1875
29. Luo Z.D., Chaplan S.R., Scott B.P., Cizkova D., Calcutt N.A., and Yaksh T.L. Neuronal nitric oxide synthase mRNA upregulation in rat sensory neurons after spinal nerve ligation: lack of a role in allodynia development. J Neurosci 19 (1999) 9201-9208
30. Luo Z.D., and Figueroa K.W. Multilevel genomic approach in pain research: basic science and clinical implications. Rev Analg 10 (2008) 45-58
31. Lupien C., Brenner M., Guerin S.L., and Salesse C. Expression of glial fibrillary acidic protein in primary cultures of human Muller cells. Exp Eye Res 79 (2004) 423-429
32. McCall M.A., Gregg R.G., Behringer R.R., Brenner M., Delaney C.L., Galbreath E.J., Zhang C.L., Pearce R.A., Chiu S.Y., and Messing A. Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiology. Proc Natl Acad Sci USA 93 (1996) 6361-6366
33. Murray M., Wang S.D., Goldberger M.E., and Levitt P. Modification of astrocytes in the spinal cord following dorsal root or peripheral nerve lesions. Exp Neurol 110 (1990) 248-257
34. Ohtori S., Takahashi K., Moriya H., and Myers R.R. TNF-alpha and TNF-alpha receptor type 1 upregulation in glia and neurons after peripheral nerve injury: studies in murine DRG and spinal cord. Spine 29 (2004) 1082-1088
35. Pekny M., Stanness K.A., Eliasson C., Betsholtz C., and Janigro D. Impaired induction of blood-brain barrier properties in aortic endothelial cells by astrocytes from GFAP-deficient mice. Glia 22 (1998) 390-400
36. Porreca F., Lai J., Bian D., Wegert S., Ossipov M.H., Eglen R.M., Kassotakis L., Novakovic S., Rabert D.K., Sangameswaran L., and Hunter J.C. A comparison of the potential role of the tetrodotoxin-insensitive sodium channels, PN3/SNS and NaN/SNS2, in rat models of chronic pain. PNAS 96 (1999) 7640-7644
37. Raghavendra V., Tanga F., and DeLeo J.A. Inhibition of microglial activation attenuates the development but not existing hypersensitivity in a rat model of neuropathy. J Pharmacol Exp Ther 306 (2003) 624-630 [Epub 2003 May 2006]
38. Schwei M.J., Honore P., Rogers S.D., Salak-Johnson J.L., Finke M.P., Ramnaraine M.L., Clohisy D.R., and Mantyh P.W. Neurochemical and cellular reorganization of the spinal cord in a murine model of bone cancer pain. J Neurosci 19 (1999) 10886-10897
39. Shibuki K., Gomi H., Chen L., Bao S., Kim J.J., Wakatsuki H., Fujisaki T., Fujimoto K., Katoh A., Ikeda T., Chen C., Thompson R.F., and Itohara S. Deficient cerebellar long-term depression, impaired eyeblink conditioning, and normal motor coordination in GFAP mutant mice. Neuron 16 (1996) 587-599
40. Srinivasan S.K., and Iversen P. Review of in vivo pharmacokinetics and toxicology of phosphorothioate oligonucleotides. J Clin Lab Anal 9 (1995) 129-137
41. Steward O., Torre E.R., Tomasulo R., and Lothman E. Neuronal activity up-regulates astroglial gene expression. Proc Natl Acad Sci USA 88 (1991) 6819-6823
42. Sumner B.E. The nature of the dividing cells around axotomized hypoglossal neurones. J Neuropathol Exp Neurol 33 (1974) 507-518
43. Svenningsen A.F., Colman D.R., and Pedraza L. Satellite cells of dorsal root ganglia are multipotential glial precursors. Neuron Glia Biol 1 (2004) 85-93
44. Svensson M., Eriksson P., Persson J.K., Molander C., Arvidsson J., and Aldskogius H. The response of central glia to peripheral nerve injury. Brain Res Bull 30 (1993) 499-506
45. Tanaka H., Katoh A., Oguro K., Shimazaki K., Gomi H., Itohara S., Masuzawa T., and Kawai N. Disturbance of hippocampal long-term potentiation after transient ischemia in GFAP deficient mice. J Neurosci Res 67 (2002) 11-20
46. Valder C.R., Liu J.J., Song Y.H., and Luo Z.D. Coupling gene chip analyses and rat genetic variances in identifying potential target genes that may contribute to neuropathic allodynia development. J Neurochem 87 (2003) 560-573
47. Wahlestedt C., Golanov E., Yamamoto S., Yee F., Ericson H., Yoo H., Inturrisi C.E., and Reis D.J. Antisense oligodeoxynucleotides to NMDA-R1 receptor channel protect cortical neurons from excitotoxicity and reduce focal ischaemic infarctions. Nature 363 (1993) 260-263
48. Wang H., Sun H., Della Penna K., Benz R.J., Xu J., Gerhold D.L., Holder D.J., and Koblan K.S. Chronic neuropathic pain is accompanied by global changes in gene expression and shares pathobiology with neurodegenerative diseases. Neuroscience 114 (2002) 529-546
49. Woodham P., Anderson P.N., Nadim W., and Turmaine M. Satellite cells surrounding axotomised rat dorsal root ganglion cells increase expression of a GFAP-like protein. Neurosci Lett 98 (1989) 8-12
50. Woolf C.J. The bigger the better or small but perfectly formed?. Pain 84 (2000) 445-446 [letter]
51. Xiao H.S., Huang Q.H., Zhang F.X., Bao L., Lu Y.J., Guo C., Yang L., Huang W.J., Fu G., Xu S.H., Cheng X.P., Yan Q., Zhu Z.D., Zhang X., Chen Z., and Han Z.G. Identification of gene expression profile of dorsal root ganglion in the rat peripheral axotomy model of neuropathic pain. Proc Natl Acad Sci USA 99 (2002) 8360-8365