Activating transcription factor 3 (ATF3) induction by axotomy in sensory and motoneurons: A novel neuronal marker of nerve injury

Molecular and Cellular Neurosciences

Volumn 15, Issue 2, 2000, Pages 170-182

  Tsujino, Hiroaki ^a,b   Kondo, Eiji ^a   Fukuoka, Tetsuo ^a   Dai, Yi ^a   Tokunaga, Atsushi ^a   Miki, Kenji ^a   Yonenobu, Kazuo ^b   Ochi, Takahiro ^b   Noguchi, Koichi ^a  

^a HYOGO COLLEGE OF MEDICINE   (Japan)

^b OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMICAL MARKER; CYCLIC AMP RESPONSIVE ELEMENT BINDING PROTEIN; TRANSCRIPTION FACTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; DIAGNOSTIC VALUE; DISEASE ACTIVITY; DISEASE MARKER; NERVE FIBER TRANSECTION; NERVE INJURY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT;

ANIMALIA; STAPHYLOCOCCUS PHAGE 3A;

EID: 0033956898     PISSN: 10447431     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcne.1999.0814     Document Type: Article

References (37)

1. Brindle P. K., Montminy M. R. The CREB family of transcription activators. Curr. Opin. Genet. Dev. 2:1992;199-204.
2. Chen B. P., Liang G., Whelan J., Hai T. ATF3 and ATF3 delta Zip. Transcriptional repression versus activation by alternatively spliced isoforms. J. Biol. Chem. 269:1994;15819-15826.
3. Chen B. P., Wolfgang C. D., Hai T. Analysis of ATF3, a transcription factor induced by physiological stresses and modulated by gadd153/Chop10. Mol. Cell. Biol. 16:1996;1157-1168.
4. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:1987;156-159.
5. Chu H. M., Tan Y., Kobierski L. A., Balsam L. B., Comb M. J. Activating transcription factor-3 stimulates 3′,5′-cyclic adenosine monophosphate-dependent gene expression. Mol. Endocrinol. 8:1994;59-68.
6. Coni P., Simbula G., de Prati A. C., Menegazzi M., Suzuki H., Sarma D. S., Ledda C. G., Columbano A. Differences in the steady-state levels of c-fos, c-jun and c-myc messenger RNA during mitogen-induced liver growth and compensatory regeneration. Hepatology. 17:1993;1109-1116.
7. Das D. K., Maulik N., Moraru I. I. Gene expression in acute myocardial stress. Induction by hypoxia, ischemia, reperfusion, hyperthermia and oxidative stress. J. Mol. Cell. Cardiol. 27:1995;181-193.
8. De Leon M., Nahin R. L., Molina C. A., De Leon D., Ruda M. A. Comparison of c-jun, junB, and junD mRNA expression and protein in the rat dorsal root ganglia following sciatic nerve transection. J. Neurosci. Res. 42:1995;391-401.
9. Dragunow M., Beilharz E., Sirimanne E., Lawlor P., Williams C., Bravo R., Gluckman P. Immediate-early gene protein expression in neurons undergoing delayed death, but not necrosis, following hypoxic-ischaemic injury to the young rat brain. Mol. Brain Res. 25:1994;19-33.
10. Drysdale B. E., Howard D. L., Johnson R. J. Identification of a lipopolysaccharide inducible transcription factor in murine macrophages. Mol. Immunol. 33:1996;989-998.
11. Fornace A. J., Alamo I. J., Hollander M. C. DNA damage-inducible transcripts in mammalian cells. Proc. Natl. Acad. Sci. USA. 85:1988;8800-8804.
12. Fornace A. J., Nebert D. W., Hollander M. C., Luethy J. D., Papathanasiou M., Fargnoli J., Holbrook N. J. Mammalian genes coordinately regulated by growth arrest signals and DNA-damaging agents. Mol. Cell. Biol. 9:1989;4196-4203.
13. Hai T. W., Liu F., Coukos W. J., Green M. R. Transcription factor ATF cDNA clones: An extensive family of leucine zipper proteins able to selectively form DNA-binding heterodimers. Genes Dev. 3:1989;2083-2090.
14. Hai T., Curran T. Cross-family dimerization of transcription factors Fos/Jun and ATF/CREB alters DNA binding specificity. Proc. Natl. Acad. Sci. USA. 88:1991;3720-3724.
15. Herdegen T., Kovary K., Leah J., Bravo R. Specific temporal and spatial distribution of JUN, FOS, and KROX-24 proteins in spinal neurons following noxious transsynaptic stimulation. J. Comp. Neurol. 313:1991;178-191.
16. Herdegen T., Fiallos E. C., Schmid W., Bravo R., Zimmermann M. The transcription factors c-JUN, JUN D and CREB, but not FOS and KROX-24, are differentially regulated in axotomized neurons following transection of rat sciatic nerve. Mol. Brain Res. 14:1992;155-165.
17. Herdegen T., Fiallos E. C., Bravo R., Zimmermann M. Colocalisation and covariation of c-JUN transcription factor with galanin in primary afferent neurons and with CGRP in spinal motoneurons following transection of rat sciatic nerve. Mol. Brain Res. 17:1993;147-154.
18. Herdegen T., Zimmermann M. Expression of c-Jun and JunD transcription factors represent specific changes in neuronal gene expression following axotomy. Prog. Brain Res. 103:1994;153-171.
19. Herdegen T., Leah J. D. Inducible and constitutive transcription factors in the mammalian nervous system: Control of gene expression by Jun, Fos and Krox, and CREB/ATF proteins. Brain Res. Rev. 28:1998;370-490.
20. Himes B. T., Tessler A. Death of some dorsal root ganglion neurons and plasticity of others following sciatic nerve section in adult and neonatal rats. J. Comp. Neurol. 284:1989;215-230.
21. Hokfelt T., Zhang X., Wiesenfeld H. Z. Messenger plasticity in primary sensory neurons following axotomy and its functional implications. Trends Neurosci. 17:1994;22-30.
22. Hsu J. C., Laz T., Mohn K. L., Taub R. Identification of LRF-1, a leucine-zipper protein that is rapidly and highly induced in regenerating liver. Proc. Natl. Acad. Sci. USA. 88:1991;3511-3515.
23. Janig W., McLachlan E. On the fate of sympathetic and sensory neurons projecting into a neuroma of the superficial peroneal nerve in the cat. J. Comp. Neurol. 225:1984;302-311.
24. Jenkins R., Hunt S. P. Long-term increase in the levels of c-jun mRNA and jun protein-like immunoreactivity in motor and sensory neurons following axon damage. Neurosci. Lett. 129:1991;107-110.
25. Kenney A. M., Kocsis J. D. Timing of c-jun protein induction in lumbar dorsal root ganglia after sciatic nerve transection varies with lesion distance. Brain Res. 751:1997;90-95.
26. Kreutzberg G. W. Reaction of the neuronal cell body to axonal damage. Waxman S. G. The Axon, Structure, Function and Pathophysiology. 1995;355-374 Oxford Univ. Press, New York.
27. Leah J. D., Herdegen T., Bravo R. Selective expression of Jun proteins following axotomy and axonal transport block in peripheral nerves in the rat: evidence for a role in the regeneration process. Brain Res. 566:1991;198-207.
28. Liang G., Wolfgang C. D., Chen B. P., Chen T. H., Hai T. ATF3 gene. Genomic organization, promoter, and regulation. J. Biol. Chem. 271:1996;1695-1701.
29. Lieberman A. R. The axon reaction: A review of the principal features of perikaryal responses to axon injury. Int. Rev. Neurobiol. 14:1971;49-124.
30. Lowrie M. B., Vrbova G. Dependence of postnatal motoneurones on their targets: Review and hypothesis. Trends. Neurosci. 15:1992;80-84.
31. Ron D., Habener J. F. CHOP, a novel developmentally regulated nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative inhibitor of gene transcription. Genes Dev. 6:1992;439-453.
32. Sheng M., Greenberg M. E. The regulation and function of c-fos and other immediate early genes in the nervous system. Neuron. 4:1990;477-485.
33. Snider W. D., Elliott J. L., Yan Q. Axotomy-induced neuronal death during development. J. Neurobiol. 23:1992;1231-1246.
34. Wolfgang C. D., Chen B. P., Martindale J. L., Holbrook N. J., Hai T. gadd153/Chop10, a potential target gene of the transcriptional repressor ATF3. Mol. Cell. Biol. 17:1997;6700-6707.
35. Wu W., Mathew T. C., Miller F. D. Evidence that the loss of homeostatic signals induces regeneration-associated alterations in neuronal gene expression. Dev. Biol. 158:1993;456-466.
36. Yin T., Sandhu G., Wolfgang C. D., Burrier A., Webb R. L., Rigel D. F., Hai T., Whelan J. Tissue-specific pattern of stress kinase activation in ischemic/reperfused heart and kidney. J. Biol. Chem. 272:1997;19943-19950.
37. Ziff E. B. Transcription factors: A new family gathers at the cAMP response site. Trends Genet. 6:1990;69-72.