Neuronal diseases: Small heat shock proteins calm your nerves

Current Biology

Volumn 14, Issue 15, 2004, Pages

  Der Perng, Ming ^a   Quinlan, Roy A ^a  

^a DURHAM UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 4143087186     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cub.2004.07.047     Document Type: Review

References (20)

1. Kappe G., Franck E., Verschuure P., Boelens W.C., Leunissen J.A., de Jong W.W. The human genome encodes 10 alpha-crystallin-related small heat shock proteins: HspB1-10. Cell Stress Chaperones. 8:2003;53-61
2. Benn S.C., Perrelet D., Kato A.C., Scholz J., Decosterd I., Bakowska J.C., Woolf C. HSP27 upregulation and phosphorylation is required for injured sensory and motor neuron survival. Neuron. 36:2002;45-56
3. Wyttenbach A., Sauvageot O., Carmichael J., Diaz-Latoud C., Arrigo A.P., Rubinsztein D.C. Heat shock protein 27 prevents cellular polyglutamine toxicity and suppresses the increase of reactive oxygen species caused by huntingtin. Hum. Mol. Genet. 11:2002;1137-1151
4. Dabir D.V., Trojanowski J.Q., Richter-Landsberg C., Lee V.M., Forman M.S. Expression of the small heat-shock protein alphaB-crystallin in tauopathies with glial pathology. Am. J. Pathol. 164:2004;155-166
5. Kamradt M.C., Chen F., Sam S., Cryns V.L. The small heat shock protein alpha B-crystallin negatively regulates apoptosis during myogenic differentiation by inhibiting caspase-3 activation. J. Biol. Chem. 277:2002;38731-38736
6. Gober M.D., Smith C.C., Ueda K., Toretsky J.A., Aurelian L. Forced expression of the H11 heat shock protein can be regulated by DNA methylation and trigger apoptosis in human cells. J. Biol. Chem. 278:2003;37600-37609
7. Sun X., Fontaine J.M., Rest J.S., Shelden E.A., Welsh M.J., Benndorf R. Interaction of human HSP22 (HSPB8) with other small heat shock proteins. J. Biol. Chem. 279:2004;2394-2402
8. Evgrafov O.V., Mersiyanova I., Irobi J., Van Den Bosch L., Dierick I., Leung C.L., Schagina O., Verpoorten N., Van Impe K., Fedotov V., et al. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Nat. Genet. 36:2004;602-606
9. Irobi J., Impe K.V., Seeman P., Jordanova A., Dierick I., Verpoorten N., Michalik A., Vriendt E.D., Jacobs A., Gerwen V.V., et al. Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy. Nat. Genet. 36:2004;597-601
10. Depre C., Hase M., Gaussin V., Zajac A., Wang L., Hittinger L., Ghaleh B., Yu X., Kudej R.K., Wagner T., et al. H11 kinase is a novel mediator of myocardial hypertrophy in vivo. Circ. Res. 91:2002;1007-1014
11. Perng M.D., Cairns L., van den I.P., Prescott A., Hutcheson A.M., Quinlan R.A. Intermediate filament interactions can be altered by HSP27 and alphaB-crystallin. J. Cell Sci. 112:1999;2099-2112
12. Quinlan R. Cytoskeletal competence requires protein chaperones. Prog. Mol. Subcell. Biol. 28:2002;219-233
13. Perng M.D., Wen S.F., van den I.P., Prescott A.R., Quinlan R.A. Desmin aggregate formation by R120G {alpha}B-crystallin is caused by altered filament interactions and is dependent upon network status in cells. Mol. Biol. Cell. 15:2004;2335-2346
14. Brownlees J., Ackerley S., Grierson A.J., Jacobsen N.J., Shea K., Anderton B.H., Leigh P.N., Shaw C.E., Miller C.C. Charcot-Marie-Tooth disease neurofilament mutations disrupt neurofilament assembly and axonal transport. Hum. Mol. Genet. 11:2002;2837-2844
15. Helfand B.T., Loomis P., Yoon M., Goldman R.D. Rapid transport of neural intermediate filament protein. J. Cell Sci. 116:2003;2345-2359
16. Weisleder N., Taffet G.E., Capetanaki Y. Bcl-2 overexpression corrects mitochondrial defects and ameliorates inherited desmin null cardiomyopathy. Proc. Natl. Acad. Sci. USA. 101:2004;769-774
17. Libina N., Berman J.R., Kenyon C. Tissue-specific activities of C. elegans DAF16 in the regulation of lifespan. Cell. 115:2003;489-502
18. Mounkes L.C., Kozlov S., Hernandez L., Sullivan T., Stewart C.L. A progeroid syndrome in mice is caused by defects in A-type lamins. Nature. 423:2003;298-301
19. De Sandre-Giovannoli A., Chaouch M., Kozlov S., Vallat J.M., Tazir M., Kassouri N., Szepetowski P., Hammadouche T., Vandenberghe A., Stewart C.L., et al. Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse. Am. J. Hum. Genet. 70:2002;726-736
20. Bai F., Xi J.H., Wawrousek E.F., Fleming T.P., Andley U.P. Hyperproliferation and p53 status of lens epithelial cells derived from aB-crystallin knockout mice. J. Biol. Chem. 278:2003;36876-36886