The small heat-shock proteins : cellular functions and mutations causing neurodegenerationThe small heat-shock proteins : cellular functions and mutations causing neurodegeneration
Faculty of Pharmaceutical, Biomedical and Veterinary Sciences . Biomedical Sciences
VIB DMG - Peripheral Neuropathies Group
Berlin :Springer, 2011[*]2011
Folding for the synapse / Wyttensbach, A. [edit.]; et al. [edit.]
University of Antwerp
Small heat-shock proteins (small Hsps) are a family of highly conserved proteins involved in multiple cellular mechanisms. Apart from their central role as chaperones in protecting cells during stressful conditions (as outlined in the previous two chapters), small Hsps also function to maintain cellular homeostasisin physiological conditions. Correct protein refolding to avoid aggregation, targeting misfolded proteins for degradation, proper cytoskeletal organization, and anti-apoptotic functions are some of the extensively studied attributes of small Hsps. One or more of these cellular mechanisms may malfunction in specific sets of neurons leading to neurodegenerative diseases such as Alzheimers disease, Parkinsons disease, polyglutamine disorders, and amyotrophic lateral sclerosis. Many in vitro models of these diseases have demonstrated the beneficial roles of small Hsps pointing out their protective role in attenuating the neurodegenerative phenotype. Interestingly, mutations in small Hsps themselves were linked to other degenerative disorders like inherited peripheral neuropathies and familial myopathies. Although not much is known regarding the exact patho-mechanism (loss of function or gain of function) of mutations in causing disease, these discoveries reiterate the importance of small Hsps in maintaining neuronal health and indicate that the small Hsp family of proteins might have more functions than meets the eye. This chapter reviews the current knowledge regarding these enigmatic proteins, including their structure and function and how mutations in these once forgotten proteins might alter their functions and cause neurodegeneration.