Heat shock proteins: cellular and molecular mechanisms in the central nervous system

RA Stetler, Y Gan, W Zhang, AK Liou, Y Gao… - Progress in …, 2010 - Elsevier
Emerging evidence indicates that heat shock proteins (HSPs) are critical regulators in
normal neural physiological function as well as in cell stress responses. The functions of …

Insights on human small heat shock proteins and their alterations in diseases

B Tedesco, R Cristofani, V Ferrari, M Cozzi… - Frontiers in molecular …, 2022 - frontiersin.org
The family of the human small Heat Shock Proteins (HSPBs) consists of ten members of
chaperones (HSPB1-HSPB10), characterized by a low molecular weight and capable of …

Heat shock proteins 70 and 90 inhibit early stages of amyloid β-(1–42) aggregation in vitro

CG Evans, S Wisén, JE Gestwicki - Journal of Biological Chemistry, 2006 - ASBMB
Alzheimer disease is a neurological disorder that is characterized by the presence of fibrils
and oligomers composed of the amyloid β (Aβ) peptide. In models of Alzheimer disease …

Molecular mechanisms for Alzheimer's disease: implications for neuroimaging and therapeutics

CL Masters, R Cappai, KJ Barnham… - Journal of …, 2006 - Wiley Online Library
Alzheimer's disease is a progressive neurodegenerative disorder characterised by the
gradual onset of dementia. The pathological hallmarks of the disease are β‐amyloid (Aβ) …

Identification of the key structural motifs involved in HspB8/HspB6–Bag3 interaction

M Fuchs, DJ Poirier, SJ Seguin, H Lambert… - Biochemical …, 2010 - portlandpress.com
The molecular chaperone HspB8 [Hsp (heat-shock protein) B8] is member of the B-group of
Hsps. These proteins bind to unfolded or misfolded proteins and protect them from …

Modulation of amyloid states by molecular chaperones

A Wentink… - Cold Spring Harbor …, 2019 - cshperspectives.cshlp.org
Aberrant protein aggregation is a defining feature of most neurodegenerative diseases.
During pathological aggregation, key proteins transition from their native state to alternative …

[HTML][HTML] The interaction of αB-crystallin with mature α-synuclein amyloid fibrils inhibits their elongation

CA Waudby, TPJ Knowles, GL Devlin, JN Skepper… - Biophysical journal, 2010 - cell.com
Abstract αB-Crystallin is a small heat-shock protein (sHsp) that is colocalized with α-
synuclein (αSyn) in Lewy bodies—the pathological hallmarks of Parkinson's disease—and …

Suppression of in vivo β-amyloid peptide toxicity by overexpression of the HSP-16.2 small chaperone protein

V Fonte, DR Kipp, J Yerg, D Merin, M Forrestal… - Journal of Biological …, 2008 - ASBMB
Expression of the human β-amyloid peptide (Aβ) in a transgenic Caenorhabditis elegans
Alzheimer disease model leads to the induction of HSP-16 proteins, a family of small heat …

Amyloid β-protein assembly as a therapeutic target of Alzheimer's disease

G Yamin, K Ono, M Inayathullah… - Current pharmaceutical …, 2008 - ingentaconnect.com
Alzheimer's disease (AD), the most common neurodegenerative disorder in the aged, is
characterized by the cerebral deposition of fibrils formed by the amyloid β-protein (Aβ), a 40 …

Could heat therapy be an effective treatment for Alzheimer's and Parkinson's diseases? A narrative review

AP Hunt, GM Minett, OR Gibson, GK Kerr… - Frontiers in …, 2020 - frontiersin.org
Neurodegenerative diseases involve the progressive deterioration of structures within the
central nervous system responsible for motor control, cognition, and autonomic function …