@article {Bruinsma11992, author = {Ilona B. Bruinsma and Mieke de Jager and Anna Carrano and Alexandra A. M. Versleijen and Robert Veerhuis and Wilbert Boelens and Annemieke J. M. Rozemuller and Robert M. W. de Waal and Marcel M. Verbeek}, title = {Small Heat Shock Proteins Induce a Cerebral Inflammatory Reaction}, volume = {31}, number = {33}, pages = {11992--12000}, year = {2011}, doi = {10.1523/JNEUROSCI.0945-11.2011}, publisher = {Society for Neuroscience}, abstract = {More than 80\% of Alzheimer{\textquoteright}s disease (AD) patients have some degree of cerebral amyloid angiopathy (CAA). In addition to arteries and veins, capillaries can also be affected. Capillary CAA (capCAA), rather than CAA in larger vessels, is associated with flame-like amyloid-beta (Aβ) deposits that may extend beyond the vessel wall and radiate into the neuropil, a phenomenon also known as {\textquotedblleft}dyshoric angiopathy.{\textquotedblright} Aβ deposits in AD, parenchymal as well as (cap)CAA and dyshoric angiopathy, are associated with a local inflammatory reaction, including activation of microglial cells and astrocytes that, among others, produce cytokines and reactive oxygen species. This neuroinflammatory reaction may account for at least part of the cognitive decline. In previous studies we observed that small heat shock proteins (sHsps) are associated with Aβ deposits in AD. In this study the molecular chaperones Hsp20, HspB8 and HspB2B3 were found to colocalize with CAA and capCAA in AD brains. In addition, Hsp20, HspB8 and HspB2B3 colocalized with intercellular adhesion molecule 1 (ICAM-1) in capCAA-associated dyshoric angiopathy. Furthermore, we demonstrated that Hsp20, HspB8 and HspB2B3 induced production of interleukin 8, soluble ICAM-1 and monocyte chemoattractant protein 1 by human leptomeningeal smooth muscle cells and human brain astrocytes in vitro and that Hsp27 inhibited production of transforming growth factor beta 1 and CD40 ligand. Our results suggest a central role for sHsps in the neuroinflammatory reaction in AD and CAA and thus in contributing to cognitive decline.}, issn = {0270-6474}, URL = {https://www.jneurosci.org/content/31/33/11992}, eprint = {https://www.jneurosci.org/content/31/33/11992.full.pdf}, journal = {Journal of Neuroscience} }