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Sandilands, A.* ; Hutcheson, A.M.* ; Long, H.A.* ; Prescott, A.R.* ; Vrensen, G.* ; Löster, J. ; Klopp, N. ; Lutz, R.B. ; Graw, J. ; Masaki, S.* ; Dobson, C.M.* ; MacPhee, C.E.* ; Quinlan, R.A.*

Altered aggregation properties of mutant gamma-crystallins cause inherited cataract.

EMBO J. 21, 6005-6014 (2002)
Verlagsversion DOI
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Protein inclusions are associated with a diverse group of human diseases ranging from localized neurological disorders through to systemic non-neuropathic diseases. Here, we present evidence that the formation of intranuclear inclusions is a key event in cataract formation involving altered gamma-crystalline that are unlikely to adopt their native fold. In three different inherited murine cataracts involving this type of gamma-crystallin mutation, large inclusions containing the altered gamma-crystalline were found in the nuclei of the primary lens fibre cells. Their formation preceded not only the first gross morphological changes in the lens, but also the first signs of cataract. The inclusions contained filamentous material that could be stained with the amyloid-detecting dye, Congo red. In vitro, recombinant mutant gammaB-crystallin readily formed amyloid fibrils under physiological buffer conditions, unlike wild-type protein. These data suggest that this type of cataract is caused by a mechanism involving the nuclear targeting and deposition of amyloid-like inclusions. The mutant gamma-crystalline initially disrupt nuclear function, but then this progresses to a full cataract phenotype.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter amyloidosis; gamma-crystallins; protein misfolding
ISSN (print) / ISBN 0261-4189
e-ISSN 1460-2075
Zeitschrift EMBO Journal, The
Quellenangaben Band: 21, Heft: 22, Seiten: 6005-6014 Artikelnummer: , Supplement: ,
Verlag Wiley
Verlagsort Heidelberg, Germany
Begutachtungsstatus Peer reviewed