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Title: Prefibrillar transthyretin oligomers and cold stored native tetrameric transthyretin are cytotoxic in cell culture

Journal Article · · Biochemical and Biophysical Research Communications
;  [1];  [2];  [3];  [1]
  1. IFM- Department of Chemistry, Linkoeping University, SE-581 83 Linkoeping (Sweden)
  2. Department of Physics, Norwegian University of Science and Technology, 7491 Trondheim (Norway)
  3. Division of Experimental Pathology, Faculty of Health Sciences, Linkoeping University, S-581 85 Linkoeping (Sweden)

Recent studies suggest that soluble, oligomeric species, which are intermediates in the fibril formation process in amyloid disease, might be the key species in amyloid pathogenesis. Soluble oligomers of human wild type transthyretin (TTR) were produced to elucidate oligomer properties. Employing ThT fluorescence, time-resolved fluorescence anisotropy of pyrene-labeled TTR, chemical cross-linking, and electron microscopy we demonstrated that early formed soluble oligomers (within minutes) from A-state TTR comprised on the average 20-30 TTR monomers. When administered to neuroblastoma cells these early oligomers proved highly cytotoxic and induced apoptosis after 48 h of incubation. More mature fibrils (>24 h of fibrillation) were non-toxic. Surprisingly, we also found that native tetrameric TTR, when purified and stored under cold conditions (4 deg. C) was highly cytotoxic. The effect could be partially restored by increasing the temperature of the protein. The cytotoxic effects of native tetrameric TTR likely stems from a hitherto unexplored low temperature induced rearrangement of the tetramer conformation that possibly is related to the conformation of misfolded TTR in amyloigogenic oligomers.

OSTI ID:
21255803
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 377, Issue 4; Other Information: DOI: 10.1016/j.bbrc.2008.10.121; PII: S0006-291X(08)02081-0; Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English