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Light Chain Amyloid Fibrils Cause Metabolic Dysfunction in Human Cardiomyocytes.
PLoS One. 2015 Sep 22;10(9):e0137716. doi: 10.1371/journal.pone.0137716
McWilliams-Koeppen HP, Foster JS, Hackenbrack N, Ramirez-Alvarado M, Donohoe D, Williams A, Macy S, Wooliver C, Wortham D, Morrell-Falvey J, Foster CM, Kennel SJ, Wall JS
Abstract:
.....We have studied the effects of (light chain) amyloid fibrils, produced from recombinant λ6 light chain variable domains, on metabolic activity of human cardiomyocytes. The data indicate that fibrils at 0.1 μM, but not monomer, significantly decrease the enzymatic activity of cellular NAD(P)H-dependent oxidoreductase, without causing significant cell death. The presence of amyloid fibrils did not affect ATP levels; however, oxygen consumption was increased and reactive oxygen species were detected. Confocal fluorescence microscopy showed that fibrils bound to and remained at the cell surface with little fibril internalization. These data indicate that AL amyloid fibrils severely impair cardiomyocyte metabolism in a dose dependent manner. These data suggest that effective therapeutic intervention for these patients should include methods for removing potentially toxic amyloid fibrils.
PMID: 26393799
Free Full-Text: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579077/
Tags: AL amyloidosis, cell culture, heart