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Title

Protein degradation in a LAMP-2-deficient B-lymphoblastoid cell line from a patient with Danon disease

AuthorsSánchez-Lanzas, Raul; Álvarez-Castelao, Beatriz; Castaño, José G.
KeywordsAlpha-synuclein
Chaperone-mediated autophagy
Rcan1
Glyceraldehyde-3-phosphate dehydrogenase
IkappaB
Danon disease
LAMP-2
Autophagy
Ubiquitin proteasome
Issue Date2016
PublisherElsevier
CitationBBA - Molecular Basis of Disease 1862(8): 1423-1432 (2016)
AbstractDanon disease, a condition characterized by cardiomyopathy, myopathy, and intellectual disability, is caused by mutations in the LAMP-2 gene. Lamp-2A protein, generated by alternative splicing from the Lamp-2 pre-mRNA, is reported to be the lysosomal membrane receptor essential for the chaperone-mediated autophagic pathway (CMA) aimed to selective protein targeting and translocation into the lysosomal lumen for degradation. To study the relevance of Lamp-2 in protein degradation, a lymphoblastoid cell line was obtained by EBV transformation of B-cells from a Danon patient. The derived cell line showed no significant expression of Lamp-2 protein. The steady-state mRNA and protein levels of alpha-synuclein, IΚBα, Rcan1, and glyceraldehyde-3-phosphate dehydrogenase, four proteins reported to be selective substrates of the CMA pathway, were similar in control and Lamp-2-deficient cells. Inhibition of protein synthesis showed that the half-life of alpha-synuclein, IΚBα, and Rcan1 was similar in control and Lamp-2-deficient cells, and its degradation prevented by proteasome inhibitors. Both in control and Lamp-2-deficient cells, induction of CMA and macroautophagy by serum and aminoacid starvation of cells for 8 h produced a similar decrease in IΚBα and Rcan1 protein levels and was prevented by the addition of lysosome and autophagy inhibitors. In conclusion, the results presented here showed that Lamp-2 deficiency in human lymphoblastoid cells did not modify the steady-state levels or the degradation of several protein substrates reported as selective substrates of the CMA pathway.
URIhttp://hdl.handle.net/10261/150933
DOI10.1016/j.bbadis.2016.04.014
Identifiersdoi: 10.1016/j.bbadis.2016.04.014
issn: 0925-4439
Appears in Collections:(IIBM) Artículos
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