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LAMP2 as a marker of EBV-mediated B lymphocyte transformation in the study of lysosomal storage diseases

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An Erratum to this article was published on 18 October 2013

Abstract

Following the degradative pathway, vesicles loaded with extracellular material, eventually, dock and fuse with lysosomes, acquiring specific membrane markers of these organelles and acid hydrolases responsible for digest their content. The lysosomal-associated membrane protein 2 (LAMP-2), the best characterized lysosomal membrane protein, is found in late stages of endosome maturation and may be used as a marker of lysosome-associated membranes. Lysosomal storage disorders (LSDs) are described by the absence or deficiency in hydrolase activity leading to substrate accumulation within lysosomal components and to the onset of several diseases. It is known that lymphocytes infected by Epstein–Barr virus (EBV) are able to form cytoplasmic vacuoles, which work as a storage compartment for lysosomal acidic hydrolases. At the present study, we validate the EBV as a transforming agent of B lymphocytes in stability studies of long-term stored samples, since the methods used to keep samples in liquid nitrogen and thaw them have all proven to be efficient in samples frozen for up to 2 years. To confirm and investigate some of the most prevalent LSDs in the South of Brazil—Pompe, Fabry and Gaucher diseases—we first measured the enzymatic activity of α-glicosidase, α-galactosidase, and β-glicosidase in those cytoplasmic-formed vacuoles and then looked to LAMP-2 immunoreactivity by employing confocal microscopy techniques.

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Acknowledgments

The authors are highly grateful to CAPES and CNPq for financial support and to Center for Neuroscience and Cell Biology, University of Coimbra, Portugal.

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Correspondence to A. S. Mello.

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Mello, A.S., Goldim, M.P., Mezzalira, J. et al. LAMP2 as a marker of EBV-mediated B lymphocyte transformation in the study of lysosomal storage diseases. Mol Cell Biochem 385, 1–6 (2014). https://doi.org/10.1007/s11010-013-1806-4

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  • DOI: https://doi.org/10.1007/s11010-013-1806-4

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