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NDT Advance Access published online on November 12, 2008

Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfn623
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© The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



β2-microglobulin is potentially neurotoxic, but the blood brain barrier is likely to protect the brain from its toxicity

Sofia Giorgetti1, Sara Raimondi1,2, Silvia Cassinelli1,2, Monica Bucciantini3,4, Massimo Stefani3,4, Gina Gregorini5, Giulia Albonico6, Remigio Moratti6, Giovanni Montagna7, Monica Stoppini1,8 and Vittorio Bellotti1,2,8

1 Department of Biochemistry, University of Pavia 2 Laboratori di Biotecnologie, IRCCS Policlinico San Matteo, Pavia 3 Department of Biochemistry and 4 Research Centre on the molecular basis of neurodegeneration (CIMN), University of Florence, Florence 5 Reparto di Nefrologia e Dialisi, Ospedale Civile di Brescia, Brescia 6 Servizio di Analisi Chimico Cliniche, IRCCS Policlinico San Matteo 7 Salvatore Maugeri Foundation, IRCCS, Rehabilitation Institute of Pavia, Division of Nephrology and Haemodialysis, Pavia 8 Consorzio Interuniversitario Istituto Nazionale Biostrutture e Biosistemi (INBB), Roma, Italy

Correspondence and offprint requests to: Vittorio Bellotti, Dipartimento di Biochimica, via Taramelli 3b, 27100 Pavia, Italy. Tel: +39-0382987932; Fax: +39-0382423108; E-mail: vbellot{at}unipv.it



  Abstract

Background. In dialysis-related amyloidosis, β2-microglobulin accumulates as amyloid fibrils preferentially around bones and tendons provoking osteoarthritis. In addition to the pathologic role played by the amyloid fibrils, it can be speculated that a pathogenic role is also played by the high concentrations of soluble β2-microglobulin because it is toxic for certain cell lines like HL60 and mitogen for other cells such as the osteoclasts. The discovery that β2-microglobulin can influence the biology of certain cells may lead to the assumption that it might affect neuronal cells that are quite sensitive to amyloidogenic proteins in the oligomeric state. Such a concern might be supported by clinical evidence that haemodialysis is associated with the risk of a cognitive impairment.

Methods. The cytotoxicity of β2-microglobulin on the SH-SY5Y neuroblastoma cells was assayed by the MTT test. The β2-microglobulin concentration was determined in the cerebrospinal fluid of four different patients by means of immunonephelometry and western blot.

Results. Oligomeric β2-microglobulin is cytotoxic for the SH-SY5Y cells at a concentration that can be easily reached in the plasma of patients on haemodialysis. However, the β2-microglobulin concentration, measured in the cerebrospinal fluid of a haemodialysis patient, appears to be independent of its plasma concentration and is maintained under the lower limit of cytotoxicity we have determined in the cell culture.

Conclusions. Although β2-microglobulin is potentially neurotoxic, it is unlikely that this protein plays a role in the pathophysiology of cognitive impairment observed in haemodialysis patients due to the protective effect of the blood brain barrier that maintains a low concentration of β2-microglobulin in the cerebrospinal fluid.

Keywords: blood brain barrier; cerebrospinal fluid; cytotoxicity; dialysis-related amyloidosis; oligomers

Received for publication: 1. 7.08
Accepted in revised form: 15.10.08


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