A1 Refereed original research article in a scientific journal
Alteration of prolyl oligopeptidase and activated alpha-2-macroglobulin in multiple sclerosis subtypes and in the clinically isolated syndrome
Authors: Tenorio-Laranga J, Peltonen I, Keskitalo S, Duran-Torres G, Natarajan R, Mannisto PT, Nurmi A, Vartiainen N, Airas L, Elovaara I, Garcia-Horsman JA
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Publication year: 2013
Journal: Biochemical Pharmacology
Journal name in source: BIOCHEMICAL PHARMACOLOGY
Journal acronym: BIOCHEM PHARMACOL
Number in series: 12
Volume: 85
Issue: 12
First page : 1783
Last page: 1794
Number of pages: 12
ISSN: 0006-2952
DOI: https://doi.org/10.1016/j.bcp.2013.04.018(external)
Abstract
Prolyl oligopeptidase (PREP) has been considered as a drug target for the treatment of neurodegenerative diseases. In plasma, PREP has been found altered in several disorders of the central nervous system including multiple sclerosis (MS). Oxidative stress and the levels of an endogenous plasma PREP inhibitor have been proposed to decrease PREP activity in MS. In this work, we measured the circulating levels of PREP in patients suffering of relapsing remitting (RR), secondary progressive (SP), primary progressive (PP) MS, and in subjects with clinically isolated syndrome (CIS). We found a significantly lower PREP activity in plasma of RRMS as well as in PPMS patients and a trend to reduced activity in subjects diagnosed with CIS, compared to controls. No signs of oxidative inactivation of PREP, and no correlation with the endogenous PREP inhibitor, identified as activated alpha-2-macroglobulin (alpha M-2*), were observed in any of the patients studied. However, a significant decrease of alpha M-2* was recorded in MS. In cell cultures, we found that PREP specifically stimulates immune active cells possibly by modifying the levels of fibrinogen beta, thymosin beta 4, and collagen. Our results open new lines of research on the role of PREP and alpha M-2* in MS, aiming to relate them to the diagnosis and prognosis of this devastating disease. (C) 2013 Elsevier Inc. All rights reserved.
Prolyl oligopeptidase (PREP) has been considered as a drug target for the treatment of neurodegenerative diseases. In plasma, PREP has been found altered in several disorders of the central nervous system including multiple sclerosis (MS). Oxidative stress and the levels of an endogenous plasma PREP inhibitor have been proposed to decrease PREP activity in MS. In this work, we measured the circulating levels of PREP in patients suffering of relapsing remitting (RR), secondary progressive (SP), primary progressive (PP) MS, and in subjects with clinically isolated syndrome (CIS). We found a significantly lower PREP activity in plasma of RRMS as well as in PPMS patients and a trend to reduced activity in subjects diagnosed with CIS, compared to controls. No signs of oxidative inactivation of PREP, and no correlation with the endogenous PREP inhibitor, identified as activated alpha-2-macroglobulin (alpha M-2*), were observed in any of the patients studied. However, a significant decrease of alpha M-2* was recorded in MS. In cell cultures, we found that PREP specifically stimulates immune active cells possibly by modifying the levels of fibrinogen beta, thymosin beta 4, and collagen. Our results open new lines of research on the role of PREP and alpha M-2* in MS, aiming to relate them to the diagnosis and prognosis of this devastating disease. (C) 2013 Elsevier Inc. All rights reserved.
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