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Statins reduce human blood–brain barrier permeability and restrict leukocyte migration: Relevance to multiple sclerosis
Author(s) -
Ifergan Igal,
Wosik Karolina,
Cayrol Romain,
Kébir Hania,
Auger Chantale,
Bernard Monique,
Bouthillier Alain,
Moumdjian Robert,
Duquette Pierre,
Prat Alexandre
Publication year - 2006
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.20875
Subject(s) - lovastatin , occludin , blood–brain barrier , multiple sclerosis , simvastatin , tight junction , chemokine , hmg coa reductase , pharmacology , central nervous system , immunology , inflammation , medicine , biology , chemistry , endocrinology , microbiology and biotechnology , reductase , biochemistry , cholesterol , enzyme
Objective Dysregulation of the blood–brain barrier (BBB) and transendothelial migration of immune cells are among the earliest central nervous system changes partaking in lesion formation in both multiple sclerosis (MS) and its early clinical form, the clinically isolated syndrome. Evidence for the anti‐inflammatory effects of 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase inhibitors within the central nervous system arose from studies demonstrating that statins improve clinical signs in the animal model of MS and reduce the number of gadolinium‐enhancing lesions in MS. Methods We sought to describe the impact of 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase inhibitor treatment on the physiology and immunology of human BBB‐derived endothelial cells (ECs). Results We demonstrate that lovastatin and simvastatin induce a 50 to 60% reduction in the diffusion rates of bovine serum albumin and [ 14 C]‐sucrose across human BBB‐ECs in vitro through abrogation of isoprenylation processes, but independent of the expression of the tight junction molecules occludin, VE‐cadherin, JAM‐1, zonula occluden‐1, and zonula occluden‐2. Simvastatin and lovastatin were equipotent in reducing BBB permeability in vitro, with median effective concentration (EC 50 ) of 9.5 × 10 −8 and 1.0 × 10 −7 M, respectively. We further demonstrate that lovastatin and simvastatin treatment of BBB‐ECs significantly restricts the migration of clinically isolated syndrome–derived and MS‐derived monocytes and lymphocytes across the human BBB in vitro, through a specific reduction in the secretion of the chemokines monocyte chemotactic protein‐1/CCL2 and interferon‐γ–inducible protein‐10/CXCL10 by BBB‐ECs. Interpretation Our data parallel the previously reported magnetic resonance imaging–based radiological findings and suggest an effect of statins that could be beneficial in early MS, restricting the diffusion of molecular tracers and the migration of immune cells across the human BBB. Ann Neurol 2006