Membrane‐type 1 metalloproteinase is upregulated in microglia/brain macrophages in neurodegenerative and neuroinflammatory diseases. Issue 3 (9th December 2013)

• Record Type: Journal Article
• Authors: Langenfurth, Anika; Rinnenthal, Jan Leo; Vinnakota, Katyayni; Prinz, Vincent; Carlo, Anne‐Sophie; Stadelmann, Christine; Siffrin, Volker; Peaschke, Susann; Endres, Matthias; Heppner, Frank; Glass, Rainer; Wolf, Susanne A.; Kettenmann, Helmut
• Is Part Of: Journal of neuroscience research. Volume 92:Issue 3(2014:Mar.)
• Page Start: 275
• Page End: 286
• Publication Date: 2013-12-09
• Subjects: Neurobiology -- Periodicals; 612
• DOI: 10.1002/jnr.23288
• Languages: English
• ISSNs: 0360-4012

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>We previously reported that glioma cells induce the expression of membrane‐type 1 metalloproteinase (MT1‐MMP or MMP‐14) in tumor‐associated microglia/macrophages and promote tumor growth, whereas MMP‐14 expression in microglia under physiological conditions is very low. Here, we show that the increase in MMP‐14 expression is also found in microglia/macrophages associated with neurodegenerative and neuroinflammatory pathologies in mouse models as well as in human biopsies or post‐mortem tissue. We found that microglial/macrophage MMP‐14 expression was upregulated in Alzheimer's disease tissue, in active lesions of multiple sclerosis, and in tissue from stage II stroke as well as in the corresponding mouse models for the human diseases. In contrast, we observed no upregulation for MMP‐14 in microglia/macrophages in the early phase of stroke or in the corresponding mouse model, in human amyotrophic lateral sclerosis (ALS) tissue or in a mouse model of ALS as well as in human cases of acute brain trauma. These data indicate that MMP‐14 expression is not a general marker for activated microglia/macrophages but is upregulated in defined stages of neuroinflammatory and neurodegenerative diseases and that there is generally a good match between mouse models and human brain pathologies. © 2013 Wiley Periodicals, Inc.</p> </abstract>