Expression profiles of RNA‐Seq‐based grey matter‐specific genes versus white matter‐specific genes in grey matter lesions of multiple sclerosis. Issue 3 (23rd May 2015)

• Record Type: Journal Article
• Authors: Satoh, Jun‐ichi; Kino, Yoshihiro
• Is Part Of: Clinical & experimental neuroimmunology. Volume 6:Issue 3(2015)
• Page Start: 289
• Page End: 298
• Publication Date: 2015-05-23
• Subjects: 616.80479
• DOI: 10.1111/cen3.12218
• Languages: English
• ISSNs: 1759-1961

Abstract

<abstract abstract-type="main" id="cen312218-abs-0001"> <title>Abstract</title> <sec id="cen312218-sec-0001" sec-type="section"> <title>Objectives</title> <p>Accumulating evidence shows that formation of cortical grey matter lesions, characterized by accumulation of activated microglia, axonal transection, synaptic loss and neuronal apoptosis, is common in multiple sclerosis (MS) beginning at the early stage. Grey matter lesions are closely associated with disease progression and permanent disability in MS. At present, the precise molecular signature characteristic of grey matter damage in MS brains remains to be intensively characterized.</p> </sec> <sec id="cen312218-sec-0002" sec-type="section"> <title>Methods</title> <p>To elucidate this, we identified grey matter‐specific genes (GMSG) and white matter‐specific genes (WMSG) abundantly expressed in the normal human brain by analyzing a RNA‐Seq dataset numbered SRP033291, composed of the comprehensive transcriptome of separated grey matter and white matter samples. Then, we studied expression profiles of GMSG and WMSG in MS lesions by analyzing microarray datasets derived from representative cases of grey matter lesions and white matter lesions.</p> </sec> <sec id="cen312218-sec-0003" sec-type="section"> <title>Results</title> <p>We identified 714 RNA‐Seq‐based GMSG closely related to neuronal functions and 378 WMSG with relevance to glial functions. Numerous WMSG, such as KLK6, GJB1 and MYRF, were downregulated in both grey matter and white matter lesions, whereas the expression of various GMSG, such as PVALB, NEUROD6 and LINGO1, was reduced exclusively in grey matter lesions.</p> </sec> <sec id="cen312218-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Grey matter lesions of MS are characterized by underexpression of grey matter components, and the panel of RNA‐Seq‐based GMSG and WMSG serves as molecular markers for discrimination between grey matter and white matter lesions of MS.</p> </sec> </abstract>