Tubers from patients with tuberous sclerosis complex are characterized by changes in microtubule biology through ROCK2 signalling. Issue 3 (29th April 2014)

• Record Type: Journal Article
• Authors: Ferrer, Isidre; Mohan, Pooja; Chen, Helen; Castellsague, Joan; Gómez‐Baldó, Laia; Carmona, Marga; García, Nadia; Aguilar, Helena; Jiang, Jihong; Skowron, Margaretha; Nellist, Mark; Ampuero, Israel; Russi, Antonio; Lázaro, Conxi; Maxwell, Christopher A; Pujana, Miguel Angel
• Is Part Of: Journal of pathology. Volume 233:Issue 3(2014)
• Page Start: 247
• Page End: 257
• Publication Date: 2014-04-29
• Subjects: Pathology -- Periodicals; 616.07
• DOI: 10.1002/path.4343
• Languages: English
• ISSNs: 0022-3417

Abstract

<abstract abstract-type="main" id="path4343-abs-0001"> <title>Abstract</title> <p id="path4343-para-0001">Most patients with tuberous sclerosis complex (TSC) develop cortical tubers that cause severe neurological disabilities. It has been suggested that defects in neuronal differentiation and/or migration underlie the appearance of tubers. However, the precise molecular alterations remain largely unknown. Here, by combining cytological and immunohistochemical analyses of tubers from nine TSC patients (four of them diagnosed with <italic>TSC2</italic> germline mutations), we show that alteration of microtubule biology through ROCK2 signalling contributes to TSC neuropathology. All tubers showed a larger number of binucleated neurons than expected relative to control cortex. An excess of normal and altered cytokinetic figures was also commonly observed. Analysis of centrosomal markers suggested increased microtubule nucleation capacity, which was supported by the analysis of an expression dataset from cortical tubers and control cortex, and subsequently linked to under‐expression of Rho‐associated coiled‐coil containing kinase 2 (ROCK2). Thus, augmented microtubule nucleation capacity was observed in mouse embryonic fibroblasts and human fibroblasts deficient in the <italic>Tsc2/TSC2</italic> gene product, tuberin. Consistent with ROCK2 under‐expression, microtubule acetylation was found to be increased with tuberin deficiency; this alteration was abrogated by rapamycin treatment and mimicked by HDAC6 inhibition. Together, the results of this study support the hypothesis that loss of <italic>TSC2</italic> expression can alter microtubule organization and dynamics, which, in turn, deregulate cell division and potentially impair neuronal differentiation. Copyright © 2014 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd</p> </abstract>