Document Detail


Cytoplasmic accumulation of TDP-43 in circulating lymphomonocytes of ALS patients with and without TARDBP mutations.
MedLine Citation:
PMID:  21120508     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
TDP-43, encoded by TARDBP, is a ubiquitously expressed, primarily nuclear protein. In recent years, TDP-43 has been identified as the major pathological protein in ALS due to its mislocalisation in the cytoplasm of motor neurons of patients with and without TARDBP mutations and expression in forms that do not match its predicted molecular weight. In this study, the TDP-43 profile was investigated using western immunoblot analysis in whole lysates, nuclei and cytoplasm of circulating lymphomonocytes from 16 ALS patients, 4 with (ALS/TDP+) and 12 without (ALS/TDP-) TARDBP mutations in the protein C-terminal domain, and thirteen age-matched, healthy donors (controls). Three disease-unaffected first-degree relatives of an ALS/TDP+ patient were also included: one carried the parent mutation (Rel/TDP+) whereas the other two did not (Rel/TDP-). In all ALS patients, relatives and controls, TDP-43 retained the predicted molecular weight in whole cell lysates and nuclei, but in the cytoplasm its molecular weight was slightly smaller than expected. In quantitative terms, TDP-43 was expressed at approximately the same levels in whole cell lysates of ALS patients, relatives and controls. In contrast, TDP-43 accumulated in the cytoplasm with concomitant nuclear depletion in all ALS/TDP+ patients, in about 50% of ALS/TDP- patients and in the Rel/TDP+ subject compared to the controls. In the remaining ALS/TDP- patients and in the two Rel/TDP- subjects, TDP-43 matched the control levels in both subcellular compartments. Were these findings further confirmed, circulating lymphomonocytes could be informative of TDP-43 mislocalisation in nervous tissue and used as a biomarker for future disease risk.
Authors:
Giovanni De Marco; Elisa Lupino; Andrea Calvo; Cristina Moglia; Barbara Buccinnà; Silvia Grifoni; Cristina Ramondetti; Annarosa Lomartire; Maria Teresa Rinaudo; Marco Piccinini; Maria Teresa Giordana; Adriano Chiò
Related Documents :
12585368 - Correlation of the density of yeast malassezia with the clinical severity of seborrhoei...
8272228 - Skin surface ph, moisture, and pruritus in haemodialysis patients.
132088 - Cutaneous reactions to propranolol (inderal).
19515078 - Somatostatin receptor scintigraphy in primary cutaneous t- and b-cell lymphomas.
9461138 - Changes in charges and costs associated with hospitalization of patients with mandibula...
22736088 - Active inflammation and structural change in early active axial spondyloarthritis as de...
Publication Detail:
Type:  Journal Article     Date:  2010-12-01
Journal Detail:
Title:  Acta neuropathologica     Volume:  121     ISSN:  1432-0533     ISO Abbreviation:  Acta Neuropathol.     Publication Date:  2011 May 
Date Detail:
Created Date:  2011-05-02     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0412041     Medline TA:  Acta Neuropathol     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  611-22     Citation Subset:  IM    
Affiliation:
Department of Medicine and Experimental Oncology, Section of Biochemistry, University of Turin, Via Michelangelo n 27b, 10126, Turin, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Pediatric intramedullary cavernous malformation of the conus medullaris: case report and review of t...
Next Document:  Blood-derived iron mediates free radical production and neuronal death in the hippocampal CA1 area f...