X Li 1 , W Pan , G Z Yang , Y N Di , F Zhao , L Y Zhu , Z H Jiang . Show Affiliations »
Abstract
AIM OF THE STUDY: Proteomic approach was applied to identify differential protein expressed in brain of rats with type 1 diabetes mellitus (T1DM) in order to search for potential biomarkers for pathological changes of brain with T1DM. METHODS: Proteins were extracted from brain tissues of T1DM rats and healthy control rats, separated by 2-DE and identified by MALDI-TOF-MS. The results were validated by Western blot analysis and immunohistochemistry (IHC). RESULTS: A total of 8 proteins from the 24 differentially expressed spots were identified by MALDI-TOF-MS. The proteins identified were vitamin D-dependent calcium-binding protein, creatine kinase B-type (B-CK), myosin light chain kinase (MLCK), HSP60 and HSP71, ATP synthase, cyclin-G, pantothenate kinase-1 (PANK1), respectively. 3 proteins were up-regulated and 5 proteins were down-regulated from the T1DM rats. Of the 8 proteins identified, MLCK was confirmed by Western blot and IHC. CONCLUSION: This work demonstrates that a comprehensive strategy of proteomic identification should be a useful tool for understanding of diabetic encephalopathy mechanism. And the differential proteins such as MLCK may be give clues about the pathogenesis of diabetic encephalopathy. © J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York.
AIM OF THE STUDY: Proteomic approach was applied to identify differential protein expressed in brain of rats with type 1 diabetes mellitus (T1DM) in order to search for potential biomarkers for pathological changes of brain with T1DM. METHODS: Proteins were extracted from brain tissues of T1DM rats and healthy control rats , separated by 2-DE and identified by MALDI-TOF-MS. The results were validated by Western blot analysis and immunohistochemistry (IHC). RESULTS: A total of 8 proteins from the 24 differentially expressed spots were identified by MALDI-TOF-MS. The proteins identified were vitamin D -dependent calcium -binding protein, creatine kinase B-type (B-CK), myosin light chain kinase (MLCK ), HSP60 and HSP71, ATP synthase, cyclin-G , pantothenate kinase-1 (PANK1 ), respectively. 3 proteins were up-regulated and 5 proteins were down-regulated from the T1DM rats . Of the 8 proteins identified, MLCK was confirmed by Western blot and IHC. CONCLUSION: This work demonstrates that a comprehensive strategy of proteomic identification should be a useful tool for understanding of diabetic encephalopathy mechanism. And the differential proteins such as MLCK may be give clues about the pathogenesis of diabetic encephalopathy . © J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York.
Entities: Chemical
Disease
Gene
Species
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Year: 2011
PMID: 21472662 DOI: 10.1055/s-0031-1271705
Source DB: PubMed Journal: Exp Clin Endocrinol Diabetes ISSN: 0947-7349 Impact factor: 2.949