کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2190550 1550439 2014 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Proteomic remodeling of proteasome in right heart failure
ترجمه فارسی عنوان
بازسازی پروتئومومی پروتئازوم در نارسایی قلب راست
کلمات کلیدی
پروتئومیک کم. نارسایی قلب راست، پروتئازوم، ابیکتین، فعالیت های پروتئازوم
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
چکیده انگلیسی


• Proteomic analysis was performed on ventricles of right heart failure rat models.
• Analysis reveals that proteasome subunits were decreased in right heart failure.
• Two proteasomal activities were down-regulated in right heart failure.
• These results provide novel insight and therapeutic avenue for right heart failure.

The development of right heart failure (RHF) is characterized by alterations of right ventricle (RV) structure and function, but the mechanisms of RHF remain still unknown. Thus, understanding the RHF is essential for improved therapies. Therefore, identification by quantitative proteomics of targets specific to RHF may have therapeutic benefits to identify novel potential therapeutic targets. The objective of this study was to analyze the molecular mechanisms changing RV function in the diseased RHF and thus, to identify novel potential therapeutic targets. For this, we have performed differential proteomic analysis of whole RV proteins using two experimental rat models of RHF. Differential protein expression was observed for hundred twenty six RV proteins including proteins involved in structural constituent of cytoskeleton, motor activity, structural molecule activity, cytoskeleton protein binding and microtubule binding. Interestingly, further analysis of down-regulated proteins, reveals that both protein and gene expressions of proteasome subunits were drastically decreased in RHF, which was accompanied by an increase of ubiquitinated proteins. Interestingly, the proteasomal activities chymotrypsin and caspase-like were decreased whereas trypsin-like activity was maintained. In conclusion, this study revealed the involvement of ubiquitin–proteasome system (UPS) in RHF. Three deregulated mechanisms were discovered: (1) decreased gene and protein expressions of proteasome subunits, (2) decreased specific activity of proteasome; and (3) a specific accumulation of ubiquitinated proteins. This modulation of UPS of RV may provide a novel therapeutic avenue for restoration of cardiac function in the diseased RHF.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular and Cellular Cardiology - Volume 66, January 2014, Pages 41–52
نویسندگان
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