کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10928176 | 1092899 | 2014 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Moesin functionality in hypothermic liver preservation injury
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کلمات کلیدی
FERMSECLPAIPLPKCERMReperfusion injury - آسیب مجددEzrin Radixin Moesin - اذرین رادیسین موزینlysophosphatidic acid - اسید لیسفسفیدیدOrgan donor - اهدا کننده ارگانUniversity of Wisconsin solution - راه حل دانشگاه ویسکانسینRho kinase - رین کینازROK - سالSinusoidal Endothelial Cell - سلول اندوتلیال سینوسPlasma membrane - غشای پلاسماlactate dehydrogenase - لاکتات دهیدروژناز LDH - لاکتات دهیدروژناز به صورت مختصر شده LDH Protein kinase C - پروتئین کیناز سیLiver transplantation - پیوند کبدIsolated perfused liver - کبد پرفیوژن جدا شده
موضوعات مرتبط
علوم زیستی و بیوفناوری
علوم کشاورزی و بیولوژیک
علوم کشاورزی و بیولوژیک (عمومی)
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
The objective of this study was to determine how expression and functionality of the cytoskeletal linker protein moesin is involved in hepatic hypothermic preservation injury. Mouse livers were cold stored in University of Wisconsin (UW) solution and reperfused on an isolated perfused liver (IPL) device for one hour. Human hepatocytes (HepG2) and human or murine sinusoidal endothelial cells (SECs) were cold stored and rewarmed to induce hypothermic preservation injury. The cells were transfected with: wild type moesin, an siRNA duplex specific for moesin, and the moesin mutants T558D and T558A. Tissue and cell moesin expression and its binding to actin were determined by Western blot. Liver IPL functional outcomes deteriorated proportional to the length of cold storage, which correlated with moesin disassociation from the actin cytoskeleton. Cell viability (LDH and WST-8) in the cell models progressively declined with increasing preservation time, which also correlated with moesin disassociation. Transfection of a moesin containing plasmid or an siRNA duplex specific for moesin into HepG2 cells resulted in increased and decreased moesin expression, respectively. Overexpression of moesin protected while moesin knock-down potentiated preservation injury in the HepG2 cell model. Hepatocytes expressing the T558A (inactive) and T558D (active) moesin binding mutants demonstrated significantly more and less preservation injury, respectively. Cold storage time dependently caused hepatocyte detachment from the matrix and cell death, which was prevented by the T558D active moesin mutation. In conclusion, moesin is causally involved in hypothermic liver cell preservation injury through control of its active binding molecular functionality.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cryobiology - Volume 69, Issue 1, August 2014, Pages 34-40
Journal: Cryobiology - Volume 69, Issue 1, August 2014, Pages 34-40
نویسندگان
Tao Tian, Susanne L. Lindell, Chris Kowalski, Martin J. Mangino,