エンドプラズマ網膜のストレスと代謝疾患の炎症的基礎
1Department of Genetics and Complex Diseases, Broad Institute of Harvard and MIT, Harvard School of Public Health, Boston, MA 02115, USA. ghotamis@hsph.harvard.edu
Cell
|March 23, 2010
まとめ
エンドプラズマ網膜 (ER) は,タンパク質の折り畳みに不可欠です. その機能障害は,展開されたタンパク質応答 (UPR) を誘発し,細胞ストレスを肥満や糖尿病のような炎症性および代謝疾患と結びつける.
科学分野:
- 細胞生物学 細胞生物学
- 分子生物学は分子生物学である.
- メタボリック疾患の研究
背景:
- エンドプラズマ網膜 (ER) は,タンパク質の合成,折り畳み,輸送に不可欠な器官である.
- 細胞のストレスはERの容量を圧倒し,展開されたタンパク質応答 (UPR) に繋がります.
研究 の 目的:
- 慢性代謝疾患の文脈におけるERストレスとUPRの役割を調査する.
- ERシグナル伝達,炎症,代謝機能障害の交差点を調査する.
主な方法:
- この研究は,細胞生物学と分子信号伝達経路からの知識を統合しています.
- ERストレス,UPR,炎症,代謝疾患に関する既存の文献の分析.
主要な成果:
- ERストレスとUPRの活性化は,炎症とストレスのシグナル伝達経路と関連しています.
- これらの経路は,肥満,インスリン抵抗性,および2型糖尿病の病原性に関与しています.
結論:
- ERとその関連信号ネットワークは,炎症と代謝疾患の重要なネクサスです.
- ER機能をターゲットにすることで,代謝障害に対する新しい治療戦略を提供することができる.
関連する概念動画
Role of ER in the Secretory Pathway
Eukaryotic cells have a special pathway that enables communication between various intracellular membrane-bound compartments and also with the extracellular environment. This pathway is termed as the secretory pathway.
Components of the secretory pathway
About a third of proteins synthesized in the cell are sorted via the secretory route. They shuffle between different compartments in membrane-bound vesicles until they reach their final destination. The main intracellular compartments involved...
Components of the secretory pathway
About a third of proteins synthesized in the cell are sorted via the secretory route. They shuffle between different compartments in membrane-bound vesicles until they reach their final destination. The main intracellular compartments involved...
Regulation of the Unfolded Protein Response
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
The Unfolded Protein Response
The ER is the hub of protein synthesis in a cell. It has robust systems to quality control protein folding and also for degradation of terminally misfolded proteins. Under normal conditions, a small proportion of misfolded proteins that cannot be salvaged need to be transported to the cytoplasm by the ER-associated degradation or ERAD pathways. However, if the ERAD cannot handle the misfolded proteins, the cell activates the unfolded protein response or UPR to adjust the protein folding...
Smooth Endoplasmic Reticulum
Smooth endoplasmic reticulum or smooth ER is a sub-organelle with specialized functions in animal cells and plant cells. It is often associated with the tubule morphology of the endoplasmic reticulum.
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
Type II Diabetes II: Pathophysiology
PathophysiologyType 2 diabetes mellitus (T2DM ) is a chronic metabolic disorder characterized by insulin resistance and progressive pancreatic β-cell dysfunction, leading to impaired glucose homeostasis. It results from interactions among genetic predisposition, environmental factors, and metabolic stressors, such as overnutrition and a sedentary lifestyle.Insulin Resistance and Glucose DysregulationEarly T2DM involves insulin resistance in skeletal muscle, adipose tissue, and the liver.
Post-translational Translocation of Proteins to the RER
A sizable fraction of proteins destined for ER are first synthesized in the cell cytosol and then transported across the ER membrane–a process called post-translational translocation. Similar to cotranslationally translocated proteins, these proteins also use the Sec translocon complex to enter the ER lumen.
Targeting proteins to the ER
Hsp40 and Hsp70 chaperone molecules bind the translated proteins in the cytosol to prevent their folding. The chaperone binding helps to keep the signal...
Targeting proteins to the ER
Hsp40 and Hsp70 chaperone molecules bind the translated proteins in the cytosol to prevent their folding. The chaperone binding helps to keep the signal...
