医学研究与教育
醫學研究與教育
의학연구여교육
MEDICAL RESEARCH AND EDUCATION
2014年
3期
76-81
,共6页
张珂%陈鹊汀%王晓冬%张越%李婷婷%石林
張珂%陳鵲汀%王曉鼕%張越%李婷婷%石林
장가%진작정%왕효동%장월%리정정%석림
内皮素%受体%分布%生物功能
內皮素%受體%分佈%生物功能
내피소%수체%분포%생물공능
endothelin%receptors%distribution%biological function
内皮素(Endothelin, ET)是一种由21个氨基酸组成的生物活性物质。它主要由内皮细胞合成,具有非常强烈的收缩血管的生物活性。近年来研究发现除了具有强烈缩血管作用,同时内皮素也具有诱导血管生成、促分化、促细胞有丝分裂和类细胞生长因子的性质。研究文献发现人有3种内皮素亚型(ET-1、ET-2、ET-3),这三个异构肽的生物活性有一定差异,ET-1的作用最强,ET-3最弱。内皮素分子通过内皮素受体(ETRs)发挥其生理和病理作用。内皮素受体被发现广泛地表达于动物的心血管系统、神经系统和胃肠道之中。内皮素受体A(ETA)和内皮素受体B(ETB)有共同的信号转导通路。同时,ETB激活后还能促进PLA2激活。研究还发现内皮素与良恶性肿瘤有广泛的联系。
內皮素(Endothelin, ET)是一種由21箇氨基痠組成的生物活性物質。它主要由內皮細胞閤成,具有非常彊烈的收縮血管的生物活性。近年來研究髮現除瞭具有彊烈縮血管作用,同時內皮素也具有誘導血管生成、促分化、促細胞有絲分裂和類細胞生長因子的性質。研究文獻髮現人有3種內皮素亞型(ET-1、ET-2、ET-3),這三箇異構肽的生物活性有一定差異,ET-1的作用最彊,ET-3最弱。內皮素分子通過內皮素受體(ETRs)髮揮其生理和病理作用。內皮素受體被髮現廣汎地錶達于動物的心血管繫統、神經繫統和胃腸道之中。內皮素受體A(ETA)和內皮素受體B(ETB)有共同的信號轉導通路。同時,ETB激活後還能促進PLA2激活。研究還髮現內皮素與良噁性腫瘤有廣汎的聯繫。
내피소(Endothelin, ET)시일충유21개안기산조성적생물활성물질。타주요유내피세포합성,구유비상강렬적수축혈관적생물활성。근년래연구발현제료구유강렬축혈관작용,동시내피소야구유유도혈관생성、촉분화、촉세포유사분렬화류세포생장인자적성질。연구문헌발현인유3충내피소아형(ET-1、ET-2、ET-3),저삼개이구태적생물활성유일정차이,ET-1적작용최강,ET-3최약。내피소분자통과내피소수체(ETRs)발휘기생리화병리작용。내피소수체피발현엄범지표체우동물적심혈관계통、신경계통화위장도지중。내피소수체A(ETA)화내피소수체B(ETB)유공동적신호전도통로。동시,ETB격활후환능촉진PLA2격활。연구환발현내피소여량악성종류유엄범적련계。
Endothelins (ETs) are composed of 21-aminoacids produced by endothelial cells and considered to be potent vasoconstrictor. Recent studies found that they could not only induce the angiogenesis, mitosis and differentiation, but also act the role of cytokines. Previous studies have identiifed three isoforms of ET (ET-1, ET-2 and ET-3), which are involved in a variety of physiological and pathological processes. ET-1 is most potent one among ETs, whereas ET-3 is the weakest once. ET peptides exhibit their functions in a number of mammalian physiological systems, including gastrointestinal. ETs act via two distinct isoforms of receptors in human body, i.e. endothelin receptor A (ETA) and endothelin receptor B (ETB), which can be found expressed in many mammalian cardiovascular system, neural system and gastrointestinal tract. ETA and ETB have same signaling pathways. And at the meantime, ETB can promote the activation of PLA2. The study also found that endothelins were widely associated with benign and malignant diseases.