中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
2期
199-204
,共6页
赵爱超%马依彤%姚永钊%曹雯%于海滨%余辉%刘芬%陈邦党%马翔
趙愛超%馬依彤%姚永釗%曹雯%于海濱%餘輝%劉芬%陳邦黨%馬翔
조애초%마의동%요영쇠%조문%우해빈%여휘%류분%진방당%마상
组织构建%组织工程%细胞周期素A2%乳鼠%心肌细胞%细胞周期%定位%增殖细胞核抗原%调控%国家自然科学基金
組織構建%組織工程%細胞週期素A2%乳鼠%心肌細胞%細胞週期%定位%增殖細胞覈抗原%調控%國傢自然科學基金
조직구건%조직공정%세포주기소A2%유서%심기세포%세포주기%정위%증식세포핵항원%조공%국가자연과학기금
cyclins%cyclin A%cyclin A2%myocytes,cardiac%proliferating cell nuclear antigen
背景:细胞周期素A2是调节细胞周期的关键因子,关于细胞周期素A2在乳鼠心肌中的表达及定位情况还不明确。<br> 目的:探索细胞周期素A2在C57乳鼠中的表达定位及表达,检测心肌细胞中增殖相关蛋白随着细胞周期素A2的表达而呈现的表达趋势。<br> 方法:C57乳鼠分别于出生后0,3,7,14,28 d处死,留取心肌组织,行Western blot检测心肌组织中细胞周期素A2、增殖细胞核抗原及磷酸组蛋白H3的表达情况。免疫组化检测细胞周期素A2在出生后乳鼠中的定位及增殖细胞核抗原在心肌组织中的表达。<br> 结果与结论:C57乳鼠出生后细胞周期素A2表达水平逐渐下调,直至第14天基本消失(P=0.001),且细胞周期素A2在乳鼠出生后0 d定位于细胞核中,在第14天时主要存在于细胞质中,至第28天时,基本消失。增殖细胞核抗原在出生后0 d表达最强,随后表达逐渐减弱。而反映有丝分裂期的特异性蛋白磷酸组蛋白H3随时间表达逐渐减少,且表达强度基本与细胞周期素A2表达减弱相一致。
揹景:細胞週期素A2是調節細胞週期的關鍵因子,關于細胞週期素A2在乳鼠心肌中的錶達及定位情況還不明確。<br> 目的:探索細胞週期素A2在C57乳鼠中的錶達定位及錶達,檢測心肌細胞中增殖相關蛋白隨著細胞週期素A2的錶達而呈現的錶達趨勢。<br> 方法:C57乳鼠分彆于齣生後0,3,7,14,28 d處死,留取心肌組織,行Western blot檢測心肌組織中細胞週期素A2、增殖細胞覈抗原及燐痠組蛋白H3的錶達情況。免疫組化檢測細胞週期素A2在齣生後乳鼠中的定位及增殖細胞覈抗原在心肌組織中的錶達。<br> 結果與結論:C57乳鼠齣生後細胞週期素A2錶達水平逐漸下調,直至第14天基本消失(P=0.001),且細胞週期素A2在乳鼠齣生後0 d定位于細胞覈中,在第14天時主要存在于細胞質中,至第28天時,基本消失。增殖細胞覈抗原在齣生後0 d錶達最彊,隨後錶達逐漸減弱。而反映有絲分裂期的特異性蛋白燐痠組蛋白H3隨時間錶達逐漸減少,且錶達彊度基本與細胞週期素A2錶達減弱相一緻。
배경:세포주기소A2시조절세포주기적관건인자,관우세포주기소A2재유서심기중적표체급정위정황환불명학。<br> 목적:탐색세포주기소A2재C57유서중적표체정위급표체,검측심기세포중증식상관단백수착세포주기소A2적표체이정현적표체추세。<br> 방법:C57유서분별우출생후0,3,7,14,28 d처사,류취심기조직,행Western blot검측심기조직중세포주기소A2、증식세포핵항원급린산조단백H3적표체정황。면역조화검측세포주기소A2재출생후유서중적정위급증식세포핵항원재심기조직중적표체。<br> 결과여결론:C57유서출생후세포주기소A2표체수평축점하조,직지제14천기본소실(P=0.001),차세포주기소A2재유서출생후0 d정위우세포핵중,재제14천시주요존재우세포질중,지제28천시,기본소실。증식세포핵항원재출생후0 d표체최강,수후표체축점감약。이반영유사분렬기적특이성단백린산조단백H3수시간표체축점감소,차표체강도기본여세포주기소A2표체감약상일치。
BACKGROUND:Cyclin A2 is a key regulator of cellcycle. Location and expression of cyclin A2 in neonatal mouse myocardium is not clear. <br> OBJECTIVE:To observe the location and expression of cyclin A2 in neonatal mouse cardiomyocytes and its relationship with the exit of cardiomyocytes from cellcycle. <br> METHODS:Neonatal mice were kil ed to take myocardial tissues at 0, 3, 7, 14 and 28 days after birth. Western blot were used to detect the expression of cyclin A2, proliferating cellnucleus antigen and Phospho-histone H3. Immunohistochemitry detection was used to detect the location of cyclin A2 and expression of proliferation cellnucleus antigen at different time after birth. <br> RESULTS AND CONCLUSION:Western blot showed the decrease of cyclin A2 after birth til disappeared at day 4 (P=0.001). Cyclin A2 located mainly in the nucleus after birth and exported to the cytoplasm at day 14, and basical y disappeared at day 28. Proliferating cellnucleus antigen showed gradual y decreased tendency after birth. Mitosis specific marker, Phospho-histone H3, exhibited a gradual decrease after birth, which was consistent with cyclin A2 in expression intensity.