解剖学杂志
解剖學雜誌
해부학잡지
CHINESE JOURNAL OF ANATOMY
2009年
6期
758-761
,共4页
刘卉%林晋%魏建恩%郑琳%周瑞祥
劉卉%林晉%魏建恩%鄭琳%週瑞祥
류훼%림진%위건은%정림%주서상
松果体%褪黑素%胸腺%巨噬细胞%酪氨酸激酶受体B%大鼠
鬆果體%褪黑素%胸腺%巨噬細胞%酪氨痠激酶受體B%大鼠
송과체%퇴흑소%흉선%거서세포%락안산격매수체B%대서
pineal gland%melatonin%thymus%macrophage%tryrosin kinase receptor B%rat
目的:研究松果体摘除及补充褪黑素对大鼠胸腺巨噬细胞酪氨酸激酶受体B(trkB)表达的影响.方法:选用2月龄清洁级SD大鼠,分为正常对照组、假手术对照组、松果体摘除组、松果体摘除+褪黑素注射7.5mg·kg~(-1)·d~(-1)组和松果体摘除+褪黑素腹腔15mg·kg~(-1)·d~(-1)组,术后4、 8周取材.应用trkB和单克隆抗体ED1免疫荧光双标显色法观察分析松果体摘除及补充外源性褪黑素后胸腺巨噬细胞trkB表达的变化.结果:与对照组相比,松果体摘除术后4周胸腺双阳性细胞表达减弱,补充褪黑素后无变化.术后8周松果体摘除组与对照组相比无明显差异,而低剂量组双阳性细胞表达异常增高,高剂量组恢复正常.各组平均灰度无明显差异.结论:松果体及褪黑素在影响胸腺细胞分化发育过程中,胸腺巨噬细胞表达的trkB也随之发生变化,其与胸腺细胞表达的trkB共同作用参与胸腺细胞分化发育.胸腺神经内分泌微环境的分泌调节是松果体及褪黑素保护胸腺细胞的通路之一.
目的:研究鬆果體摘除及補充褪黑素對大鼠胸腺巨噬細胞酪氨痠激酶受體B(trkB)錶達的影響.方法:選用2月齡清潔級SD大鼠,分為正常對照組、假手術對照組、鬆果體摘除組、鬆果體摘除+褪黑素註射7.5mg·kg~(-1)·d~(-1)組和鬆果體摘除+褪黑素腹腔15mg·kg~(-1)·d~(-1)組,術後4、 8週取材.應用trkB和單剋隆抗體ED1免疫熒光雙標顯色法觀察分析鬆果體摘除及補充外源性褪黑素後胸腺巨噬細胞trkB錶達的變化.結果:與對照組相比,鬆果體摘除術後4週胸腺雙暘性細胞錶達減弱,補充褪黑素後無變化.術後8週鬆果體摘除組與對照組相比無明顯差異,而低劑量組雙暘性細胞錶達異常增高,高劑量組恢複正常.各組平均灰度無明顯差異.結論:鬆果體及褪黑素在影響胸腺細胞分化髮育過程中,胸腺巨噬細胞錶達的trkB也隨之髮生變化,其與胸腺細胞錶達的trkB共同作用參與胸腺細胞分化髮育.胸腺神經內分泌微環境的分泌調節是鬆果體及褪黑素保護胸腺細胞的通路之一.
목적:연구송과체적제급보충퇴흑소대대서흉선거서세포락안산격매수체B(trkB)표체적영향.방법:선용2월령청길급SD대서,분위정상대조조、가수술대조조、송과체적제조、송과체적제+퇴흑소주사7.5mg·kg~(-1)·d~(-1)조화송과체적제+퇴흑소복강15mg·kg~(-1)·d~(-1)조,술후4、 8주취재.응용trkB화단극륭항체ED1면역형광쌍표현색법관찰분석송과체적제급보충외원성퇴흑소후흉선거서세포trkB표체적변화.결과:여대조조상비,송과체적제술후4주흉선쌍양성세포표체감약,보충퇴흑소후무변화.술후8주송과체적제조여대조조상비무명현차이,이저제량조쌍양성세포표체이상증고,고제량조회복정상.각조평균회도무명현차이.결론:송과체급퇴흑소재영향흉선세포분화발육과정중,흉선거서세포표체적trkB야수지발생변화,기여흉선세포표체적trkB공동작용삼여흉선세포분화발육.흉선신경내분비미배경적분비조절시송과체급퇴흑소보호흉선세포적통로지일.
Objective: To study the effect of pinealectomy (Px) and melatonin (MLT) supplementation upon macrophages tryrosin kinase receptor B (trkB) expression in rat thymus. Methods: The clean 2-month-old rats were divided into five groups: normal control group, sham operation group, pinealectomized group, pinealectomy +7.5mg·kg~(-1)·d~(-1) MLT intraperitoneal injection group and pinealectomy +15mg·kg~(-1)·d~(-1) MLT intraperitoneal injection group, and their thymus were taken out at 4th week and 8th after operation. Double-immunofluorescent labeling for trkB and ectodermal dysplasia 1(ED1) antibody was used to observe and analyze the changes of double positive cells in thymus after Px and MLT supplementation. Results: Compared to the normal and sham group, the expression of thymic trkB~+ ED1~+ macrophages was weakened at 4th week after Px. MLT supplementation made no difference in the number of double positive cells and positive areas at the same time. But trkB~+ ED1~+ macrophage showed no significant change compared to the normal and sham group at the 8th week after Px, and the expression of macrophages increased significantly in the low dose group at the 8th week, and returned to normal in the high dose group at the 8th week. The average gray scale of double positive cells showed no significant difference among all groups. Conclusion: Macrophage trkB expression of thymic is also influenced by pineal gland and MLT, which participate in the differentiation and development of thymocytes with trkB expression. The adjustment of thymus neuroendocine microenvironment is one of the gateways in maintaining the thymocytes by pineal gland and MLT.