中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2010年
5期
854-857
,共4页
吴淑燕%王响英%杨刚%李苏安%黄瑞
吳淑燕%王響英%楊剛%李囌安%黃瑞
오숙연%왕향영%양강%리소안%황서
树突状细胞%超微结构%自噬%凋亡%小鼠
樹突狀細胞%超微結構%自噬%凋亡%小鼠
수돌상세포%초미결구%자서%조망%소서
背景:树突状细胞可激发初始型T细胞,是目前所知机体功能最强的专职抗原递呈细胞,但对其超微结构的研究鲜见报道.目的:观察小鼠髓系树突状细胞不同发育阶段以及CD40配基化和肿瘤坏死因子α刺激后树突状细胞的超微结构特征.方法:无菌取小鼠骨髓前体细胞,采用粒细胞一巨噬细胞集落刺激因子和白细胞介素4联合方案体外诱导获得未成熟树突状细胞,负载早期凋亡的肿瘤细胞后采用小鼠CD40L转基因CHO细胞和肿瘤坏死因子α刺激48 h,按常规方法制备超薄切片,透射电镜观察树突状细胞的超微结构特征.结果与结论:前体细胞及未成熟树突状细胞内有清晰可见的吞饮泡,未成熟树突状细胞的胞质内可见"C"形和环形溶酶体;凋亡肿瘤细胞负载的树突状细胞可见凋亡小体被吞噬或包裹的现象,小鼠CD40L转基因CHO细胞和肿瘤坏死因子α均可促进树突状细胞成熟,但肿瘤坏死因子α作用后,部分树突状细胞有自噬和凋亡改变.结果提示,小鼠骨髓来源树突状细胞在不同分化发育阶段有其特殊的超微结构表现,肿瘤坏死因子α可介导树突状细胞发生自噬和凋亡.
揹景:樹突狀細胞可激髮初始型T細胞,是目前所知機體功能最彊的專職抗原遞呈細胞,但對其超微結構的研究鮮見報道.目的:觀察小鼠髓繫樹突狀細胞不同髮育階段以及CD40配基化和腫瘤壞死因子α刺激後樹突狀細胞的超微結構特徵.方法:無菌取小鼠骨髓前體細胞,採用粒細胞一巨噬細胞集落刺激因子和白細胞介素4聯閤方案體外誘導穫得未成熟樹突狀細胞,負載早期凋亡的腫瘤細胞後採用小鼠CD40L轉基因CHO細胞和腫瘤壞死因子α刺激48 h,按常規方法製備超薄切片,透射電鏡觀察樹突狀細胞的超微結構特徵.結果與結論:前體細胞及未成熟樹突狀細胞內有清晰可見的吞飲泡,未成熟樹突狀細胞的胞質內可見"C"形和環形溶酶體;凋亡腫瘤細胞負載的樹突狀細胞可見凋亡小體被吞噬或包裹的現象,小鼠CD40L轉基因CHO細胞和腫瘤壞死因子α均可促進樹突狀細胞成熟,但腫瘤壞死因子α作用後,部分樹突狀細胞有自噬和凋亡改變.結果提示,小鼠骨髓來源樹突狀細胞在不同分化髮育階段有其特殊的超微結構錶現,腫瘤壞死因子α可介導樹突狀細胞髮生自噬和凋亡.
배경:수돌상세포가격발초시형T세포,시목전소지궤체공능최강적전직항원체정세포,단대기초미결구적연구선견보도.목적:관찰소서수계수돌상세포불동발육계단이급CD40배기화화종류배사인자α자격후수돌상세포적초미결구특정.방법:무균취소서골수전체세포,채용립세포일거서세포집락자격인자화백세포개소4연합방안체외유도획득미성숙수돌상세포,부재조기조망적종류세포후채용소서CD40L전기인CHO세포화종류배사인자α자격48 h,안상규방법제비초박절편,투사전경관찰수돌상세포적초미결구특정.결과여결론:전체세포급미성숙수돌상세포내유청석가견적탄음포,미성숙수돌상세포적포질내가견"C"형화배형용매체;조망종류세포부재적수돌상세포가견조망소체피탄서혹포과적현상,소서CD40L전기인CHO세포화종류배사인자α균가촉진수돌상세포성숙,단종류배사인자α작용후,부분수돌상세포유자서화조망개변.결과제시,소서골수래원수돌상세포재불동분화발육계단유기특수적초미결구표현,종류배사인자α가개도수돌상세포발생자서화조망.
BACKGROUND: Denddtic cells (DCs) constitute the dominant population of antigen presenting cells (APCs) by possessing potent ability to initiate T cell immunity. The ultrastructure study of DCs is less reported. OBJECTIVE: To investigate the ultrastructure of DCs from mice bone marrow at different maturation stages, and the morphology of DCs between CD40 ligation and tumor necrosis factor-alpha (TNF-α) stimulation in vitro. METHODS: Mice myeloid DCs were generated from bone marrow in vitro using granulocyte-macrophage colony-stimulating factor (GM-CSF)and interleukin-4 (IL-4). Immature DCs were loaded with apoptotic tumor cells (AP-DC), and AP-DC was then stimulated with CD40L-CHO cells and TNF-α for 48 hours, respectively. DCs were routinely sectioned, and ultrastructure was observed under transmission electron microscope. RESULTS AND CONCLUSION: Immature DCs showed a few short and blunt cytoplasmic processes, there were specific morphology lysosomes that liked earphone in some cells; DCs engulfing the apoptotic bodies were observed; sub-cellular structures between CD40 ligation and TNF-α stimulated DCs were different, the former had typical morphology of mature DCs which exhibited many dendritic protrusions, however, some DCs displayed apoptosis and autophagy after TNF-α stimulation. In a conclusion, CD40 ligation plays an essential role in myeloid DCs differentiation and maturation, TNF-α can mediate apoptosis and autophaqy of DCs.