胞外作用 的英文怎麼說

中文拼音 [bāowàizuòyòng]
胞外作用 英文
extracellular effect
  • : Ⅰ名詞1 (胞衣) afterbirth2 (同一個國家或民族的人) fellow countryman; compatriot Ⅱ形容詞(同胞...
  • : Ⅰ名詞1 (外面) outside; external side 2 (外國) foreign country 3 (以外) besides; beyond; in ...
  • : Ⅰ動詞1 (使用) use; employ; apply 2 (多用於否定: 需要) need 3 (敬辭: 吃; 喝) eat; drink Ⅱ名...
  1. First, to construct a recombinant plasmid pegfp - c - fos with c - fos promoter and egfp, and then transfect it into human bladder transitional cell carcinoma biu - 87 cell ; second, based on the changes of the expression of gfp in the biu - 87 cell which induced by the aconitine and hab toxins, the concentration of the hab toxins could be detected

    目的:構建一個含c - fos啟動子和egfp報告基因的pegfp - c - fos重組質粒載體。體轉染膀胱癌biu - 87細后,利赤潮毒素后細表達綠色熒光蛋白的變化來檢測赤潮毒素,初步建立一種以細為基礎受體水平的赤潮毒素檢測方法。
  2. Dendritic cells are characterized by their ability to efficiently present antigen, and are uniquely equipped to stimulate naive t cell responses. immature dendritic cells acquire antigens from throughout the peripheral body, then migrate to t - lymphocyte - dependent areas of lymph nodes. thus, dendritic cells act as bridges, operating at the interface of innate and acquired immunity

    為機體免疫系統中功能最強的專職性抗原提呈細( antigen - presentingcells , apc ) ,樹突狀細( dendriticcells , dc )能高效地攝取、加工處理和提呈抗原,具有較強的遷移能力,並能顯著地激活初始型t細以啟動t細免疫應答反應,此, dc與b細以及nk細等也存在著相互,可見, dc在連接天然免疫和獲得性免疫之間起著非常重要的
  3. Effect of filamin - c on extracellular signal - regulated kinase phosphorylation mediated by 1a - adrenergic receptor in hek293 cell

    腎上腺素受體介導細信號調節激酶磷酸化的影響
  4. In aerial parts of the plant the outer wall of the epidermis is usually covered by a waxy cuticle that prevents desiccation, protects the underlying cells from mechanical damage, and increases protection against fungi, bacteria, etc

    植物地上部分的表皮的最層通常覆蓋一層蠟質角質層,起保護以防止過渡蒸騰,並使下方的細免於機械損傷,同時增加對真菌、細菌等的防禦能力。
  5. Not only the neurons but also the as in the rat brain play a very important role in the process of the peripheral nociceptive stimulation ; ? he newly - found eda may be the functional intercommunication ultrastructure between neurons and as, through which the as could modulate the neurons in the pain signal processing ; @ as might play an active and important role for modulation of pain through a new pathway from the peripheral afferent nerve to the as, then to neurons via electron - dense areas forming the glia - neuron s ignaling network

    光、電鏡水平發現as與神經元之間有多種途徑進行信息交流,新發現的eda有可能是神經元與as之間信息交流的結構之一。阻斷as與神經元間信息交流連接后,前者對周組織4第四軍醫大學博士學位論文損傷所致疼痛的反應不受影響,而後者的反應明顯受到抑制,提示在非病理性疼痛反應中,膠質細對神經元具有主動調控
  6. On the other hand, there is substanial evidences tha dcs mediate tolerane. the gm - csf - stbolated mouse bone mwderived mhc class ii + dc progendors tha are deficient in cell surface erpression of the costbolatory molecules b7 - l and b7 - 2 can induce alloanginspecific t ceil anergy in vbo. systendc adchstraion of these donor - derived dc progendors to recipients intravenously 7 days before transplantation prolonged the median graft survival tane from 9. 5 days to 22 days wbout additional twnosuppressions in a mouse cardinc twlanation model

    1995年, lul等報道表面缺乏共刺激分子,特別是缺乏cd80 ( b7 - 1 )和cd86 ( b7 - 2 )的未成熟型dc能在體誘導同種抗原特異性的t細無能,而對dc的適當處理能夠使未成熟型dc潛在的耐受原性得以放大和增強,使得dc在誘導免疫耐受中具有相當重要的及潛在的應價值。
  7. A purine - sensitive signaling pathway controls axon regeneration in goldfish retinal ganglion cells

    族維生素對體培養大鼠視網膜神經細及節細的神經營養
  8. Functions : it can resist oxidation and aging. enhance physical strength and capacity of brainwork. activate skin cells. intensify skin elaseicity, reduce wrinkes, and etc

    功效:具有抗氧化、抗衰老、提高體力和腦力勞動的能力。此,還具有活化皮膚細、增強皮膚彈性,減少皺紋等
  9. Effect of nf - b on human ciliary muscle cells in vitro

    對體培養的人睫狀肌細
  10. The influence of light adaptation on the ultrastructure of the photoreceptor in penaeus monodon fabriciu the form and the fine structure of compound eyes in penaeus monodon fabriciuwere studied by e lectron microscopy

    ,在無脊椎動物的光轉導過程中,經研究發現,鈣離子可能起著重要的, lisman和brown已經提出鈣離子是光適應時的內信使。
  11. The expression of viral antigens on the cell surface and disruption of the cytoskeleton can cause the cell - to - cell interactions and cellular appearance to change, making the cell a target for immune cytolysis

    病毒抗原在細表面表達,以及細骨架的破壞能引起細相互,細形會改變,導致細成為免疫殺傷的靶位。
  12. More recently, the laboratory has focused on natural killer cells and their roles in peripheral blood and in the pregnant uterine decidua

    最近,實驗室已經把目光投向了自然殺傷細以及它們在周血和懷孕時子宮蛻膜中的
  13. It is well known that various kinds of biological substances such as growth factors, cytokines and adhesion molecules are closely related with the wound healing process. in particular, adhesion molecules play an important role in the promotion of inflammatory reaction, these factors stimulate the synthesis of extracellular matrix by local fibroblasts, generate new blood vessels, promote the granulation tissue fonnation, and enhance re - epithelialization nthat takes places by the migration of the kerati - nocytes from the edges of the wound toward the center

    多種生物學介質如:生長因子、細因子及粘附分子等與皮膚損傷愈合過程密切相關,尤為值得提出的是,粘附分子在炎癥的發生的起始過程中起著至關重要的,這些因子在細基質的形成、血管的發生、肉芽組織的生成及上皮的再形成方面等均具有重要
  14. Abstract : this paper describes the role of the sialylsugar chains on cell surface in the attacking process of the influenza virus, and also binding specificity of hemagglutinin of the influenza virus to the sialylsugar chains

    文摘:介紹了細表面上含唾液酸的糖鏈在流感病毒侵襲細中的以及糖鏈與流感病毒表面糖蛋白-血凝素結合的特異性。
  15. Effects of ganoderma lucidum pllysaccharides on inositol trisphosphate ani diacylgiyceroi in murine t cells

    三磷酸肌醇和二酰基甘油體的研究
  16. Evidences showed that it contributed to proliferation and differentiation of many kinds of cells, and gm - csf also improved the livability of neuron in vitro and reduced its apoptosis rate

    研究表明gm - csf能明顯提高神經元的存活率,降低凋亡率,但其對神經幹細及機制,現尚不清楚。
  17. Effects of n, n - di - m - meth

    1細的研究
  18. In this report, we mainly covered the following aspects of " tissue organ regeneration and replication in situ " : 1 ) procedures of tissue organd regeneration and replication and replication in clnical practice ; 2 ) the discover and existence of potentiald regenerative cell ( prc ) ; 3 ) the proliferation, differentiation and regeneration law of potential law of potential regenerative cells ; 4 ) study procedure on tissue organ regeneration and replication from prcs in vitro based on the model of full skin organ regeneration in situ after extensive in vitro, set up the method and technology of searching life regenerative substance required in tissue organ regeneration and replication in situ. in this study, first, the whole human body is divided into 206 function units, which are the " tissue organ " in regeneration study. then the histology foundation of tissue organ regeneration and replication in situ is set up. in ordre to prove the existence of the potential regenerative cells and their potential baility and function, we established clinical tracking rechnique of skin organ regeneration in situ ; meanwhile, several tissue organ regeneration and replication in vitro models which represent different kinds of runctions were sucessfully set up, with all these techniques and models, we confirmed : 1 ) the existence, function and ability of pptemtoa regenerative cells ; 2 ) the importance of life regenerative substance ; 3 ) the feasibility of tissue organ regeneration and replication in situ ; 4 ) the big value of tissue organ regeneration and replication in situ in life science and medicine progerss. we also showed the possible foreground of capture cancer with this method and technologh. in this report, nearly 200 photographs of several tissue organ regeneration and replication in situ or in vitro demonstrated the whole process of tissue organ and big organ entities regeneration and replication from cells. the results of tissue organ regeneration and replication in situ mainly include : 1 ) whole skin organ regeneration and replication in situ ; 2 ) gastrointestinal mucosa tissue organ regeneration in vitro ; 3 ) hair follicle tissue organ regeneration in situ or in vitro ; 4 ) never tissue organ regeneration in situ ; 5 ) pancreas tissue organ regeneration and replication in vitro ; 5 ) marrow tissue regeneration in vitro ; 6 ) renal glomerulus and tubule tissue organ tugeneraation in vitro ; 7 ) heart muscle regeneration in vitro, etcl. in order to let more and more people know and understand this technology of tissue organd regeneration and replication in situ, herein, for the first time, we publicize the key points of actualizing this technology. also, we publicized the technology procedures and the frame constitute of life substances. we bilieve this is a big contribution to human science

    本研究報告,重點報道了組織器官的原位再生復制的臨床程序,報道了組織潛能再生細的發現和存在,以及該細的增殖分化和形成組織器官的變化規律.以燒傷后皮膚組織器官的原位再生復制為模型,研究出了體組織潛能再生細復制組織器官的培養方法;以體組織器官的復制為模型,建立了尋找原位組織器官再生復制所需生命物質的方法和技術.本研究,首先按人體的器官功能,分解為206個功能單位,確立了所復制的人體器官中的組織功能單位為組織器官,從而建立了原位組織器官再生復制的組織學基礎.為了驗證組織潛能再生細的再生潛能,建立了皮膚器官原位再生的實體臨床跟蹤技術,同時又建立了能代表有關器官功能類別的代表組織器官的原位和體復制模型,以多組織器官的成功復制確定潛能再生細,確定生命研究再生物質的重要性,確定組織器官原位再生復制的可行性,確定了組織器官原位再生復制的生命科學研究和醫學進步的重大應價值,同時展示了此方法和技術攻克癌癥的前景.本研究報告,以近二百幅多個組織器官原位和體再生復制的實體圖片,展示了潛能再生細復制的組織器官和大器官司實體;展示了細再生復制器官的全過程.真實的報告了組織器官原位再生復制的成果.所公布的主要成果為:皮膚器官的原位再生復制;胃腸黏膜組織器官的原位和體再生復制;毛囊組織器官的原位和體再生復制;神經組織器官的原位復制;胰腺組織器官的體復制;骨髓組織的體復制;腎小球小管組織器官的體復制;心肌的體復制等.為了讓更多的人學會和掌握組織器官原位再生復制技術,本報告首次公布實施技術的重要環節和技術流程;首次公布了生命再生物質的框架和組成.者自費研究成果對人類生命科學的一大貢獻
  19. In vitro experiment research of the anti - glioma activity of the glioma vaccine made from dendritic cell

    樹突狀細瘤苗抗腦膠質細實驗研究
  20. Here we managed to make cultured mice peritoneal macrophages be directly influenced by oligochitosan, and be stimulated by ifn - r before oligochitosan added, then measured the changes of gene transcription and translation level of both il - 1 and imf - a, respectively by methods of relatively quantitive rt - pcr and elisa. first, rt - pcr results showed that 18 hours was the most effective time and 40ug / ml was the most effective concentration of oligochitosan, then by the same method, confirm that 4hours is the most effective time and loou / ml is the most effective concentration of ifn - r stimulating. because ifn - r can enhance il - 1 and tnf - a gene expression of macrophages alone, so add ifn - r to microphages alone for 22 hours, then examined by rt - pcr, the results showed that il - 1 and tnf - a gene expression have no remarkable difference compared with the blank contrast group

    ,由於ifn y單獨也可促進兩種細因子基因表達,故在巨噬細中加入ifn y單獨22h ,再經阿一pcr檢測,發現加ifn y的實驗組細的幾一lp和tnf a基因轉錄水平與空白對照組相比較無顯著性差異,可見,殼寡糖和ifn v對巨噬細il lp和tnf一口基因轉錄水平的影響在時間上無一致性,在殼寡糖最適時間時,僅受ifn y刺激的巨噬細il lp和tnf q基因轉錄己下降至刺激前水平,因此可以認為, ifn y的加入僅起到對巨噬細預刺激使之處于敏感狀態的,有利於增強殼寡糖對巨噬細
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