纖維細胞組織 的英文怎麼說
中文拼音 [xiānwéixìbāozǔzhī]
纖維細胞組織
英文
cellular tissue parenchyma- 纖 : 纖形容詞(細小) fine; minute
- 維 : Ⅰ動詞1 (連接) tie up; hold together; link 2 (保持; 保全) maintain; safeguard; preserve; keep ...
- 細 : 形容詞1 (條狀物橫剖面小) thin; slender 2 (顆粒小) in small particles; fine 3 (音量小) thin ...
- 胞 : 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...
- 組 : Ⅰ名詞1 (由不多的人員組成的單位) group 2 (姓氏) a surname Ⅱ動詞(組織) organize; form Ⅲ量詞(...
- 織 : 動詞(編織) knit; weave
- 纖維 : fibre; staple; filamentary
- 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
- 組織 : 1 (組織系統) organization; organized system 2 (組成) organize; form 3 [紡織] weave 4 [醫學] [...
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Typical pathological changes is leprosy granulation swollen namely leprosy is nodal, by composition of place of afterbirth of large and small of connective tissue of embedded leprosy bacili, there is epithelial appearance cell, oar cell to reach fiber cell all round
典型病變是麻風肉芽腫即麻風結節,由內含麻風桿菌結締組織巨細胞所組成,四周有上皮樣細胞、漿細胞及成纖維細胞。The image was obtained by taking multiple exposures through bandpass optical filter sets appropriate for fluorescein, texas red dye and dapi using a 100x plan apochromat objective
成纖維細胞分化為成軟骨細胞、成膠原細胞和成骨細胞,形成體內的纖維組織、肌腱、腱膜、各種支持組織和粘合組織。From dead chickens, one virrus was isolated by using eggs and chicken embryo fibroblast. lt was able to agglutinate chicken ' s erythrocytes and this heamagglutination could be inhibited by newcastle disease antiserum. this strain ' s biological property was tested by barren spot, cross - enutralization and cross - heamagglution inhibited and it was found that it was homological with the standard newcastle disease virus ( ndv ) virulent strain and avirulent strain but it had some diference with the standard strain
本實驗採用spf雞胚及雞胚原代成纖維細胞,從河北省某雞場新城疫免疫抗體很高的病死雞的腦組織中分離得到一株病毒。此株病毒能凝集雞的紅細胞,並且這種凝集可以被特異性抗血清所抑制。Cellular tissue parenchyma
纖維細胞組織In adults, fibroblasts in connective tissue rarely undergo division.
成年人結締組織的成纖維細胞很少發生分裂。The rse was then grafted to the dorsum of scid mice to evaluate its biocompatibility by histologic and immunohistochemistry analysis
將人包皮的表皮細胞和真皮的成纖維細胞復合到上述材料上培養7天後,移植到裸鼠背部,進行生物相容性、組織學和免疫組織化學的分析。Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel
結果如下:皮下包埋卜周者,無細胞真皮基質漸與周圍組織粘附,顏色由蒼白轉紅;皮下包埋3周者,無細胞真皮基質與周圍組織緊密枯附,盾晰葉辯;術后卜周,包埋的基質面積變化較包埋前無統計學差異o川0引,術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ) 。光鏡下術后卜周,宿主的淋巳組織細胞、成纖維細胞浸入生長,釉附在膠原纖維上,少量血管內皮細胞浸入基質;術后34周,無細胞真皮基質內較多的血管形成,故可認為無細胞真皮基質免疫原性低,能誘導宿主的成纖維細胞、巨噬細胞浸入生長,為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究, sd大鼠10隻,在其背部卜方造成全厚皮膚缺損的創面There are many adaptive changes in the two research subjects ( artemisia. songarica schrenk. and seriphidium. santolinum ( schrenk ) polijak. ) in morphology and anatomy, such as with the increase of the daily age, the root - shoots ratio increased ; the root became stronger ; the ratio of leaf volume and leaf area increased ; the volume of epidermic cell decreased ; the cut - icle and phellem layer on the surface of root thickened. stoma caved in leaf ; epidermal hair of leaf and stem well - developed, palisde tissue developed well, the cell gap decreased ; the spongy tissue disappeared ; leaf is kinds of isolateralthat is the typical xeromorphic structure ; crystal cell and fibric cell increased ; conducting tissue and mechanical tissue developed well ; bundle sheath appeared
實驗研究的兩種菊科( compositae )植物(準噶爾沙蒿( artemisiasongaricaschrenk )和沙漠絹蒿( seriphidiumsantolinum ( schrenk ) poljak . ) ) ,形態解剖方面的變化表現為:隨日齡增加,根長/株高比值日益增大;根系逐漸發達;體積與葉面積比逐漸增大;表皮細胞體積變小;角質層增厚;根外部出現加厚的木栓層;氣孔下陷;葉、莖部的表皮毛密布,柵欄組織日益發達;而細胞間隙日漸變小;海綿組織逐漸消失;葉面結構常為典型旱生結構? ?等葉面;晶細胞及纖維細胞數目增多;輸導組織、機械組織日漸發達;具有維管束鞘等等。When lying between connective tissue fibers, fibroblasts are generally elongated and spindle shaped.
當它位於結締組織纖維間時,纖維細胞一般呈長形及梭形。Part 1 : the culture and identification of es - d3 cells and the study of the efficiency of eb formation from es cells when grown on mef feeder layer in es culture medium or cultured in es culture medium supplemented with lif 1000u / ml, es - d3 cells being used in our experiments formed normal clones, expressed akp and kept their normal karyotype over many passages. the in vitro and in vivo differentiation experiments showed that es - d3 cells could differentiate into variety of cell types derived from three primary germ layers
結果顯示: eso3細胞在小鼠胚胎成纖維細胞上和或含白血病抑制因於億f )的es細胞培養液中形成典型的胚胎幹細胞克隆,堿性磷酸酶染色結果為強陽性,具有正常二倍體核型以及具有在體內外分化為三個胚層來源的組織細胞的潛能,而且具有形成種系嵌合動物的能力。At high magnification, granulation tissue has capillaries, fibroblasts, and a variable amount of inflammatory cells ( mostly mononuclear, but with the possibility of some pmn ' s being present )
高倍速鏡:肉芽組織由毛細血管、成纖維細胞和大量的各種炎細胞組成。炎細胞主要是單核細胞,也可以伴有嗜中性粒細胞的出現。In one word, the methods for producing acellulace matrix have not been standardized. in this study, we want to select the best way to produce acellular matrix. we also use immunohistochemical method for detecting the magor heterogenetic antigen a - galactosyl residues ( a - gal ) in acellular matrix
並應用免疫組化的方法檢測脫細胞后基質的主要異種抗原,用種植實驗觀察異種機體對脫細胞生物基質的組織反應倩況,另在其上種植鼠成纖維細胞以觀察脫細胞生物基質的細胞毒性和細胞相容問題。Differences of focal adhesion kinase signaling events between keloid and peri - keloid normal skin fibroblasts
瘢痕疙瘩組織及其周邊正常皮膚成纖維細胞斑點粘合激酶表達差異的意義( 3 ) isolation and culture of human primordial germ cells ( pgcs ). human pgcs collected from gonadal ridges and mesenteries were grown on mouse feeder layers in the presence of human recombinant leukemia inhibitory factor ( lif ), human recombinant basic fibroblast growth factor, and forskolin as described previously. initially, pgcs were visualized by alkaline phosphatase activity staining
( 3 )人類pgcs的分離和培養從4 10周齡藥物流產胚胎的生殖嵴和腸系膜組織中分離原始生殖細胞( primordialgermcells , pgcs ) ,培養在添加人重組白血病抑制因子( lif ) 、人重組堿性成纖維細胞生長因子( bfgf )和forskolin的小鼠飼養層細胞上。At the same time, growth factors have relation to genesis of tumor. fibroblast growth factor ( fgf ) can promote proliferation of tissues derived from mesoderm or neuroectoderm and many tissues and cells can secrete fgf
成纖維細胞生長因子( fgf )能夠誘導中胚層和神經外胚層來源細胞的增殖和分化,許多組織和細胞都可以分泌fgf , fgf可以促進多種細胞的生長和分化。The quality of feeder layer is affected by a lot of factors, such as animal breed, culture medium, passages in vitro and experiment condition, etc. as to the production of feeder layer, there are a few reports about morphological and histologic change when of embryonic body fibroblast when culturing in vitro and cryopreservation, so kunming mouse were chosen as experimental animals and morphological and histologic changes were studied in course of its embryonic body culturing. we expect to offer theoretical foundation to our laboratory for setting up feeder layer storehouse. at the same time, the feasibility of myocardium tissue culturing with fibroblast layer altogether was studied so that established foundation for studied the biological characteristic of heart outside body
小鼠胚體成纖維細胞的培養是制備飼養層的重要途徑,其制備、傳代及冷凍保存均有不同的研究報道,飼養層的質量受許多因素的影響,如動物的品種、培養液、所傳代數及實驗條件等,關于飼養層制備過程中的胚體細胞培養、傳代、冷凍后的細胞形態、組織學等方面的研究報道很少,故本實驗以昆明小白鼠為實驗動物,研究其胚體培養過程中細胞的形態學、組織學等方面的變化,以期為本實驗室建立飼養層細胞庫提供理論依據,同時探討心肌細胞和成纖維細胞層共培養的可行性,以期為心臟生物學特性的體外研究奠定基礎。Micronodular cirrhosis is seen along with moderate fatty change. note the regenerative nodule surrounded by fibrous connective tissue extending between portal regions
伴中度脂肪變性的小結節型肝硬化。注意再生的肝細胞小結節被匯管區之間的纖維結締組織包圍。In this study, the expression of nfkb p65 and ikba ( inhibitory kappa b alpha, ikba ) in poly - morphonnucleared cells, mononuclear cells and fibroblastic cells during rat skin contusion repair will be investigated using immunohistochemical technique and the relationship with contusion will be revealed, which can provide the theorical evidence to identify the contusion age
I b因其抑制nf b活性,也越來越受到人們的重視,故本實驗應用免疫組織化學方法觀察nf b家族的重要成員nf bp65與其抑制因子i b在大鼠皮膚挫傷后不同時間在多核粒細胞、單核巨噬細胞及成纖維細胞中的表達變化,揭示其與皮膚挫傷時間的關系,為皮膚挫傷時間的判定提供新的理論依據。Microscopically with cirrhosis, the regenerative nodules of hepatocytes are surrounded by fibrous connective tissue that bridges between portal tracts
用顯微鏡觀察肝硬化,肝細胞再生結節被橋接匯管區的纖維結締組織包繞。A type of plant tissue consisting of elongated cells with tapering ends, occurring in supporting and conducting tissue
纖維細胞組織一種植物組織,由有逐漸變細的尾的拉長的細胞構成,存在於支撐和引導組織中分享友人