真皮細胞組織 的英文怎麼說

中文拼音 [zhēnpíxìbāozǔzhī]
真皮細胞組織 英文
dermis cells tissue
  • 真 : Ⅰ形容詞（真實） true; genuine; real Ⅱ副詞1 （的確; 實在） really; truly; indeed 2 （清楚確實） cl...
  • 皮 : Ⅰ名詞1 （人或物體表面的一層組織） skin 2 （皮革） leather; hide 3 （毛皮） fur 4 （包在外面的一層...
  • 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
  • 真皮 : corium; cutis vera; derma; dermis; rete mucosum真皮炎 chorionitis
  • 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] [...
  1. Features : it contains morocco chamomile extract and many kinds of natural plant extract like coneflower. can strengthen the blood circulation in the blood vessel under the eyes socket, active the skin collateral channels completely, promote skin blood circulation, strengthen the metabolism of eyes organization cells, activate the cutis cells ' life function, thus get rid of the black orbit effectively

    特點：含摩洛哥野洋甘菊花部萃取精華，紫錐花等多種天然植物精華，可增強眼圈皮下血管中的血液循環，全面活躍皮膚經絡，促進肌膚血脈循環，增強眼組織細胞代謝，激活真皮細胞的原生機能，從而有效祛除黑眼圈。
  2. Mps is stored in connective tissue cells, fibers, and the ground sub - stance of corium and subcutis, where, over longer periods of time, it reaches concentrations which must be considered biologically active

    Mps （多磺酸粘多糖）儲存於結締組織細胞、纖維組織以及真皮和皮下組織基質，並在經過更長一段時間后在該處達到具有生物活性的濃度。
  3. Under eye cream : with derma - refine technology is formulated to accelerate cellular metabolism. puffiness, dark circles and crepiness are visibly reduced

    下眼霜：運用真皮組織修復科技，加速細胞新陳代謝。有效減少眼袋、黑眼圈和幼紋。
  4. The histopathological study revealed acanthosis, papillomatosis and large amounts of xanthoma cells in the papillary dermis

    組織病理學檢查顯示表皮肥厚伴隨乳頭樣增殖，及真皮層有大量黃色瘤細胞浸潤。
  5. 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。
  6. 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
  7. Histopathologically, the dermis showed loose storiform arrangement of collagen bundles in a myxoid matrix, with spindled or stellate - shaped fibroblast - like cells, moderately accentuated vasculature and an increased number of mast cells

    組織病理學在真皮可見似纖維母細胞之梭狀細胞及星狀細胞鬆散地散布在黏液樣之基質中，血管構造及肥大細胞之量亦有增加。
  8. Negative pressure : deep massage produced by negative pressure acts on parts of body, lifting epidermis, dermis and subcutaneous fat layer, and stretching all layer ' s connective fibers, effectively decomposing subcutaneous fat by regularly vibrating, increasing the content of collagen protein and elastic fibers, tightening skin, and fighting aging

    機械壓力：通過機械壓力在身體各個部位進行深層按摩，把表皮、真皮及皮下脂肪層向上提起，並升展不同皮層的結締纖維，通過來回有規律的震動，有效分解皮下脂肪，並增加真皮細胞的膠原蛋白與彈性纖維數量，重組肌膚，收緊皮膚組織，對抗衰老現象。
  9. 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胞的發現和存在，以及該細胞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，研究出了體外組織潛能再生細胞復制組織器官的培養方法;以體外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胞的再生潛能，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外復制模型，以多組織器官的成功復制確定潛能再生細胞的作用，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用價值，同時展示了用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外再生復制的實體圖片，展示了潛能再生細胞復制的組織器官和大器官司實體;展示了細胞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外再生復制;毛囊組織器官的原位和體外再生復制;神經組織器官的原位復制;胰腺組織器官的體外復制;骨髓組織的體外復制;腎小球小管組織器官的體外復制;心肌的體外復制等.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.作者自費研究成果對人類生命科學的一大貢獻
  10. Using the electric frequency permeameter can compliment the penetration and absorbance of the la zephire breast abundance essence liquid, and help the unique lz natural plant active factors to release their effects

    電頻滲透儀可促進美胸精華液的滲透和吸收，使獨有的lz天然植物活性因子向乳房脂肪細胞層層釋放，傳遞熱量，微電流加熱真皮層來促進膠原蛋白和彈性組織的生成
  11. In control group, simple split - thickness skin autografts were transplanted on the rat ' s full thicknss defect wounds of dorsolumbar. 2 weeks, 3 weeks, and 4 weeks after transplantation ordinary observation and histological observation were employed. in comparison with the control group, the composite transplantation skin had no remarkable contraction and have a fine exterior

    術后2周、 3周、 4周職材作大體形態學觀察，組織學檢查，結果發現與對照組相比，復合移植區痰痕增生較輕，斷層自體皮與無細胞真皮基質復合移植后外觀優于單純斷層自體皮移植。
  12. A dermal substitute with good cell compatibility and tissue compatibility can be degraded and absorbed gradually after transplantation, and then a newly formed dermal tissue is developed at the wounded site

    真皮支架必須具有良好的細胞相容性和組織相容性，在移植創面后應能被機體逐漸降解吸收，並適合受體真皮組織的重建。
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