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不同培养方法对组织工程化小鼠角膜上皮构建影响的比较研究(英文) 被引量:4

Comparative study of four culture methods to engineer murine corneal epithelial sheet
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摘要 目的:探讨滋养细胞在小鼠角膜上皮细胞复层化中的作用,并研究构建组织工程化角膜上皮的理想方法。方法:在Transwell气液界面培养系统中,分别采用接触滋养层培养法、分离滋养层培养法、复式滋养层培养法以及无滋养层培养法等4种方法进行组织工程化小鼠角膜上皮的重建。HE染色进行组织学观察,免疫荧光法检测p63、角蛋白19以及involucrin的表达。结果:接触滋养层培养法、分离滋养层培养法中,角膜上皮复层化为3-4层;复式滋养层培养法中,角膜上皮复层化达5-7层;而无滋养层培养法中,复层化仅为2-3层。复式滋养层培养法构建的小鼠角膜上皮,基底细胞层和基底细胞上层表达祖细胞标记p63和角蛋白19,角膜上皮全层均表达分化标记involucrin。结论:复式滋养层培养法为构建组织工程化小鼠角膜上皮的理想方法。 AIM: To investigate the roles of feeder cells in stratification of murine corneal epithelial cells and build an ideal method to engineer stratified epithelial sheet. METHODS: Using contact feeder culture, separated feeder culture, compound feeder culture and culture without feeder cells by Air-lifting method in Transwell chamber culture system, tissue engineered corneal epithelium was reconstructed. Corneal sheets were stained with hematoxylin and eosin (HE) for histological observation. The expression of p63 and keratin 19 (K19) and involucrin (IVL) was investigated by immunocytochemistry analysis. RESULTS: Stratification was limited to three to four layers in the contact feeder group, whereas separate feeder sheets were slightly more stratified. The compound feeder group produced a stratified epithelium with five to seven layers of cells. The group without 3T3 feeder cells formed only two to three layers of cells. Immunostaining images in the compound feeder group showed expression of progenitor markers p63 and K19 in the basal and suprabasal layer, as well as differentiation marker involucrin in all layers. CONCLUSION: The remarkable stratification as well as the limbal phenotype makes the compound feeder system a candidate tool for cultivating transplantable epithelial sheets.
出处 《国际眼科杂志》 CAS 2008年第9期1743-1746,共4页 International Eye Science
基金 Liaoning Provincal Department of Education (No. 05L564)~~
关键词 小鼠 角膜 上皮 细胞培养 组织工程 mouse cornea epithelium cell culture tissue engineering
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参考文献17

  • 1Ang LP, Tan DT. Ocular surface stem cells and disease: current concepts and clinical applications. Ann Acad Med Singapore 2004 ; 33 (5) :576-580
  • 2Fernandes M, Sangwan VS, Rao SK, Basti S, Sridher MS, Bansal AK, Dua HS. Limbal stem cell transplantation.Indian J Ophthalmol 2004;52 (1):5-22
  • 3Hazlett L, Masinick S, Mezger B, Barrett R, Kurpakus M, Garrett M. Uhrastructural, immunohistological and biochemical characterization of cultured mouse corneal epithelial cells. Opbtbahnic research 1996; 28 ( 1 ) :50-56
  • 4Smola H, Thiekotter G, Fusenig NE. Mutual induction of growth factor gene expression by epidermal-dermal cell interaction. J Cell Biol 1993; 122(2) :417- 429
  • 5Szabowski A, Maas-Szabowski N, Andrecht S, Kolbus A, SchorppKistner M, Fusenig NE, Angel P. c-Jun and JunB antagonistically control cytokine-regulated mesenchymal-epidermal interaction in skin. Cell 2000 ; 103 ( 5 ) : 745-755
  • 6Rheinwald JG. Green H. Serial cultivation of strains of human epidermal keratinocytes : the formation of keratinizing colonies from single cells. Cell 1975 ;6 ( 3 ) :331-343
  • 7Barrandon Y, Green H. Cell size as a determinant of the clone-forming ability of human keratinocytes.Proc Natl Acad Sci U S A 1985 ;82 ( 16 ) : 5390-5394
  • 8Fu B, Quintero J, Baker CC. Keratinocyte growth conditions modulate telomerase expression, senescence, and immortalization by human papillomavims type 16 E6 and E7 oneogenes. Cancer Res 2003; 63(22):7815-7824
  • 9Masson-Gadais B, Fug re C, Paguet C, Leclerc S, Lefort NR, Germain L, Guerin SL. The feeder layer-mediated extended lifetime of cultured human skin keratinocytes is associated with altered levels of the transcription factors Sp1 and Sp3.J Cell Pbysiol 2006( 3 ) ;206:831-842
  • 10Gailit J, Clark RA. Wound repair in the context of extracellular matrix. Curr Opin Cell Biol 1994 ; ( 5 ) : 717-725

同被引文献16

  • 1T Ezashi,P Das,RM Roberts.Low O2 tensions and the prevention of differentiation of hES cells. Proceedings of the National Academy of Sciences of the United States of America . 2005
  • 2Ma X,Shimmura S,Miyashita H,Yoshida S,Kubota M,Kawakita T,Tsubota K.Long-term culture and growth kinetics of murine corneal epithelial cells expanded from single corneas. Investigative Ophthalmology . 2009
  • 3Chen Z,de Paiva C S,Luo L,et al.Characterization of putative stem cell phenotype in human limbal epithelia. Stem Cells . 2004
  • 4Yoshida S,Shimmura S,Kawakita T,Miyashita H,Den S,Shimazaki J,Tsubota K.Cytokeratin 15 can be used to identify the limbal phenotype in normal and diseased ocular surfaces. Investigative Ophthalmology . 2006
  • 5Hernandez Galindo EE,Theiss C,Steuhl KP,Meller D.Gap junctional communication in microinjected human limbal and peripheral corneal epithelial cells cultured on intact amniotic membrane. Experimental Eye Research . 2003
  • 6Cipolleschi,MG,Dello Sbarba,P,Olivotto,M.The role of hypoxia in the maintenance of hematopoietic stem cells. Blood . 1993
  • 7Ngo MA,Sinitsyna NN,Qin Q, et al.Oxygen-dependent differentiation of human keratinocytes. Journal of Investigative Dermatology . 2007
  • 8HazlettL,,Masinick S,Mezger B,BarrettR,Kurpakus M,GarrettM.Ultrastructural, immunohistological and biochemical characterization of cultured mouse corneal epithelial cells. Ophthalmic Research . 1996
  • 9Widmaier EP,Raff H,Strang KT.Vander’s human physiology:the mechanisms of body function. . 2006
  • 10Ursula Schl (?)tzer-Schrehardt,Friedrich E Kruse.Identification and characterization of limbal stem cells. Experimental Eye Research . 2005

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