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  1. NTU Theses and Dissertations Repository
  2. 生命科學院
  3. 動物學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/75502
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dc.contributor.author舒佩芸zh_TW
dc.date.accessioned2021-07-01T08:13:33Z-
dc.date.available2021-07-01T08:13:33Z-
dc.date.issued1984
dc.identifier.citation1. Harrison, R. G. (1907). Observations on the living developing nerve fiber. Proc. Soc. Exp. Biol. Med. 4, 140-143.
2. Auclair, W. (1961). Cultivation of monolayer cultures of frog renal cells. Nature (London) 192, 467-468.
3. Wolf, K. & Quimby, M. C. (1964). Amphibian cell culture: Permanent cell line from bullfrog (Rana catesbeiana). Science 144, 1578-1580.
4. Rafferty, K. A., Jr. (1969). Mass culture of amphibian cells: Methods and observations concerning stability of cell type.In “ Biology of Amphibian Tumors” (M. Mizell, ed.), pp. 52-81. Springer-Verlag, New York.
5. Freed, J. J., and Mezger-Freed, L. (1970). Stable haploid cultured cell lines from frog embryos. Proc. Nat. Acad. Sci. U.S. 65,337-344.
6. Rafferty, K. A.,Jr. (1976). The physiology of amphibian cells in culture. In “ Physiology of the amphibian” (B. Lofts, ed.), pp 101-162. Acandemic Press, New York.
7. Duryee, W. R. (1965). Factors influencing development of tumors in frogs. Ann. N.Y. Acad. Sci. 126,58-85.
8. Homer, H. A. & H. C. MaCgregor. (1983). C value and cell volume : their significance in the evolution and development if amphibians. J. Cell Sci. 63,135-146.
9. Freed, J.J., R. H. Hoess; F.A. Angelosanto & H. C. Massey Jr. (1979). Survival and DNA repair in UV irradiated haploid and diploid cultured frog Rana-pipiens cells. Mutat. Res. 62, 325-240.
10. Kondo, H. & H. Ide. (1983). Long-term cultivation of amphibian melanophores. Exp. Cell Res.149, 247-256.
11. Ide, H. (1978). Transformation of amphibian xanthophores into melanophores in clonal culture. J. Exp. Zool. 203, 287-294.
12. Przybelski, R.J. & K. S. Tweedell. (1978). Karyotype analysis of a frog pronephric tumor cell line. Exp. Cell Biol. 46, 287-297.
13. Roseristein, B. & B. M. Ohlsson-Wilhelm. (1979). Isolation of UV sensitive clones from a haploid frog cell line. Somatic. Cell Genet. 5, 117-128.
14. Freed, J. J. , L. Mezger-Freed and S. A. Schatz. (1969). Characteristics of cell lines from haploid and diploid anuran embryos. In “ Biology of amphibian tumors ” ( H. Mizell. ed. ). pp. 101-111. Springer-Verlag, New York.
15. Wong, W. Y. & K. S. Tweedell.(1974). Two viruses from the lucke tumor isolated in a frog pronephric cell line. Proc. Soc. Exp. Biol. 1ed. 145, 1201-1206.
16. Arhtur, E. & M. Balls. (1971). Amphibian cells in vitro. I. Growth of Xenopus cells in a soft agar mediun and in an agar surface. Exp. Cell Res. 64, 113-118.
17. Balls, M. & R. S. Worley. (1973). Amphibian cells in vitro. II. Effects of variations in medium osmolarity on a permanent cell line isolated from Xenopus. Exp. Cell Res. 76, 333-336.
18. 丁雲源,朱耀明.中國水產第339期,青蛙養殖.P.P. 6-10.
19. Paul, J. (1975). Cell and Tissue Culture (5th ed.) Churchill Livingstone Edinburgh London.
20. Sack, C. H., Jr. & C. Obie.(19H1). Human cell transformation by simian virus 40. Exp. Cell Res. 134, 425-432.
21. Goin, O. B., C. J. Coin and K. Bachmann. (1968). DNA and amphibian life history. Copeia. 3, 532-540.
22. Burns, E. R. (1971). Synchronous and asynchronous DNA synthesis in multinucleated ehrlich ascites tumor cells compared with multinucleated cells cultured from froglung. EXp. Cell Res. 66, 152-156.
23. Folkman, J. & A. Moscona. (1978). Role of veil shape in growth control. Nature. 273, 345-349.
24. O’Neill, C. H., P. N. Riddle and P. W. Jordan. (1979). The relation between surface area and anchorage dependence of growth in hamster and mouse fibroblasts. Cell. 16, 909-910.
25. Erickson, C. A. & J. P. Trinkaus. (1976). Microvilli and blebs as sources of reserve surface membrane during cell spreading. Exp. Cell Res. 99, 375-384.
26. Cershman, H. & J.J. Rosen (1978). Cell adhesion and cell surface topography in aggregates of 3T3 and 5V40-virus-transformed 3T3 cells. J. Cell Biol. 76, 639-651.
27. Porter, K. R., D. H. Prescott and J. J.. Frye (1973a). J. Cell Biol. 57, 815-
28. Elliott R. M. & D. C. Kelly (1980). Frog Virus 3 replication induction and intra cellular distribution of polypeptides in infected cells. J. Virol. 33, 28-51.
29. Elliott, R. M. , R. Bravo and D. C. Kelly. (1980). Frog Virus 3 replication analysis of structural and nonstructural polypeptides in infected BHK cells by acidic and basic 2 dimensional gel electrophoresis. J. Virol. 33, 18-27.
30. Drillien, R., D. Spehner and A. Kirn (1977). Cell killing by FV-3 evidence for cell killing by single viral particles or single viral subunits. Biochem. Biophys. Res. Commum. 79, 105-111.
31. Willis, D. B., R. Coorha and A. Cranoff. (1979). Macromolecular synthesis in cells infected by frog virus 3. Virology. 98, 328-335.
32. Elliott, R. H. , M. K. Arnold and D. C. Kelly. (1979). The replication of FV-3 in an amphibian cell line XTC-2 derived from Xenopus-laevis. J. Gen. Virol. 44, 89-98.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/75502-
dc.description.abstract本實驗之目的,乃是在培養虎皮蛙之細胞。並研究適合此種細胞生長之環境因數,諸如溫度、滲透壓、犢牛血清濃度等,並就已培養出之各器官細胞,做其外形之觀察與比較,以期建立虎皮蛙之永久細胞株。俾對此種蛙類之病毒診斷研究能有所幫助。
目前已建立虎皮蛙之心臟、腎臟、舌、肺臟、脾臟、肝臟細胞之初級培養,均可在短期(7?11天)內形成密集細胞層。而繼代培養之細胞如心臟細胞已培養至第20代,舌及肺臟細胞已培養至第7?8代,生長情形相當良好。其他腎、脾、肝臟細胞,在初級培養時,細胞生長及□離現象極活?,易形成密集細胞層,但繼代培養後,細胞生長情形不妙,原因不明。
依據所培養之6種不同器官之細胞,發現初級培養細胞多為上皮樣細胞,而繼代培養細胞以紡錘形細胞佔優勢。在掃描式電子顯微鏡下觀察,發現心臟、腎臟、脾臟細胞其表面微絨毛(microvilli)數目極少,有少數較大之泡沫狀突起(blebs)。
虎皮蛙心臟細胞最適宜生長溫度為24?31℃,滲透壓值為150?250mOsm/kg時生長良好。細胞隨培養液之血清濃度增高,生長速率亦隨之變快。在2%及5%犢牛血清之培養液內,則生長極?緩慢,細胞表面附著效應約為13-16%,顯示細胞未變性。
zh_TW
dc.description.provenanceMade available in DSpace on 2021-07-01T08:13:33Z (GMT). No. of bitstreams: 0
Previous issue date: 1984
en
dc.description.tableofcontents一、 摘要------------------------i
二、 謝辭------------------------iii
三、 目錄------------------------iv
四、 內容------------------------1
第一章 緒言------------------------1
第二章 材料與方法------------------------4
第一節 材料------------------------4
2.1-1 虎皮蛙
2.1-2 林格試液
2.1-3 組織洗滌液
2.1-4 胰蛋白?溶液
2.1-5 培養液
2.1-6 不同滲透壓培養液之製備
2.1-7 不同犢牛血清濃度培養液之製備
第二節 方法------------------------9
2.2-1 虎皮蛙細胞之初級培養
2.2-2 繼代培養
2.2-3 溫度對蛙心臟細胞生長速率之影響
2.2-4 滲透壓對蛙心臟細胞生長速率之影響
2.2-5 血清濃度對蛙心臟細胞生長速率之影響
2.2-6 蛙心臟細胞之表面附著效應
2.2-7 細胞大小的測量
2.2-8 掃描式電子顯微鏡之觀察
第三章 結果------------------------15
3-1 虎皮蛙心臟細胞之初級培養及繼代培養
3-2 虎皮蛙腎臟細胞之初級培養及繼代培養
3-3 虎皮蛙舌細胞之初級培養及繼代培養
3-4 虎皮蛙肺臟細胞之初級培養及繼代培養
3-5 虎皮蛙脾臟細胞之初級培養及繼代培養
3-6 虎皮蛙肝臟細胞之初級培養及繼代培養
3-7 溫度對虎皮蛙心臟細胞生長速率之影響
3-8 滲透壓對虎皮蛙心臟細胞生長速率之影響
3-9 血清濃度對虎皮蛙心臟細胞生長速率之影響
3-10 虎皮蛙心臟細胞之表面附著效應
3-11 細胞大小之測量
第四章 討論------------------------24
五、 圖表------------------------29
六、 參考文獻------------------------48
dc.language.isozh-TW
dc.title虎皮蛙細胞培養及其特性之研究zh_TW
dc.titleStudies on the Characteristics of Cell Culture Derived from Tissues of Frog Rana tigerinaen
dc.date.schoolyear72-2
dc.description.degree碩士
dc.relation.page51
dc.rights.note未授權
dc.contributor.author-dept生命科學院zh_TW
dc.contributor.author-dept動物學研究所zh_TW
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