1996 Fiscal Year Final Research Report Summary
Fundamental study on establishment and application of embryostem cell(ESC) in domestic animals.
| Project/Area Number |
06454122
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Basic veterinary science/Basic zootechnical science
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| Research Institution | TOHOKU UNIVERSITY |
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Principal Investigator |
UMEZU Motoaki TOHOKU UNIVERSITY,AGRICULTURE,ASSOCIATE PROFESSOR, 農学部, 助教授 (30005649)
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| Co-Investigator(Kenkyū-buntansha) |
MATSUMOTO Hiromichi TOHOKU UNIVERSITY,AGRICULTURE,ASSISTANT PROFESSOR, 農学部, 助手 (70241552)
SASADA Hiroshi TOHOKU UNIVERSITY,AGRICULTURE,ASSISTANT PROFESSOR, 農学部, 助手 (90158931)
HOTA Minoru TOHOKU UNIVERSITY,AGRICULTURE,ASSOCIATE PROFESSOR, 農学部, 助教授 (00005670)
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| Project Period (FY) |
1995 – 1996
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| Keywords | ESC / ICM / PGC / rat / goat / feeder / EGC / LIF |
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| Research Abstract |
Embryo stem cell (ESC) is the cell line originated from embryo and maintatined in undifferentiated state with pluripotency or totipotency. The cell is utilized in model of gene disease and therapy and establishment of cell lines is not fully successful in another animals except in mouse. In 1995-1996, establishment of ESC lines was tried from embryo originated cell in cow and goat as a domestic animal and in rat as an experimental animal.
In cow, oocytes harvested from ovaries of abattoir were subjected to in vitro maturation, fertilization and development to blastocysts and the inner cell mass (ICM) from blastocysts were tried to passage culture. The tertiary passage was possible when mouse embryo fibro-blast cell (MEF) or STO cell was used as feeder cell. Sampling of bovine ovaries was stopped because the slaughter house in Sendai-shi was closed for outsider caused of 0-157 affair.
In goat, morula, ICM and embryo just prior to hatching that were originated from in vivo fertilized ova were subjected to passage culture using MEF cell or STO cell as feeder cell and undifferentiated state was maintained in secondary culture using ICM.
In rat, in vivo sampled molula, ICM and primordial germ cell (PCM) of 9 dpc were subjected to passage culture and the effect of feeder cell was screened using MEF,rat embryo fibro-blast (REF), and S1^4-m220. Colony formation with undifferentiation was confirmed in ICM and PGC when REF or S1^4-m220 was used as feeder. PGC was passaged for fifth culture and further examination is suggested to need the cell line formation from PGC.
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Research Products
(23 results)
