Coculture of preimplantation embryo with an immortalized human oviductal epithelial cells
| Project/Area Number |
06671654
|
|---|
| Research Category |
Grant-in-Aid for General Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
Obstetrics and gynecology
|
|---|
| Research Institution | Tottori University, Faculty of Medicine |
|---|
Principal Investigator |
HARADA Tasuku Tottori Univ.・Dept.Obstet.Gynecol., Assistant Professor, 医学部・附属病院, 講師 (40218649)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
ONOHARA Yoshimasa Tottori Univ.・Dept.Obstet.Gynecol., Assistant Professor, 医学部, 助手 (00240862)
TANIKAWA Masahiro Tottori Univ.・Dept.Obstet.Gynecol., Assistant Professor, 医学部・附属病院, 助手 (90236688)
TERAKAWA Naoki Tottori Univ.・Dept.Obstet.Gynecol., Professor, 医学部, 教授 (90163906)
戸田 稔子 鳥取大学, 医学部, 助手 (10163990)
|
|---|
| Project Period (FY) |
1994 – 1995
|
| Project Status |
Completed (Fiscal Year 1995)
|
| Budget Amount *help |
¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 1995: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1994: ¥1,300,000 (Direct Cost: ¥1,300,000)
|
|---|
| Keywords | Oviductal epithelial cells / immortalize / basis fibroblast growth factor / FGF receptor 1 / 6FGF |
|---|
| Research Abstract |
We have tried establish an immortalized cell line of human tubal epithelium. It is not possible to obtain immortalized cells after repeated experiments. We also have performed experiments using preimplantation embryos. We determined the expression of fibroblast growth factor (FGF) -2 and the FGF receptor 1 (FGFR-1) mRNA in the mouse embryos and in epithelial cells of the uterine endometrium using reverse transcription-polymerase chain reaction (RT-PCR). No FGF-2 mRNA was detected in mouse embryos but FGFR-1 mRNA was expressed at the blastocyst stage. These results suggest importance of FGFR-1 in preimplantation development of embryo. To examine the mechanism of FGFR-1 expression, the arrangement of exons and introns encoding 5'-side of murine FGFR-1 gene was mapped. A large intron with a size of 14kb was identified between exon 1 and 2. All subtypes of FGFR-1 was obserbed to be generated through alternative aplicing. Furthermore, we characterized a transcription element of this gene. The basal promoter element was mapped to the 5'-flanking region from -89 to -43. The DNase I protection assay and gel shift analysis revealed that a nuclear protein could bind to the nucleotide sequence from -62 to -42. In conclusion, FGF-2 produced by the female reproductive tract may exert paracrine effects on preimplantation embryos. FGFR-1 gene has an unique genomic structure. The 5'-flanking region from -62 to -42 plays a pivotal role in FGFR-1 gene expression.
|
Report
(3 results)
Research Products
(6 results)
