Development of cryopreservation system for cells and tissue constructs in regenerative medicine and transplantation
| Project/Area Number |
15H03039
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Medical systems
|
|---|
| Research Institution | National Center for Child Health and Development |
|---|
Principal Investigator |
MIYAMOTO Yoshitaka 国立研究開発法人国立成育医療研究センター, 細胞医療研究部, 上級研究員 (20425705)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
池内 真志 東京大学, 大学院情報理工学系研究科, 講師 (90377820)
大和屋 健二 東京理科大学, 理工学部応用生物科学科, 助教 (80447309)
山下 紘正 日本大学, 総合科学研究所, 准教授 (00470005)
|
|---|
| Co-Investigator(Renkei-kenkyūsha) |
MIYADO Kenji 国立成育医療研究センター, 細胞医療研究部, 室長 (60324844)
YAGI Tohru 東京工業大学, 工学院, 准教授 (90291096)
TERAMOTO Naozumi 千葉工業大学, 工学部, 准教授 (80327163)
NOGUCHI Hirofumi 琉球大学, 医学系研究科, 教授 (50378733)
|
|---|
| Research Collaborator |
IKUTA Koji
MIURA Takumi
|
|---|
| Project Period (FY) |
2015-04-01 – 2018-03-31
|
| Project Status |
Completed (Fiscal Year 2017)
|
| Budget Amount *help |
¥17,030,000 (Direct Cost: ¥13,100,000、Indirect Cost: ¥3,930,000)
Fiscal Year 2017: ¥3,250,000 (Direct Cost: ¥2,500,000、Indirect Cost: ¥750,000)
Fiscal Year 2016: ¥6,500,000 (Direct Cost: ¥5,000,000、Indirect Cost: ¥1,500,000)
Fiscal Year 2015: ¥7,280,000 (Direct Cost: ¥5,600,000、Indirect Cost: ¥1,680,000)
|
|---|
| Keywords | 移植・再生医療 / 細胞・組織 / マイクロ・ナノデバイス / 組織構築物 / 凍結保存 / 凍結保護剤 / 機能評価 / システム / 再生医療 / 移植医療 |
|---|
| Outline of Final Research Achievements |
In this study, we developed a novel (1) DMSO-free cryopreservation solution, (2) culture device for cryopreservation, and (3) freezing system. (1) In order to safely freeze cells, it is necessary to solve the problems such as the cytotoxicity of DMSO, the antigenicity change of animal-derived materials and the possibility of contamination with pathogens. We found an optimal composition of cryopreservation solution without DMSO and serum for human cells. (2) 3D culture device TASCL was used to create a large amount of human tissue-derived stem cell constructs having a uniform size. In addition, we successfully determined a vitrified freezing condition based on the effective composition of the freezing solution. (3) In order to control cell freezing, we succeeded in developing a freezing system with a stirling engine and in optimizing freezing conditions. Consequently, a cryopreservation system of cell tissue construct for regeneration and transplantation medical care was established.
|
Report
(4 results)
Research Products
(32 results)
-
-
[Journal Article] Ubiquitin-activating enzyme E1 inhibitor PYR-41 retards sperm enlargement after fusion to the egg.2018
Author(s)
Yoshida K, Kang W, Nakamura A, Kawano N, Hanai M, Miyado M, Miyamoto Y, Iwai M, Hamatani T, Saito H, Miyado K and Umezawa A.
-
Journal Title
Reprod Toxicol.
Volume: 76
Pages: 71-77
DOI
Related Report
Peer Reviewed
-
[Journal Article] Birth weights and Down syndrome in neonates delivered after frozen-thawed embryo transfer: Six-year study (2007-2012) on the national assisted reproduction registry data in Japan2017
Author(s)
Yamatoya K, Saito K, Saito T, Kang W, Nakamura A, Miyado M, Kawano N, Miyamoto Y, Umezawa A, Miyado K, Saito H
-
Journal Title
Reproductive Medicine and Biology
Volume: 16
Issue: 2
Pages: 228-234
DOI
Related Report
Peer Reviewed / Open Access
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
