熊本大学のノウハウを活かした新たなカタチの大学院教育

英語
日本
セミナー・シンポジウム及び募集
Seminar & Symposium/Admissions
2020-05-27

最先端研究セミナー

※ Zoom開催。URLMoodleの「HIGO最先端セミナー」にてご確認ください。

 

講演者: 依馬 正次(滋賀医科大学 動物生命科学研究センター 幹細胞・ヒト疾患モデル研究分野 教授)

演題: Human Disease Modeling with Genetically-Engineered Cynomolgus Monkeys

 

日時: 2020年527日(水)12:00-13:00

会場: Zoom開催。URLMoodleの「HIGO最先端セミナー」にてご確認ください。

 

Abstract:

Nonhuman primates (NHPs) are considered one of the most valuable animal models, because NHPs are closer to humans in organ size and anatomical structure, and therefore may have higher potential to recapitulate human diseases, while difficult genetic manipulation is a major obstacle for creation of human disease models. So far, we have established lentivirus-mediated techniques to generate transgenic (Tg) cynomolgus monkeys and created Tg monkeys overexpressing Amyloid beta Precursor Protein with the Alzheimer’s disease mutations. We also have established efficient genome editing technique in cynomolgus monkeys with CRISPR/Cas9, and explored an intractable human disease, Autosomal dominant polycystic kidney disease (ADPKD). We found that homozygous disruption of PKD1 allele, a causative gene for ADPKD can result in the massive renal cyst development, while PKD1 heterozygotes exhibited renal cysts during fetal stages, showing the recapitulation of some of features of human ADPKD pathology. I would like to talk about recent progress and future direction on development of genetically engineered NHPs and its application to human disease modeling.

 

References:

Seita Y et al., Sci Rep. 6:24868. (2016)

Seita Y et al., Biol Reprod. 100(6):1440-1452. (2019)

Seita Y et a., J Alzheimers Dis 75 (1): 45-60. (2020)

Kobayashi K et al., Stem Cell Res. 37:101439. (2019)

Tsukiyama T et al., Nat. Commun 10(1):5517. (2019)

 

担当分野: 腎臓発生分野 西中村(内線:6615

※ 詳細はこちらから