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Development of Collagen-Based 3D Matrix for Gastrointestinal Tract-Derived Organoid Culture.
Jee, Joo Hyun; Lee, Dong Hyeon; Ko, Jisu; Hahn, Soojung; Jeong, Sang Yun; Kim, Han Kyung; Park, Enoch; Choi, Seon Young; Jeong, Sukin; Lee, Joong Woon; Cho, Han-Jun; Kwon, Min-Soo; Yoo, Jongman.
Afiliação
  • Jee JH; Department of Microbiology, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Lee DH; CHA Organoid Research Center, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Ko J; CHA Organoid Research Center, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Hahn S; Department of Physiology, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Jeong SY; Department of Microbiology, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Kim HK; CHA Organoid Research Center, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Park E; Department of Microbiology, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Choi SY; CHA Organoid Research Center, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Jeong S; Department of Microbiology, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Lee JW; CHA Organoid Research Center, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Cho HJ; Department of Microbiology, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Kwon MS; CHA Organoid Research Center, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
  • Yoo J; Department of Microbiology, School of Medicine, CHA University, Seongnam-si, Gyeonggi-do 13488, Republic of Korea.
Stem Cells Int ; 2019: 8472712, 2019.
Article em En | MEDLINE | ID: mdl-31312220
ABSTRACT
Organoid is a cell organization grown in a three-dimensional (3D) culture system which represents all characteristics of its origin. However, this organ-like structure requires supporting matrix to maintain its characteristics and functions. Matrigel, derived from mouse sarcoma, has often been used as the supporting matrix for organoids, but the result may not be desirable for clinical applications because of the unidentified components from the mouse sarcoma. On the other hand, natural characteristics of collagen emphasize toxic-free friendly niche to both organoid and normal tissue. Hence, this study attempts to develop a new, collagen-based matrix that may substitute Matrigel in organoid culture. Collagen-based matrix was made, using type 1 collagen, Ham's F12 nutrient mixture, and bicarbonate. Then, characteristics of mouse colon organoids were analyzed by morphology and quantitative messenger RNA (mRNA) expression, revealing that the mouse colon organoids grown in the collagen-based matrix and in Matrigel had quite similar morphology, specific markers, and proliferative rates. Mouse small intestine-derived organoids, stomach-derived organoids, and human colon-derived organoids were also cultured, all of which were successfully grown in the collagen-based matrix and had similar properties compared to those cultured in Matrigel. Furthermore, possibility of organoid transplantation was observed. When mouse colon organoids were transplanted with collagen matrix into the EDTA-colitis mouse model, colon organoids were successfully engrafted in damaged tissue. For that reason, the use of collagen-based matrix in organoid culture will render organoid cultivation less expensive and clinically applicable.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Stem Cells Int Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Stem Cells Int Ano de publicação: 2019 Tipo de documento: Article
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