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Characterization of 3D Organotypic Culture of Mouse Adipose-Derived Stem Cells.
Son, Tae Gen; Seo, Yoojin; Kim, Won-Tae; Kim, Meesun; Choi, Seon Jeong; Choi, Si Ho; Sung, Byung-Jun; Min, Jae-Seok; Han, Eon Chul; Kim, Hyung-Sik.
Affiliation
  • Son TG; Research Center, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea.
  • Seo Y; Department of Oral Biochemistry, Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan 50612, Republic of Korea.
  • Kim WT; Research Center, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea.
  • Kim M; Research Center, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea.
  • Choi SJ; Research Center, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea.
  • Choi SH; Research Center, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea.
  • Sung BJ; Research Center, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea.
  • Min JS; Department of Surgery, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea.
  • Han EC; Department of Surgery, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea.
  • Kim HS; Department of Oral Biochemistry, Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan 50612, Republic of Korea.
Int J Mol Sci ; 25(7)2024 Apr 01.
Article in En | MEDLINE | ID: mdl-38612741
ABSTRACT
Although stem cells are a promising avenue for harnessing the potential of adipose tissue, conventional two-dimensional (2D) culture methods have limitations. This study explored the use of three-dimensional (3D) cultures to preserve the regenerative potential of adipose-derived stem cells (ADSCs) and investigated their cellular properties. Flow cytometric analysis revealed significant variations in surface marker expressions between the two culture conditions. While 2D cultures showed robust surface marker expressions, 3D cultures exhibited reduced levels of CD44, CD90.2, and CD105. Adipogenic differentiation in 3D organotypic ADSCs faced challenges, with decreased organoid size and limited activation of adipogenesis-related genes. Key adipocyte markers, such as lipoprotein lipase (LPL) and adipoQ, were undetectable in 3D-cultured ADSCs, unlike positive controls in 2D-cultured mesenchymal stem cells (MSCs). Surprisingly, 3D-cultured ADSCs underwent mesenchymal-epithelial transition (MET), evidenced by increased E-cadherin and EpCAM expression and decreased mesenchymal markers. This study highlights successful ADSC organoid formation, notable MSC phenotype changes in 3D culture, adipogenic differentiation challenges, and a distinctive shift toward an epithelial-like state. These findings offer insights into the potential applications of 3D-cultured ADSCs in regenerative medicine, emphasizing the need for further exploration of underlying molecular mechanisms.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adiposity / Microphysiological Systems Limits: Animals Language: En Journal: Int J Mol Sci Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adiposity / Microphysiological Systems Limits: Animals Language: En Journal: Int J Mol Sci Year: 2024 Type: Article