Characterization of 3D Organotypic Culture of Mouse Adipose-Derived Stem Cells

Author:

Son Tae Gen1,Seo Yoojin2,Kim Won-Tae1,Kim Meesun1,Choi Seon Jeong1,Choi Si Ho1,Sung Byung-Jun1,Min Jae-Seok3,Han Eon Chul3,Kim Hyung-Sik2ORCID

Affiliation:

1. Research Center, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea

2. Department of Oral Biochemistry, Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan 50612, Republic of Korea

3. Department of Surgery, Dongnam Institute of Radiological and Medical Science, Busan 46033, Republic of Korea

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.

Funder

Ministry of Science, ICT, and Future Planning

Bio & Medical Technology Development Program of the National Research Foundation

Publisher

MDPI AG

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