Quality Control of Stem Cell-Based Cultured Meat According to Specific Differentiation Abilities

Author:

Naraoka Yuna1ORCID,Mabuchi Yo12,Kiuchi Mai1,Kumagai Kyoko1,Hisamatsu Daisuke1ORCID,Yoneyama Yosuke3,Takebe Takanori345678,Akazawa Chihiro1

Affiliation:

1. Intractable Disease Research Center, Juntendo University Graduate School of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo 113-8421, Japan

2. Department of Clinical Regenerative Medicine, Fujita Medical Innovation Center, Fujita Health University, 1-1-4, Hanedakuko, Ota-ku, Tokyo 144-0041, Japan

3. Institute of Research, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan

4. Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children Hospital Medical Center, Cincinnati, OH 45229-3039, USA

5. Division of Developmental Biology, Cincinnati Children Hospital Medical Center, Cincinnati, OH 45229-3039, USA

6. Center for Stem Cell and Organoid Medicine (CuSTOM), Cincinnati Children Hospital Medical Center, Cincinnati, OH 45229-3039, USA

7. Premium Research Institute for Human Metaverse Medicine (WPI-PRIMe), Osaka University, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan

8. Department of Genome Biology, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan

Abstract

The demand for stem cell-based cultured meat as an alternative protein source is increasing in response to global food scarcity. However, the definition of quality controls, including appropriate growth factors and cell characteristics, remains incomplete. Cluster of differentiation (CD) 29 is ubiquitously expressed in bovine muscle tissue and is a marker of progenitor cells in cultured meat. However, CD29+ cells are naturally heterogeneous, and this quality control issue must be resolved. In this study, the aim was to identify the subpopulation of the CD29+ cell population with potential utility in cultured meat production. The CD29+ cell population exhibited heterogeneity, discernible through the CD44 and CD344 markers. CD29+CD44−CD344− cells displayed the ability for long-term culture, demonstrating high adipogenic potential and substantial lipid droplet accumulation, even within 3D cultures. Conversely, CD29+CD44+ cells exhibited rapid proliferation but were not viable for prolonged culture. Using cells suitable for adipocyte and muscle differentiation, we successfully designed meat buds, especially those rich in fat. Collectively, the identification and comprehension of distinct cell populations within bovine tissues contribute to quality control predictions in meat production. They also aid in establishing a stable and reliable cultured meat production technique.

Funder

JST-Mirai Program

Otsuka Holdings Co., Ltd.

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science, and Technology (MEXT) KAKENHI

Publisher

MDPI AG

Reference68 articles.

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3. Reassessment of adipocyte technology for cellular agriculture of alternative fat;Sugii;Compr. Rev. Food Sci. Food Saf.,2022

4. Stout, A.J., Mirliani, A.B., Rittenberg, M.L., Shub, M., White, E.C., Yuen, J.S.K., and Kaplan, D.L. (2022). Simple and effective serum-free medium for sustained expansion of bovine satellite cells for cell cultured meat. Commun. Biol., 5.

5. Microcarriers for Upscaling Cultured Meat Production;Bodiou;Front. Nutr.,2020

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