2022
DOI: 10.1016/j.foodres.2022.112206
|View full text |Cite
|
Sign up to set email alerts
|

An efficient and economical way to obtain porcine muscle stem cells for cultured meat production

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
9
0
1

Year Published

2023
2023
2024
2024

Publication Types

Select...
9

Relationship

1
8

Authors

Journals

citations
Cited by 20 publications
(16 citation statements)
references
References 45 publications
0
9
0
1
Order By: Relevance
“…PSCs were isolated from large white pigs as reported previously. 22 PSCs at passage 4 (P4) to P8 were seeded on flasks or plates pre-coated with 0.05% of fibrinogen (Sigma-Aldrich, Burlington, MA, USA) and cultured in PM.…”
Section: Methodsmentioning
confidence: 99%
“…PSCs were isolated from large white pigs as reported previously. 22 PSCs at passage 4 (P4) to P8 were seeded on flasks or plates pre-coated with 0.05% of fibrinogen (Sigma-Aldrich, Burlington, MA, USA) and cultured in PM.…”
Section: Methodsmentioning
confidence: 99%
“…Seed cells are crucial as they determine the quality and efficiency of cultured meat production. The number of high-quality seed cells was five times greater than low-quality seed cells after 20 days of expansion . Various types of cells have been reported for cultured meat production, with the most promising being muscle stem cells. , …”
Section: Introductionmentioning
confidence: 94%
“…The number of high-quality seed cells was five times greater than low-quality seed cells after 20 days of expansion. 4 Various types of cells have been reported for cultured meat production, with the most promising being muscle stem cells. 5,6 Muscle stem cells with high proliferation rates can multiply in large numbers, thus making it possible to cultivate meat products that resemble muscle fibers.…”
Section: Introductionmentioning
confidence: 99%
“…-When comparing the expansion and differentiation efficacy of cells separated using FACS and MuSCs, 0.5 h pre-plating cells were superior. Li, Wang [30] Chicken (embryos) -Cells were cultured on a collagen-coated flask for different times (2, 3, and 4 h). Subsequently, the non-adherent cells were transferred and cultured for 2 h at 37 -Cells were cultured on a collagen-coated dish for 16 h. -The non-adherent cells were transferred and cultured for 3 h. -The non-adherent cells were transferred and cultured for 24 h. -After 24 h, the media was replaced with fresh media and cultured for an additional 24 h. -The attached cells were detached and transferred to a collagen-coated dish.…”
Section: Redshaw Mcorist [25]mentioning
confidence: 99%