Abstract

Cell-cultivated fish offers the potential for a more ethical, sustainable, and safe seafood system. However, fish cell culture is relatively understudied in comparison to mammalian cells. Here, we established and characterized a continuous Atlantic mackerel (Scomber scombrus) skeletal muscle cell line (“Mack” cells). The cells were isolated from muscle biopsies of fresh-caught fish, with separate isolations performed from two distinct fish. Mack1 cells (cells from the first isolation) were cultured for over a year and subcultured over 130 times. The cells proliferated at initial doubling times of 63.9 h (± 19.1 SD). After a spontaneous immortalization crisis from passages 37–43, the cells proliferated at doubling times of 24.3 h (± 4.91 SD). A muscle phenotype was confirmed through characterization of muscle stemness and differentiation via paired-box protein 7 and myosin heavy chain immunostaining, respectively. An adipocyte-like phenotype was also demonstrated for the cells through lipid accumulation, confirmed via Oil Red O staining and quantification of neutral lipids. New qPCR primers (HPRT, PAX3B, MYOD1, MYOG, TNNT3A, and PPARG) were tailored to the mackerel genome and used to characterize mackerel cell genotypes. This work provides the first spontaneously immortalized fish muscle cell line for research, ideally serving as a reference for subsequent investigation.

Details

Title
Continuous fish muscle cell line with capacity for myogenic and adipogenic-like phenotypes
Author
Saad, Michael K. 1 ; Yuen, John S. K. 1 ; Joyce, Connor M. 1 ; Li, Xinxin 1 ; Lim, Taehwan 1 ; Wolfson, Talia L. 1 ; Wu, Justin 1 ; Laird, Jason 2 ; Vissapragada, Sanjana 1 ; Calkins, Olivia P. 1 ; Ali, Adham 1 ; Kaplan, David L. 1 

 Tufts University, Biomedical Engineering Department, Tissue Engineering Resource Center, Medford, USA (GRID:grid.429997.8) (ISNI:0000 0004 1936 7531) 
 Tufts University, Research Technology, Somerville, USA (GRID:grid.429997.8) (ISNI:0000 0004 1936 7531) 
Pages
5098
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2792254504
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.