In vitro characterization of proliferation and differentiation of pig satellite cells

• DOI: 10.1016/j.diff.2012.08.001
• Publication Date: 2012-09-27T09:37:06Z
• Authors: Marie-Hélène Perr...; Patrick Ecolan; Inge Lise Sorensen; Niels Oksbjerg; Louis Lefaucheur
• Keywords: pig; 0303 health sciences; Myosin Heavy Chains; Satellite Cells, Skeletal Muscle; [SDV]Life Sciences [q-bio]; Muscle Fibers, Skeletal; Sus scrofa; Cell Differentiation; fiber type; [SDV] Life Sciences [q-bio]; 03 medical and health sciences; Animals; satellite cell culture; Female; Cells, Cultured; Cell Proliferation

Skeletal muscle contains various muscle fiber types exhibiting different contractile properties based on the myosin heavy chain (MyHC) isoform profile. Muscle fiber type composition is highly variable and influences growth performance and meat quality, but underlying mechanisms regulating fiber type composition remain poorly understood. The aim of the present work was to develop a model based on muscle satellite cell culture to further investigate the regulation of adult MyHC isoforms expression in pig skeletal muscle. Satellite cells were harvested from the mostly fast-twitch glycolytic longissimus (LM) and predominantly slow-twitch oxidative rhomboideus (RM) muscles of 6-week-old piglets. Satellite cells were allowed to proliferate up to 80% confluence, reached after 7 day of proliferation (D7), and then induced to differentiate. Kinetics of proliferation and differentiation were similar between muscles and more than 95% of the cells were myogenic (desmin positive) at D7 with a fusion index reaching 65 ± 9% after 4 day of differentiation. One-dimensional SDS polyacrylamide gel electrophoresis revealed that satellite cells from both muscles only expressed the embryonic and fetal MyHC isoforms in culture, without any of the adult MyHC isoforms that were expressed in vivo. Interestingly, triiodothyronine (T3) induced de novo expression of adult fast and α-cardiac MyHC in vitro making our culture system a valuable tool to study de novo expression of adult MyHC isoforms and its regulation by intrinsic and/or extrinsic factors.