Insulin stimulates myogenesis in a rat myoblast line
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After 7-9 days of culture, L6 myoblasts had fused into multinucleated myotubes.
“After 7–9 days of culture the myoblasts had fused into multinucleated myotubes 41.”
From Akt-dependent anabolic activity of natural and synthetic brassinosteroids in rat skeletal muscle cells (2011) · cites this paper as [41]
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PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 315,771 · see citing works
Retention of differentiation potentialities during prolonged cultivation of myogenic cells.
Yaffe, D. (1968) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.61.2.477 · Cited by 984 · see citing works
Biochemical actions of hormones
(1987) · General and Comparative Endocrinology · doi:10.1016/0016-6480(87)90137-7 · Cited by 576 · see citing works
Hershko, A., Mamont, P. S., Shields, R. L., & Tomkins, G. M. (1971) · Nature New Biology · doi:10.1038/newbio232206a0 · Cited by 516 · see citing works
Alterations of enzymatic activities during muscle differentiation in vitro
Shainberg, A., Yagil, G., & Yaffe, D. (1971) · Developmental Biology · doi:10.1016/0012-1606(71)90017-0 · Cited by 415 · see citing works
Modulation of Adenylate Cyclase Activity in Liver and Fat Cell Membranes by Insulin
Illiano, G., & Cuatrecasas, P. (1972) · Science · doi:10.1126/science.175.4024.906 · Cited by 243 · see citing works
Guanosine 3′:5′-Cyclic Monophosphate and the Action of Insulin and Acetylcholine
Illiano, G., Tell, G. P. E., Siegel, M. I., & Cuatrecasas, P. (1973) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.70.8.2443 · Cited by 229 · see citing works
Biochemical Actions of Hormones
(1980) · Elsevier eBooks · doi:10.1016/b978-0-12-452807-9.x5001-3 · Cited by 206 · see citing works
Piatigorsky, J. (1973) · Developmental Biology · doi:10.1016/0012-1606(73)90060-2 · Cited by 80 · see citing works
An Early Effect of Prolactin on the Formation of α-Lactalbumin by Mouse Mammary Epithelial Cells
Vonderhaar, B. K., Owens, I. S., & Topper, Y. J. (1973) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)44397-4 · Cited by 68 · see citing works
Wahrmann, J. P., WIN, R., & Luzzati, D. (1973) · Nature New Biology · doi:10.1038/newbio245112a0 · Cited by 66 · see citing works
HORMONAL REQUIREMENTS FOR MYOGENESIS OF STRIATED MUSCLE IN VITRO: INSULIN AND SOMATOTROPIN
Haba, G. D. L., Cooper, G., & Elting, V. (1966) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.56.6.1719 · Cited by 63 · see citing works
Zalin, R. J. (1973) · Experimental Cell Research · doi:10.1016/0014-4827(73)90049-9 · Cited by 43 · see citing works
Woo, Y., & Manery, J. F. (1973) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(73)90003-9 · Cited by 41 · see citing works
Haba, G. D. L., Cooper, G., & Elting, V. (1968) · Journal of Cellular Physiology · doi:10.1002/jcp.1040720105 · Cited by 36 · see citing works
An ATP pool with rapid turnover within the cell membrane
Reporter, M. (1972) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(72)90390-7 · Cited by 28 · see citing works
Wahrmann, J. P., Luzzati, D., & WINAND, R. J. (1973) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(73)90751-1 · Cited by 22 · see citing works
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A Myogenic Cell Line with Altered Serum Requirements for Differentiation
Yaffe, D., & Saxel, O. (1977) · Differentiation · doi:10.1111/j.1432-0436.1977.tb01507.x · Cited by 314 · see citing works
Hormonal control of muscle growth
Florini, J. R. (1987) · Muscle & Nerve · doi:10.1002/mus.880100702 · Cited by 313 · see citing works
Florini, J. R., Ewton, D. Z., & Roof, S. L. (1991) · Molecular Endocrinology · doi:10.1210/mend-5-5-718 · Cited by 257 · see citing works
Effects of growth factors on myogenic differentiation
Florini, J. R., & Magri, K. A. (1989) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1989.256.4.c701 · Cited by 205 · see citing works
Effect of fibroblast growth factor on the division and fusion of bovine myoblasts.
Gospodarowicz, D., Weseman, J., Moran, J. S., & Lindstrom, J. M. (1976) · The Journal of Cell Biology · doi:10.1083/jcb.70.2.395 · Cited by 189 · see citing works
“ated myotubes) in both chick myoblasts (5) and the L6 cell line ( 25 ), we have not observed such an effect of insulin using primary cultures of bovine myoblasts.”
BackgroundEffects of the somatomedins and insulin on myoblast differentiation in vitro
Ewton, D. Z., & Florini, J. R. (1981) · Developmental Biology · doi:10.1016/0012-1606(81)90312-2 · Cited by 188 · see citing works
Biphasic concentration dependency of stimulation of myoblast differentiation by somatomedins
Florini, J. R., Ewton, D. Z., Falen, S. L., & Wyk, J. J. V. (1986) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1986.250.5.c771 · Cited by 179 · see citing works
Therapeutic approaches for muscle wasting disorders
Lynch, G. S., Schertzer, J. D., & Ryall, J. G. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.11.004 · Cited by 152 · see citing works
Muscle stem cell isolation and in vitro culture for meat production: A methodological review
Choi, K., Yoon, J. W., Kim, M., Lee, H. J., Jeong, J., Ryu, M., Jo, C., & Lee, C. (2020) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12661 · Cited by 146 · see citing works
Allen, R. E., Dodson, M. V., & Luiten, L. S. (1984) · Experimental Cell Research · doi:10.1016/0014-4827(84)90239-8 · Cited by 140 · see citing works
Developmental pattern of mouse skeletal myosin heavy chain gene transcripts in vivo and in vitro
Weydert, A., Barton, P. J. R., Harris, A., Pinset, C., & BUCKINGHAM, M. E. (1987) · Cell · doi:10.1016/0092-8674(87)90762-8 · Cited by 124 · see citing works
Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis
Khandjian, E. W. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.13.2121 · Cited by 114 · see citing works
“2% dextrancoated charcoal-treated FBS and 10 –6 M insulin (18).”
BackgroundA serum-free medium for the growth of muscle cells in culture
Florini, J. R., & Roberts, S. B. (1979) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/bf02619157 · Cited by 102 · see citing works
Somers, D. G., Pearson, M. L., & Ingles, C. J. (1975) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)41243-x · Cited by 101 · see citing works
Self-citationPinset, C., Montarras, D., Chenevert, J. M., Minty, A. J., Barton, P. J. R., Laurent‐Winter, C., & Gros, F. (1988) · Differentiation · doi:10.1111/j.1432-0436.1988.tb00588.x · Cited by 88 · see citing works
Induction of sugar uptake response to insulin by serum depletion in fusing L6 myoblasts
Klip, A., Li, G., & Logan, W. J. (1984) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1984.247.3.e291 · Cited by 84 · see citing works
Kraft, T. F. B., Dey, M., Rogers, R. B., Ribnicky, D., Gipp, D. M., Cefalu, W. T., Raskin, I., & Lila, M. A. (2008) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf071999d · Cited by 83 · see citing works
“L6 culture was performed as described by Mandel and Pearson (34).”
BackgroundBèguinot, F., Kahn, C. R., Moses, A. C., & Smith, R. J. (1986) · Endocrinology · doi:10.1210/endo-118-1-446 · Cited by 81 · see citing works
Ahmad, S. S., Chun, H. J., Ahmad, K., Shaikh, S., Lim, J. H., Ali, S. M., Han, S. S., Hur, S. J., Sohn, J., Lee, E. J., et al. (2022) · Journal of Animal Science and Technology · doi:10.5187/jast.2022.e114 · Cited by 78 · see citing works
Identification of Differentially Regulated Secretome Components During Skeletal Myogenesis
Chan, C. Y. X., Masui, O., Krakovska, O., Belozerov, V. E., Voisin, S. N., Ghanny, S., Chen, J., Dharsee, M., Zhu, P., Evans, K., et al. (2011) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m110.004804 · Cited by 69 · see citing works
Isolation of satellite cells from ovine skeletal muscles
Dodson, M. V., McFarland, D. C., Martin, E., & Brannon, M. A. (1986) · Methods in Cell Science · doi:10.1007/bf01404483 · Cited by 60 · see citing works
“Numerous reports have described proliferative and differentiative properties of embryonic myogenic cells (5, 10-12 ,14-17), neonatal myogenic cells {7), and clonomyogenic cells (8,9~ in vitro.”
BackgroundA synergistic effect of glucocorticoids and insulin on the differentiation of myoblasts
Ball, E. H., & Sanwal, B. D. (1980) · Journal of Cellular Physiology · doi:10.1002/jcp.1041020105 · Cited by 59 · see citing works
Montarras, D., Aurade, F., Johnson, T. R., Ilan, J., Gros, F., & Pinset, C. (1996) · Journal of Cell Science · doi:10.1242/jcs.109.3.551 · Cited by 58 · see citing works
PHYSIOLOGY AND ENDOCRINOLOGY SYMPOSIUM: Roles for insulin-supported skeletal muscle growth1,2
Rhoads, R. P., Baumgard, L. H., El‐Kadi, S. W., & Zhao, L. D. (2016) · Journal of Animal Science · doi:10.2527/jas.2015-0110 · Cited by 56 · see citing works
“The physiological effects of insulin have been studied in satellite cells of rodents (de la Haba et al., 1966; Mandel and Pearson, 1974; Allen et al., 1985; Illario et al., 2009), cattle (Cassar-Malek et al., 1999), and fish (Castillo et al., 2004).”
Synergistic Influence of Polypeptide Growth Factors on Cultured Human Muscle
Askanas, V., & Gallez-Hawkins, G. M. (1985) · Archives of Neurology · doi:10.1001/archneur.1985.04210090013004 · Cited by 56 · see citing works
Insulin acts as a somatomedin analog in stimulating myoblast growth in serum-free medium
Florini, J. R., & Ewton, D. Z. (1981) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/bf02618442 · Cited by 56 · see citing works
Targeting of skeletal muscle in vitro using biotinylated immunoliposomes
Schnyder, A., Krähenbühl, S., Török, M., Drewe, J., & Huwyler, J. (2004) · Biochemical Journal · doi:10.1042/bj20031034 · Cited by 54 · see citing works
Induction of muscle genes in neural cells.
Wright, W. E. (1984) · The Journal of Cell Biology · doi:10.1083/jcb.98.2.427 · Cited by 54 · see citing works
The Role of the IGFs in Myogenic Differentiation
Magri, K. A., Ewton, D. Z., & Florini, J. R. (1991) · Advances in experimental medicine and biology · doi:10.1007/978-1-4684-5949-4_6 · Cited by 49 · see citing works
Exercise-Induced Hormonal Changes and their Effects upon Skeletal Muscle Tissue
Deschenes, M. R., Kraemer, W. J., Maresh, C. M., & Crivello, J. F. (1991) · Sports Medicine · doi:10.2165/00007256-199112020-00002 · Cited by 48 · see citing works
Anabolic effect of plant brassinosteroid
Esposito, D., Komarnytsky, S., Shapses, S., & Raskin, I. (2011) · The FASEB Journal · doi:10.1096/fj.11-181271 · Cited by 44 · see citing works
“After 7–9 d of culture, the myoblasts had fused into multinucleated myotubes (31).”
BackgroundHuang, D., & Cuatrecasas, P. (1975) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)40844-2 · Cited by 45 · see citing works
Myogenesis of avian striated muscle in vitro: role of collagen in myofiber formation.
Haba, G. D. L., Kamali, H. M., & Tiede, D. M. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.7.2729 · Cited by 42 · see citing works
“cent report, Mandel and Pearson (2) have also demonstrated that insulin can support myogenesis of rat myoblasts.”
BackgroundInfluentialGoto, S., Miyazaki, K., Funabiki, T., & Yasumitsu, H. (1999) · Analytical Biochemistry · doi:10.1006/abio.1999.4163 · Cited by 41 · see citing works
Amanitin binding to RNA polymerase II in α-amanitin-resistant rat myoblast mutants
Crerar, M. M., Andrews, S. J., David, E. S., Somers, D. G., Mandel, J., & Pearson, M. L. (1977) · Journal of Molecular Biology · doi:10.1016/s0022-2836(77)80147-2 · Cited by 38 · see citing works
Self-citationRodgers, K., Arvidson, C. G., & Melville, S. B. (2011) · Infection and Immunity · doi:10.1128/iai.00909-10 · Cited by 37 · see citing works
“For C2C12 myoblasts (46) and L6 myoblasts (22), cells were seeded into”
AICAR and hyperosmotic stress increase insulin-stimulated glucose transport
Smith, J. L., Patil, P. B., & Fisher, J. S. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01297.2004 · Cited by 36 · see citing works
“Insulin was included in the initial differentiation medium, because it has been reported that insulin stimulates myogenesis in L6 and C2C12 myoblasts (26, 41).”
BackgroundGhanim, H., Dhindsa, S., Batra, M., Green, K., Abuaysheh, S., Kuhadiya, N. D., Makdissi, A., Chaudhuri, A., Sandhu, S., & Dandona, P. (2019) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgz288 · Cited by 32 · see citing works
FOXO1 and GSK-3β Are Main Targets of Insulin-Mediated Myogenesis in C2C12 Muscle Cells
Litwiniuk, A., Pijet, B., Pijet-Kucicka, M., Gajewska, M., Pająk, B., & Orzechowski, A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146726 · Cited by 32 · see citing works
Makman, M. H., Morris, S. A., & Ahn, H. S. (1977) · Elsevier eBooks · doi:10.1016/b978-0-12-598303-7.50014-x · Cited by 32 · see citing works
Parfett, C. L. J., Jamieson, J., & Wright, J. R. (1981) · Experimental Cell Research · doi:10.1016/0014-4827(81)90032-x · Cited by 31 · see citing works
In Vitro effects of thyroxine and insulin on myoblasts from chick embryo skeletal muscle
Kumegawa, M., Ikeda, E., Hosoda, S., & Takuma, T. (1980) · Developmental Biology · doi:10.1016/0012-1606(80)90134-7 · Cited by 31 · see citing works
Documenting GLUT4 Exocytosis and Endocytosis in Muscle Cell Monolayers
Ishikura, S., Antonescu, C. N., & Klip, A. (2010) · Current Protocols in Cell Biology · doi:10.1002/0471143030.cb1515s46 · Cited by 30 · see citing works
“L6 cells are originally derived from rat skeletal muscle, and propagate as mononucleated myoblasts, but differentiate into multinucleated myotubes upon incubation in low-serumcontaining medium (Yaffe, 1968; Richler and Yaffe, 1970; Mandel and Pearson, 1974; Yaffe and Saxel, 1977).”
BackgroundRidpath, J. F., Huiatt, T. W., Trenkle, A. H., Robson, R. M., & Bechtel, P. J. (1984) · Differentiation · doi:10.1111/j.1432-0436.1984.tb01384.x · Cited by 30 · see citing works
Ontogeny of insulin binding during chick skeletal myogenesis in vitro
Sandra, A., & Przybylski, R. J. (1979) · Developmental Biology · doi:10.1016/0012-1606(79)90225-2 · Cited by 29 · see citing works
Insulin binding by a cell line (HT 29) derived from human colonic cancer
Forgue-Lafitte, M. E., Horvat, A., & Rosselin, G. (1979) · Molecular and Cellular Endocrinology · doi:10.1016/0303-7207(79)90100-x · Cited by 28 · see citing works
Lynes, M. D., Schulz, T. J., Pan, A. J., & Tseng, Y. (2015) · Endocrinology · doi:10.1210/en.2014-1773 · Cited by 27 · see citing works
“Insulin is known to regulate both cell growth and differentiation in many cell types, including muscle (34), mammary gland (35), adipose (36) and others.”
BackgroundInduction of myogenic differentiation in serum-free medium does not require DNA synthesis
Pinset, C., & Whalen, R. G. (1985) · Developmental Biology · doi:10.1016/0012-1606(85)90032-6 · Cited by 26 · see citing works
Wright, W. E. (1984) · The Journal of Cell Biology · doi:10.1083/jcb.98.2.436 · Cited by 25 · see citing works
Insulin and Analogue Effects on Protein Degradation in Different Cell Types
Fawcett, J., Hamel, F. G., Bennett, R. G., Vajó, Z., & Duckworth, W. C. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m007988200 · Cited by 25 · see citing works
Cell surface changes accompanying myoblast differentiation
Furcht, L. T., Wendelschafer‐Crabb, G., & Woodbridge, P. (1977) · Journal of Supramolecular Structure · doi:10.1002/jss.400070305 · Cited by 25 · see citing works
Logan, W. J., Klip, A., & Gagalang, E. (1982) · Journal of Cellular Physiology · doi:10.1002/jcp.1041120211 · Cited by 24 · see citing works
Esposito, D., Rathinasabapathy, T., Poulev, A., Komarnytsky, S., & Raskin, I. (2011) · Journal of Medicinal Chemistry · doi:10.1021/jm200028h · Cited by 22 · see citing works
Sandra, A., Leon, M. A., & Przybylski, R. J. (1979) · Endocrinology · doi:10.1210/endo-105-2-391 · Cited by 22 · see citing works
Gene expression during the differentiation of myogenic cells of the L6 line
Wahrmann, J. P., Drugeon, G., Delain, E., & Delain, D. (1976) · Biochimie · doi:10.1016/s0300-9084(76)80225-8 · Cited by 21 · see citing works
Influence of external diffusible factors on myogenesis of the cells of the line L
Delain, D., Wahrmann, J. P., & Gros, F. (1981) · Experimental Cell Research · doi:10.1016/0014-4827(81)90421-3 · Cited by 21 · see citing works
Gong, Y.-Y., Liu, Y.-Y., Li, J., Su, L., Yu, S., Zhu, X.-N., Cao, X.-P., & Xiao, H.-P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113784 · Cited by 20 · see citing works
“Rat L6 skeletal muscle cells (Institute of Materia Medica, Shanghai, China) were grown in high glucose DMEM containing 4500 mg/L D-glucose, 10% fetal bovine serum (FBS), 100 U/ml penicillin, 100 mg/ml streptomycin (Invitrogen, Grand Island, NY, USA) until 40% confluent and then altered with differentiating media (2% F…”
MethodPerkins, R., & Scott, R. E. (1978) · Lipids · doi:10.1007/bf02533724 · Cited by 17 · see citing works
Schudt, C., & Pette, D. (1978) · Advances in Enzyme Regulation · doi:10.1016/0065-2571(78)90070-5 · Cited by 16 · see citing works
Wright, W. E., & Aronoff, J. (1983) · The Journal of Cell Biology · doi:10.1083/jcb.96.6.1571 · Cited by 16 · see citing works
“The ceils could be stimulated to differentiate at subcomquent densities if they were downshified to a medium containing 1% NBS and 5/~g/ml insulin ( 21 ).”
BackgroundCrerar, M. M., Leather, R. A., David, E. S., & Pearson, M. L. (1983) · Molecular and Cellular Biology · doi:10.1128/mcb.3.5.946-955.1983 · Cited by 14 · see citing works
Self-citationA Glance into the Near Future: Cultivated Meat from Mammalian and Insect Cells
Giglio, F., Scieuzo, C., Ouazri, S., Pucciarelli, V., Ianniciello, D., Letcher, S. M., Salvia, R., Laginestra, A., Kaplan, D. L., & Falabella, P. (2024) · Small Science · doi:10.1002/smsc.202400122 · Cited by 13 · see citing works
Propriétés des fibres musculaires squelettiques. II. Influences hormonales
Vigneron, P., Dainat, J., & Bacou, F. (1989) · annales de biologie animale biochimie biophysique · doi:10.1051/rnd:19890102 · Cited by 13 · see citing works
Characterization of the Inhibition of Protein Degradation by Insulin in L6 Cells
Fawcett, J., Hamel, F. G., & Duckworth, W. C. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2000.2160 · Cited by 13 · see citing works
Dhindsa, S., Ghanim, H., Green, K., Abuaysheh, S., Batra, M., Makdissi, A., Chaudhuri, A., Sandhu, S., & Dandona, P. (2019) · European Journal of Endocrinology · doi:10.1530/eje-19-0514 · Cited by 10 · see citing works
Cloning of Contractile Protein Genes
Schwartz, R. J., & Stone, E. M. (1983) · Springer eBooks · doi:10.1007/978-1-4615-9296-9_7 · Cited by 10 · see citing works
The amplified expression of factors regulating myogenesis in L6 myoblasts.
Wright, W. E. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.100.1.311 · Cited by 9 · see citing works
“Clones containing a chromosome number appropriate for hybrids between the parental cells were then replated at clonal density and allowed to grow for 2 wk to form large colonies, then stimulated to differentiate by feeding with medium containing I% fetal bovine serum and 5 ~g/ml insulin (12).”
The INSR/AKT/mTOR pathway regulates the pace of myogenesis in a syndecan-3-dependent manner
Jones, F. K., Phillips, A. M., Jones, A. R., & Pisconti, A. (2022) · Matrix Biology · doi:10.1016/j.matbio.2022.09.004 · Cited by 7 · see citing works
Scott, R. E. (1978) · Cell Differentiation · doi:10.1016/0045-6039(78)90033-7 · Cited by 7 · see citing works
The BrdU content of DNA is decreased during reversal of inhibition of myogenesis by deoxycytidine
Wright, W. E. (1982) · Somatic Cell and Molecular Genetics · doi:10.1007/bf01542850 · Cited by 7 · see citing works
Huang, F. L., & Tao, S.-H. (1980) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(80)90264-7 · Cited by 6 · see citing works
Goff, M., & Chen, G. (2020) · Biochemistry and Cell Biology · doi:10.1139/bcb-2020-0131 · Cited by 5 · see citing works
“Insulin has been shown to enhance fusion of myoblast into myotubes and activity of creatine kinase in L6 cells (Mandel and Pearson 1974).”
BackgroundVandoolaeghe, P., Gueuning, M.-A., & Rousseau, G. G. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.0767 · Cited by 5 · see citing works
Kamely, D. (1977) · Journal of Cellular Physiology · doi:10.1002/jcp.1040900209 · Cited by 5 · see citing works
Measurement of GLUT4 Traffic to and from the Cell Surface in Muscle Cells
Antonescu, C. N., Ishikura, S., Bilan, P. J., & Klip, A. (2023) · Current Protocols · doi:10.1002/cpz1.803 · Cited by 4 · see citing works
“…derived from rat skeletal muscle, propagate as mononucleated myoblasts, and differentiate into multinucleated myotubes upon incubation in low-serumcontaining medium (Mandel & Pearson, 1974; Richler & Yaffe, 1970; Yaffe, 1968; Yaffe & Saxel, 1977a, b) but do not form actomyosin cross-striations.”
BackgroundJones, F. K., Phillips, A. M., Jones, A. R., & Pisconti, A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.10.244152 · Cited by 4 · see citing works
“It appears to promote 68 both myoblast proliferation and differentiation (Conejo et al., 2001; Grabiec et al., 2014; Grzelkowska69 Kowalczyk et al., 2013; Mandel and Pearson, 1974).”
BackgroundProliferation of Myocytes on Different ECM-Components of Animal/Human Origin in Vitro
Falkner, E., Kapeller, B., Eberl, H. C., Frick, W. E., Losert, U. M., & Macfelda, K. (2003) · The International Journal of Artificial Organs · doi:10.1177/039139880302600610 · Cited by 3 · see citing works
“thigh muscle origin (5) were used in proliferation assays to evaluate the different extracellular matrices.”
MethodExperimental Validation of an In Vitro Method for Assessing Insulin-Dependent Glucose Uptake
Afanaseva, A. N., Saparova, V. B., Макаренко, И. Е., Васильевич, Д. Р., & Selmenskikh, T. A. (2022) · The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products Regulatory Research and Medicine Evaluation · doi:10.30895/1991-2919-2022-398 · Cited by 2 · see citing works
Kumegawa, M., Takuma, T., Hosoda, S., & Nakanishi, M. (1979) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(79)90216-2 · Cited by 2 · see citing works
CHICK BRAIN CREATINE KINASE ONTOGENY BEFORE THE ADVENT OF CREATINE AND INSULIN
Ramírez, O., TAKAHASHI, J., & Hernández, M. M. G. (1977) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1977.tb07762.x · Cited by 2 · see citing works
"In vitro" and "in vivo" drug targeting using biotinylated immunoliposomes
Schnyder, A. (2005) · edoc (University of Basel) · doi:10.5451/unibas-003930401 · Cited by 1 · see citing works
“CRL-1458) (Mandel and Pearson, 1974) were obtained from ATCC (Manassas, VA) and were grown using Dulbecco's Modified Eagle Medium (DMEM, Gibco-BRL) supplemented with 4 mM L-glutamine, 1.0 mM sodium pyruvate, 4.5 g/L glucose, 1.5 g/L sodium bicarbonate, 10 % heat-inactivated fetal calf serum (FCS),…”
MethodInfluentialCrerar, M. M., Leather, R., David, E. S., & Pearson, M. L. (1983) · Molecular and Cellular Biology · doi:10.1128/mcb.3.5.946 · Cited by 1 · see citing works
Self-citationRamı́rez, O., & Alemán, V. (1986) · Journal of Experimental Zoology · doi:10.1002/jez.1402380108
Ramanathan, M., Chinniah, V., & Maida Engels, S. E. (2024) · Journal of Natural Remedies · doi:10.18311/jnr/2024/43768
Zheng, L., Cherry, Z. K., Soltys, G., Penner, M., Samuell, N., Welivita, D., Thomas, B., Fisher, J. S., & Wang, Y. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.111402
“Notably, lipoamide abolishes the effect of curcumin on p38 in L6 cells, which are a cell line derived from rat skeletal muscle (26) and known to induce p38 activation by curcumin (27).”
- Authors
- MANDEL, J.-L., & PEARSON, M. L.
- Affiliations
- University of Toronto (CA)
- ORCID
- MANDEL, JEAN-LOUIS
- Venue
- Nature
- Published
- 1974-10
- Volume
- 251
- Issue
- 5476
- Pages
- 618-620
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1994361005
- Cited by
- 84
- References
- 17
- Citations by year
- 2026: 1 · 2024: 2 · 2023: 1 · 2022: 3 · 2020: 2 · 2019: 2 · 2016: 2 · 2015: 1 · 2014: 1
- FWCI
- 2.09
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Keywords
- insulin, myogenesis, L6 myoblasts, myoblast fusion, multinucleated myotubes, cyclic AMP, adenylate cyclase, creatine kinase, myosin, serum requirement
- MeSH terms
- Animals, Cell Differentiation, Cell Fusion, Cell Line, Creatine Kinase, Insulin, Morphogenesis, Muscles, Stimulation, Chemical, Rats
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