Comparison of Growth Factor Receptors and Metabolic Characteristics of Satellite Cells Derived from the Biceps Femoris and Pectoralis Major Muscles of the Turkey

McFarland, Douglas C.; Gilkerson, Kysa K.; Pesall, Jane E.; Wellenreiter, R. H.; Ferrin, Neal H.; Ye, W.V.; Yun, Yong Soo; Wal, L.S.Vander

doi:10.1006/gcen.1996.6806

Cited by 9 publications

(6 citation statements)

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“…These findings were in agreement with the results obtained by McFarland et al (1997a). On the other hand, the observations seen with turkey BF and PM satellite cells, in which PM satellite cells were more responsive to the mitogenic effects of serum (McFarland et al, 1995), were in contrast to the results obtained from the present and previous (McFarland et al, 1997b) experiments. The reasons for these differences between species remain unclear.…”

Section: Discussioncontrasting

confidence: 91%

Temporal expression of growth factor genes during myogenesis of satellite cells derived from the biceps femoris and pectoralis major muscles of the chicken

2000

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The expression of mRNAs for transforming growth factors (TGF-beta2, myostatin, activin-B, and follistatin), insulin-like growth factors (IGF-I and -II), and fibroblast growth factor (basic, bFGF) was investigated in satellite cells derived from chicken pectoralis major (PM) and biceps femoris (BF) muscles in the stages from initiation of proliferation to fusion. These growth factor gene cDNAs were synthesized by reverse transcriptase polymerase chain reaction (RT-PCR). No myostatin, activin-B, follistatin or bFGF expression was detected in either cell culture at 0 h. TGF-beta2 mRNA level increased at 48 h (P < 0.01) and remained constant through 144 h in both PM and BF satellite cell cultures. The ontogeny of myostatin gene expression with the exception of a sharp increase in BF culture at 72 h (P < 0.01), was nearly identical in both cell cultures. Activin-B mRNA level in PM satellite cells was higher than that in BF satellite cells at 72 h and 120 h (P < 0.01). Follistatin mRNA in PM satellite cells was higher than that in BF satellite cells at 24, 96, and 120 h culture (P < 0.01). No IGF-I gene expression was detected in cell cultures at any time point. IGF-II gene expression in BF satellite cells declined at 96 h (P < 0.01) and remained reduced until 144 h. bFGF mRNA in both satellite cell cultures increased at 24 h (P < 0.05) and remained at this level in BF satellite cells through 144 h.

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Section: Discussioncontrasting

confidence: 91%

Temporal expression of growth factor genes during myogenesis of satellite cells derived from the biceps femoris and pectoralis major muscles of the chicken

2000

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“…Satellite cells have a tremendous proliferative capacity and are thought to bear a tissue‐specific capacity for proliferation and induction of muscle fiber hypertrophy (Machida and Booth, 2004). It has been reported that satellite cells derived from chicken slow muscle fiber proliferated at a greater rate than fast muscle cells when placed in the presence of a mitogenic serum (McFarland et al, 1997b; Kocamis et al, 2001). We further compared the satellite cells' activation frequency between the breast muscle and leg muscle of ducks and found that IGF‐1 played more roles involved in satellite cell activation derived from leg muscle than from breast muscle (Fig.…”

Section: Discussionmentioning

confidence: 99%

In ovo feeding of IGF‐1 to ducks influences neonatal skeletal muscle hypertrophy and muscle mass growth upon satellite cell activation

Liu

Wang

Zhang

et al. 2012

Journal Cellular Physiology

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To investigate reasons for the muscle increase observed when eggs are treated by IGF-1 and whether or not satellite cell activation is specific to different types of myofibers, duck eggs were administrated with IGF-1. After injection, during the neonatal stages, the duck breast muscle and leg muscle were isolated for analysis. The muscle weight, muscle fiber diameter (MFD), cross-sectional area (CSA), the number of myofibers per unit area (MFN) and frequency of satellite cell activation and mitosis at the embryo stage of 27 days (27E) and the postnatal stage of 2 days after hatching (P2D) were determined. In addition, expression of two important myogenic transcription factors MyoD and Myf5 were detected and compared in the two types of muscle tissues. Results indicated that IGF-1 administration increased the duck body weight, MFD, CSA, MFN, and quantity of activated satellite cells and mitotic nuclei in the two types of muscle tissues. The MyoD and Myf5 expressed at a higher level in IGF-1-treated muscle. IGF-1 stimulated muscle weight growth more in the leg muscle than in the breast muscle. These results indicate that in ovo feeding of IGF-1 can stimulate duck growth and, especially, lead to increased muscle hypertrophy. These increases appear to be mainly dependent on the activation of satellite cells, some of which proliferate and fuse to the myofiber, enabling increased muscle mass. IGF-1 can indirectly affect satellite cells by regulating the expression of two important myogenic transcription factors, MyoD and Myf5, which help activate satellite cells.

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“…Differences between these two types of satellite cells are mirrored also by other properties, e.g., their different MHC isoform patterns (this study and [10]). Different responsiveness to platelet-derived growth factor (PDGF) of satellite cells from "red" and "white" muscle fibres from turkey has been shown [28].…”

Section: Discussionmentioning

confidence: 99%

Evidence that acidic fibroblast growth factor promotes maturation of rat satellite-cell-derived myotubes in vitro

Düsterhöft

Pette

1999

Differentiation

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Comparison of Growth Factor Receptors and Metabolic Characteristics of Satellite Cells Derived from the Biceps Femoris and Pectoralis Major Muscles of the Turkey

Cited by 9 publications

References 0 publications

Temporal expression of growth factor genes during myogenesis of satellite cells derived from the biceps femoris and pectoralis major muscles of the chicken

Temporal expression of growth factor genes during myogenesis of satellite cells derived from the biceps femoris and pectoralis major muscles of the chicken

In ovo feeding of IGF‐1 to ducks influences neonatal skeletal muscle hypertrophy and muscle mass growth upon satellite cell activation

Evidence that acidic fibroblast growth factor promotes maturation of rat satellite-cell-derived myotubes in vitro

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