TY - JOUR
T1 - Transferrin receptor numbers and transferrin and iron uptake in cultured chick muscle cells at different stages of development
AU - Sorokin, L. M.
AU - Morgan, E. H.
AU - Yeoh, G. C.T.
PY - 1987/1/1
Y1 - 1987/1/1
N2 - The mechanism of iron uptake and the changes which occur during cellular development of muscle cells were investigated using primary cultures of chick embryo breast muscle. Replicating presumptive myoblasts were examined in exponential growth and after growth had plateaued. These were compared to the terminally differentiated cell type, the myotube. All cells, regardless of the state of growth or differentiation, had specific receptors for transferrin. Presumptive myoblasts in exponential growth had more transferrin receptors (3.78 ± 0.24 × 1010 receptors/μg DNA) than when division had ceased (1.70 ± 0.14 × 1010 receptors/μg DNA), while myotubes had 3.80 ± 0.26 × 1010 receptors/μg DNA. Iron uptake occurred by receptor‐mediated endocytosis of transferrin. While iron was accumulated by the cells, apotransferrin was released in an undegraded form. There was a close correlation between the molar rates of endocytosis of transferrin and iron. Maximum rates of iron uptake were significantly higher in myotubes than in presumptive myoblasts in either exponential growth or after growth had plateaued. There were two rates of exocytosis of transferrin, implying the existence of two intracellular pathways for transferrin. These experiments demonstrate that iron uptake by muscle cells in culture occurs by receptor‐mediated endocytosis of transferrin and that transferrin receptor numbers and the kinetics of transferrin and iron uptake vary with development of the cells.
AB - The mechanism of iron uptake and the changes which occur during cellular development of muscle cells were investigated using primary cultures of chick embryo breast muscle. Replicating presumptive myoblasts were examined in exponential growth and after growth had plateaued. These were compared to the terminally differentiated cell type, the myotube. All cells, regardless of the state of growth or differentiation, had specific receptors for transferrin. Presumptive myoblasts in exponential growth had more transferrin receptors (3.78 ± 0.24 × 1010 receptors/μg DNA) than when division had ceased (1.70 ± 0.14 × 1010 receptors/μg DNA), while myotubes had 3.80 ± 0.26 × 1010 receptors/μg DNA. Iron uptake occurred by receptor‐mediated endocytosis of transferrin. While iron was accumulated by the cells, apotransferrin was released in an undegraded form. There was a close correlation between the molar rates of endocytosis of transferrin and iron. Maximum rates of iron uptake were significantly higher in myotubes than in presumptive myoblasts in either exponential growth or after growth had plateaued. There were two rates of exocytosis of transferrin, implying the existence of two intracellular pathways for transferrin. These experiments demonstrate that iron uptake by muscle cells in culture occurs by receptor‐mediated endocytosis of transferrin and that transferrin receptor numbers and the kinetics of transferrin and iron uptake vary with development of the cells.
UR - http://www.scopus.com/inward/record.url?scp=0023187804&partnerID=8YFLogxK
U2 - 10.1002/jcp.1041310306
DO - 10.1002/jcp.1041310306
M3 - Article
C2 - 3597543
AN - SCOPUS:0023187804
SN - 0021-9541
VL - 131
SP - 342
EP - 353
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 3
ER -