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Irreversible reduction in potassium fluxes accompanies terminal differentiation of human myoblasts to myotubes
Author(s) -
Panet Rivka,
Digregorio Debra M.,
Brown Robert H.
Publication year - 1987
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041320108
Subject(s) - myogenesis , terminal (telecommunication) , reduction (mathematics) , myocyte , chemistry , potassium , microbiology and biotechnology , biophysics , biochemistry , biology , computer science , telecommunications , mathematics , organic chemistry , geometry
Potassium and sodium fluxes believed to be important in the cellular response to serum and growth factors have not been widely investigated in cells which have undergone terminal differentiation. In this study we have analyzed two main K + transport systems—the ouabain‐sensitive Na + /K + pump and the bumetanide‐sensitive transporter—in human muscle in vitro at two developmental stages: proliferating myoblasts and differentiated myotubes. Myoblast differentiation to myotubes was accompanied by a marked decrease in both the ouabain‐sensitive and the bumetanide‐sensitive K + (Rb + ) influxes. The addition of serum to the terminally differentiated myotubes had no effect on these K + transporters. However, serum addition to serum‐deprived, undifferentiated myoblasts produced a marked stimulation of these K + fluxes. The bumetanide‐sensitive K + transporter in human myoblasts and myotubes has the following properties: (1) It carries 30% and 40% of the total K + influx in myoblasts and myotubes, respectively. (2) It performs net efflux of K + in the undifferentiated myoblasts and zero net flux (self‐exchange) in terminally differentiated myotubes. (3) It is dependent on extracellular Na + and Cl − in addition to K + . (4) In myoblasts, the Km value for K + is 1.36 mM, similar to the Km for K + of the Na + /K + pump. (5) It is resistant to ouabain (up to 2 mM) and sensitive to furosemide (K 0.5 = 5 × 10 −6 M) and bumetanide (K 0.5 = 10 −7 M). These data indicate that following terminal differentiation of proliferating myoblasts to mitotically inactive myotubes there is an irreversible reduction of K + fluxes with a change in the net flux of K + carried by the bumetanide‐sensitive transporter.