Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1998 Oct;75(4):1926–1934. doi: 10.1016/S0006-3495(98)77633-7

MgADP promotes a catch-like state developed through force-calcium hysteresis in tonic smooth muscle.

A Khromov 1, A V Somlyo 1, A P Somlyo 1
PMCID: PMC1299863  PMID: 9746533

Abstract

Tonic rabbit femoral artery and phasic rabbit ileum smooth muscles permeabilized with Triton X-100 were activated either by increasing [Ca2+] from pCa > 8.0 to pCa 6.0 (calcium-ascending protocol) or contracted at pCa 6.0 before lowering [Ca2+] (calcium-descending protocol). The effects of, respectively, high [MgATP]/low [MgADP] [10 mM MgATP + creatine phosphate (CP) + creatine kinase (CK)] or low [MgATP]/[MgADP] (2 mM MgATP, 0 CP, 0 CK) on the "force-[Ca]" relationships were determined. In femoral artery at low, but not at high, [MgATP]/[MgADP] the force and the ratio of stiffness/force at pCa 7.2 were significantly higher under the calcium-descending than calcium-ascending protocols (54% vs. 3% of Po, the force at pCa 6.0) (force hysteresis); the levels of regulatory myosin light chain (MLC20) phosphorylation (9 +/- 2% vs. 10 +/- 2%) and the velocities of unloaded shortening V0 (0.02 +/- 0.004 l/s with both protocols) were not significantly different. No significant force hysteresis was detected in rabbit ileum under either of these experimental conditions. [MgADP], measured in extracts of permeabilized femoral artery strips by two methods, was 130-140 microM during maintained force under the calcium-descending protocol. Exogenous CP (10 mM) applied during the descending protocol reduced endogenous [MgADP] to 46 +/- 10 microM and abolished force hysteresis: residual force at low [Ca2+] was 17 +/- 5% of maximal force. We conclude that the proportion of force-generating nonphosphorylated (AMdp) relative to phosphorylated cross-bridges is higher on the Ca2+-descending than on the Ca2+-ascending force curve in tonic smooth muscle, that this population of positively strained dephosphorylated cross-bridges has a high affinity for MgADP, and that the dephosphorylated AMdp . MgADP state makes a significant contribution to force maintenance at low levels of MLC20 phosphorylation.

Full Text

The Full Text of this article is available as a PDF (105.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arner A., Hellstrand P. Effects of calcium and substrate on force-velocity relation and energy turnover in skinned smooth muscle of the guinea-pig. J Physiol. 1985 Mar;360:347–365. doi: 10.1113/jphysiol.1985.sp015621. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Butler T. M., Siegman M. J., Mooers S. U. Slowing of crossbridge cycling rate in mammalian smooth muscle occurs without evidence of an increase in internal load. Prog Clin Biol Res. 1987;245:289–301. [PubMed] [Google Scholar]
  3. Chase P. B., Kushmerick M. J. Effect of physiological ADP concentrations on contraction of single skinned fibers from rabbit fast and slow muscles. Am J Physiol. 1995 Feb;268(2 Pt 1):C480–C489. doi: 10.1152/ajpcell.1995.268.2.C480. [DOI] [PubMed] [Google Scholar]
  4. Clark J. F., Dillon P. F. Phosphocreatine and creatine kinase in energetic metabolism of the porcine carotid artery. J Vasc Res. 1995 Jan-Feb;32(1):24–30. doi: 10.1159/000159074. [DOI] [PubMed] [Google Scholar]
  5. Clark J. F., Kemp G. J., Radda G. K. The creatine kinase equilibrium, free [ADP] and myosin ATPase in vascular smooth muscle cross-bridges. J Theor Biol. 1995 Mar 21;173(2):207–211. doi: 10.1006/jtbi.1995.0056. [DOI] [PubMed] [Google Scholar]
  6. Cohen D. M., Murphy R. A. Differences in cellular contractile protein contents among porcine smooth muscles: evidence for variation in the contractile system. J Gen Physiol. 1978 Sep;72(3):369–380. doi: 10.1085/jgp.72.3.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cooke R., Pate E. The effects of ADP and phosphate on the contraction of muscle fibers. Biophys J. 1985 Nov;48(5):789–798. doi: 10.1016/S0006-3495(85)83837-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cremo C. R., Geeves M. A. Interaction of actin and ADP with the head domain of smooth muscle myosin: implications for strain-dependent ADP release in smooth muscle. Biochemistry. 1998 Feb 17;37(7):1969–1978. doi: 10.1021/bi9722406. [DOI] [PubMed] [Google Scholar]
  9. Dillon P. F., Aksoy M. O., Driska S. P., Murphy R. A. Myosin phosphorylation and the cross-bridge cycle in arterial smooth muscle. Science. 1981 Jan 30;211(4481):495–497. doi: 10.1126/science.6893872. [DOI] [PubMed] [Google Scholar]
  10. Edman K. A. The velocity of unloaded shortening and its relation to sarcomere length and isometric force in vertebrate muscle fibres. J Physiol. 1979 Jun;291:143–159. doi: 10.1113/jphysiol.1979.sp012804. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Fuglsang A., Khromov A., Török K., Somlyo A. V., Somlyo A. P. Flash photolysis studies of relaxation and cross-bridge detachment: higher sensitivity of tonic than phasic smooth muscle to MgADP. J Muscle Res Cell Motil. 1993 Dec;14(6):666–677. doi: 10.1007/BF00141563. [DOI] [PubMed] [Google Scholar]
  12. Gollub J., Cremo C. R., Cooke R. ADP release produces a rotation of the neck region of smooth myosin but not skeletal myosin. Nat Struct Biol. 1996 Sep;3(9):796–802. doi: 10.1038/nsb0996-796. [DOI] [PubMed] [Google Scholar]
  13. Gong M. C., Cohen P., Kitazawa T., Ikebe M., Masuo M., Somlyo A. P., Somlyo A. V. Myosin light chain phosphatase activities and the effects of phosphatase inhibitors in tonic and phasic smooth muscle. J Biol Chem. 1992 Jul 25;267(21):14662–14668. [PubMed] [Google Scholar]
  14. Hellstrand P., Paul R. J. Phosphagen content, breakdown during contraction, and O2 consumption in rat portal vein. Am J Physiol. 1983 Mar;244(3):C250–C258. doi: 10.1152/ajpcell.1983.244.3.C250. [DOI] [PubMed] [Google Scholar]
  15. Himpens B., Matthijs G., Somlyo A. V., Butler T. M., Somlyo A. P. Cytoplasmic free calcium, myosin light chain phosphorylation, and force in phasic and tonic smooth muscle. J Gen Physiol. 1988 Dec;92(6):713–729. doi: 10.1085/jgp.92.6.713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Iino M. Tension responses of chemically skinned fibre bundles of the guinea-pig taenia caeci under varied ionic environments. J Physiol. 1981 Nov;320:449–467. doi: 10.1113/jphysiol.1981.sp013961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Khromov A. S., Somlyo A. V., Somlyo A. P. Nucleotide binding by actomyosin as a determinant of relaxation kinetics of rabbit phasic and tonic smooth muscle. J Physiol. 1996 May 1;492(Pt 3):669–673. doi: 10.1113/jphysiol.1996.sp021336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Khromov A., Somlyo A. V., Trentham D. R., Zimmermann B., Somlyo A. P. The role of MgADP in force maintenance by dephosphorylated cross-bridges in smooth muscle: a flash photolysis study. Biophys J. 1995 Dec;69(6):2611–2622. doi: 10.1016/S0006-3495(95)80132-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kitazawa T., Gaylinn B. D., Denney G. H., Somlyo A. P. G-protein-mediated Ca2+ sensitization of smooth muscle contraction through myosin light chain phosphorylation. J Biol Chem. 1991 Jan 25;266(3):1708–1715. [PubMed] [Google Scholar]
  20. Krisanda J. M., Paul R. J. Phosphagen and metabolite content during contraction in porcine carotid artery. Am J Physiol. 1983 May;244(5):C385–C390. doi: 10.1152/ajpcell.1983.244.5.C385. [DOI] [PubMed] [Google Scholar]
  21. Martin H., Barsotti R. J. Relaxation from rigor of skinned trabeculae of the guinea pig induced by laser photolysis of caged ATP. Biophys J. 1994 Apr;66(4):1115–1128. doi: 10.1016/S0006-3495(94)80892-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Moreland R. S., Murphy R. A. Determinants of Ca2+-dependent stress maintenance in skinned swine carotid media. Am J Physiol. 1986 Dec;251(6 Pt 1):C892–C903. doi: 10.1152/ajpcell.1986.251.6.C892. [DOI] [PubMed] [Google Scholar]
  23. Murphy R. A. What is special about smooth muscle? The significance of covalent crossbridge regulation. FASEB J. 1994 Mar 1;8(3):311–318. doi: 10.1096/fasebj.8.3.8143937. [DOI] [PubMed] [Google Scholar]
  24. Nishiye E., Somlyo A. V., Török K., Somlyo A. P. The effects of MgADP on cross-bridge kinetics: a laser flash photolysis study of guinea-pig smooth muscle. J Physiol. 1993 Jan;460:247–271. doi: 10.1113/jphysiol.1993.sp019470. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. SERAYDARIAN K., MOMMAERTS W. F., WALLNER A. The amount and compartmentalization of adenosine diphosphate in muscle. Biochim Biophys Acta. 1962 Dec 17;65:443–460. doi: 10.1016/0006-3002(62)90447-x. [DOI] [PubMed] [Google Scholar]
  26. Somlyo A. P. Myosin isoforms in smooth muscle: how may they affect function and structure? J Muscle Res Cell Motil. 1993 Dec;14(6):557–563. doi: 10.1007/BF00141552. [DOI] [PubMed] [Google Scholar]
  27. Somlyo A. P., Somlyo A. V. Signal transduction and regulation in smooth muscle. Nature. 1994 Nov 17;372(6503):231–236. doi: 10.1038/372231a0. [DOI] [PubMed] [Google Scholar]
  28. Somlyo A. V., Goldman Y. E., Fujimori T., Bond M., Trentham D. R., Somlyo A. P. Cross-bridge kinetics, cooperativity, and negatively strained cross-bridges in vertebrate smooth muscle. A laser-flash photolysis study. J Gen Physiol. 1988 Feb;91(2):165–192. doi: 10.1085/jgp.91.2.165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Tashiro M., Konishi M. Basal intracellular free Mg2+ concentration in smooth muscle cells of guinea pig tenia cecum: intracellular calibration of the fluorescent indicator furaptra. Biophys J. 1997 Dec;73(6):3358–3370. doi: 10.1016/S0006-3495(97)78360-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Trinkle-Mulcahy L., Siegman M. J., Butler T. M. Metabolic characteristics of alpha-toxin-permeabilized smooth muscle. Am J Physiol. 1994 Jun;266(6 Pt 1):C1673–C1683. doi: 10.1152/ajpcell.1994.266.6.C1673. [DOI] [PubMed] [Google Scholar]
  31. Vyas T. B., Mooers S. U., Narayan S. R., Siegman M. J., Butler T. M. Cross-bridge cycling at rest and during activation. Turnover of myosin-bound ADP in permeabilized smooth muscle. J Biol Chem. 1994 Mar 11;269(10):7316–7322. [PubMed] [Google Scholar]
  32. Vyas T. B., Mooers S. U., Narayan S. R., Witherell J. C., Siegman M. J., Butler T. M. Cooperative activation of myosin by light chain phosphorylation in permeabilized smooth muscle. Am J Physiol. 1992 Jul;263(1 Pt 1):C210–C219. doi: 10.1152/ajpcell.1992.263.1.C210. [DOI] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES