Resting myoplasmic free calcium in frog skeletal muscle fibers estimated with fluo-3 - PubMed (original) (raw)
Resting myoplasmic free calcium in frog skeletal muscle fibers estimated with fluo-3
A B Harkins et al. Biophys J. 1993 Aug.
Abstract
Fluo-3 is an unusual tetracarboxylate Ca2+ indicator. For recent lots supplied by Molecular Probes Inc. (Eugene, OR), FMAX, the fluorescence intensity of the indicator in its Ca(2+)-bound form, is approximately 200 times that of FMIN, the fluorescence intensity of the indicator in its Ca(2+)-free form. (For earlier lots, impurities may account for the smaller reported values of FMAX/FMIN, 36-40). We have injected fluo-3 from a high-purity lot into intact single fibers from frog muscle and measured the indicator's absorbance and fluorescence signals at rest (A and F, respectively) and changes in absorbance and fluorescence following action potential stimulation (delta A and delta F signals substantially lagged behind that of the myoplasmic free Ca2+ transient. Our analysis of fluo-3's signals from myoplasm therefore focused on information about the level of resting myoplasmic free [Ca2+] ([Ca2+]r). From A, delta A, and in vitro estimates of fluo-3's molar extinction coefficients, the change in the fraction of fluo-3 in the Ca(2+)-bound form during activity (delta f) was estimated. From delta f, delta F, and F, the fraction of the indicator in the Ca(2+)-bound form in the resting fiber (fr) was estimated by fr = (delta f x F/delta F) + (1-FMAX/FMIN)-1. Since FMAX/FMIN is large, the contribution of the second term to the estimate of fr is small. At 16 degrees C, the mean value (mean +/- S.E.) of fr was 0.086 +/- 0.004 (N = 15). From two estimates of the apparent dissociation constant of fluo-3 for Ca2+ in the myoplasm, 1.09 and 2.57 microM, the average value of [Ca2+]r is calculated to be 0.10 and 0.24 microM, respectively. The smaller of these estimates lies near the upper end of the range of values for [Ca2+]r in frog fibers (0.02-0.12 microM) estimated by others with aequorin and Ca(2+)-selective electrodes. The larger of the estimates lies within the range of values (0.2-0.3 microM) previously estimated in this laboratory with fura red. We conclude that [Ca2+]r in frog fibers is at least 0.1 microM and possibly as large as 0.3 microM.
Comment in
- Ca2+i versus [Ca2+]i.
Morgan KG. Morgan KG. Biophys J. 1993 Aug;65(2):561-2. doi: 10.1016/S0006-3495(93)81087-7. Biophys J. 1993. PMID: 8218883 Free PMC article. No abstract available.
Similar articles
- Use of fura red as an intracellular calcium indicator in frog skeletal muscle fibers.
Kurebayashi N, Harkins AB, Baylor SM. Kurebayashi N, et al. Biophys J. 1993 Jun;64(6):1934-60. doi: 10.1016/S0006-3495(93)81564-9. Biophys J. 1993. PMID: 8369415 Free PMC article. - Myoplasmic calcium transients in intact frog skeletal muscle fibers monitored with the fluorescent indicator furaptra.
Konishi M, Hollingworth S, Harkins AB, Baylor SM. Konishi M, et al. J Gen Physiol. 1991 Feb;97(2):271-301. doi: 10.1085/jgp.97.2.271. J Gen Physiol. 1991. PMID: 2016581 Free PMC article. - Resting cytoplasmic free Ca2+ concentration in frog skeletal muscle measured with fura-2 conjugated to high molecular weight dextran.
Konishi M, Watanabe M. Konishi M, et al. J Gen Physiol. 1995 Dec;106(6):1123-50. doi: 10.1085/jgp.106.6.1123. J Gen Physiol. 1995. PMID: 8786353 Free PMC article. - Kinetic investigations in single muscle fibres using luminescent and fluorescent Ca2+ probes.
Ashley CC, Potter JD, Strang P, Godber J, Walton A, Griffiths PJ. Ashley CC, et al. Cell Calcium. 1985 Apr;6(1-2):159-81. doi: 10.1016/0143-4160(85)90042-9. Cell Calcium. 1985. PMID: 3893726 Review. - Classes and mechanisms of calcium waves.
Jaffe LF. Jaffe LF. Cell Calcium. 1993 Nov;14(10):736-45. doi: 10.1016/0143-4160(93)90099-r. Cell Calcium. 1993. PMID: 8131190 Review.
Cited by
- Cytosolic Ca2+-dependent Ca2+ release activity primarily determines the ER Ca2+ level in cells expressing the CPVT-linked mutant RYR2.
Kurebayashi N, Murayama T, Ota R, Suzuki J, Kanemaru K, Kobayashi T, Ohno S, Horie M, Iino M, Yamashita F, Sakurai T. Kurebayashi N, et al. J Gen Physiol. 2022 Sep 5;154(9):e202112869. doi: 10.1085/jgp.202112869. Epub 2022 Apr 21. J Gen Physiol. 2022. PMID: 35446340 Free PMC article. - Modulation of the intracellular calcium concentration in photoreceptor terminals by a presynaptic metabotropic glutamate receptor.
Koulen P, Kuhn R, Wässle H, Brandstätter JH. Koulen P, et al. Proc Natl Acad Sci U S A. 1999 Aug 17;96(17):9909-14. doi: 10.1073/pnas.96.17.9909. Proc Natl Acad Sci U S A. 1999. PMID: 10449793 Free PMC article. - Fast calcium removal during single twitches in amphibian skeletal muscle fibres.
Caputo C, Bolaños P, Escobar AL. Caputo C, et al. J Muscle Res Cell Motil. 1999 Aug;20(5-6):555-67. doi: 10.1023/a:1005526202747. J Muscle Res Cell Motil. 1999. PMID: 10555074 - Stoichiometry of Na+-Ca2+ exchange is 3:1 in guinea-pig ventricular myocytes.
Hinata M, Yamamura H, Li L, Watanabe Y, Watano T, Imaizumi Y, Kimura J. Hinata M, et al. J Physiol. 2002 Dec 1;545(2):453-61. doi: 10.1113/jphysiol.2002.025866. J Physiol. 2002. PMID: 12456825 Free PMC article. - Ca sparks do not explain all ryanodine receptor-mediated SR Ca leak in mouse ventricular myocytes.
Santiago DJ, Curran JW, Bers DM, Lederer WJ, Stern MD, Ríos E, Shannon TR. Santiago DJ, et al. Biophys J. 2010 May 19;98(10):2111-20. doi: 10.1016/j.bpj.2010.01.042. Biophys J. 2010. PMID: 20483318 Free PMC article.
References
- Biophys J. 1993 Jun;64(6):1934-60 - PubMed
- J Gen Physiol. 1991 Dec;98(6):1141-60 - PubMed
- J Physiol. 1960 Sep;153:386-403 - PubMed
- Science. 1969 Dec 5;166(3910):1297-8 - PubMed
- Proc Natl Acad Sci U S A. 1973 Apr;70(4):982-4 - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous