Literature DB >> 14500766

Free magnesium concentration in salamander photoreceptor outer segments.

Chunhe Chen1, Kei Nakatani, Yiannis Koutalos.   

Abstract

Magnesium ions (Mg2+) play an important role in biochemical functions. In vertebrate photoreceptor outer segments, numerous reactions utilize MgGTP and MgATP, and Mg2+ also regulates several of the phototransduction enzymes. Although Mg2+ can pass through light-sensitive channels under certain conditions, no clear extrusion mechanism has been identified and removing extracellular Mg2+ has no significant effect on the light sensitivity or the kinetics of the photoresponse. We have used the fluorescent Mg2+ dye Furaptra to directly measure and monitor the free Mg2+ concentration in photoreceptor outer segments and examine whether the free Mg2+ concentration changes under physiological conditions. Resting free Mg2+ concentrations in bleached salamander rod and cone photoreceptor cell outer segments were 0.86 +/- 0.06 and 0.81 +/- 0.09 mM, respectively. The outer segment free Mg2+ concentration was not significantly affected by changes in extracellular pH, Ca2+ and Na+, excluding a significant role for the respective exchangers in the regulation of Mg2+ homeostasis. The resting free Mg2+ concentration was also not significantly affected by exposure to 0 Mg2+, suggesting the lack of significant basal Mg2+ flux. Opening the cGMP-gated channels led to a significant increase in the Mg2+ concentration in the absence of Na+ and Ca2+, but not in their presence, indicating that depolarization can cause a significant Mg2+ influx only in the absence of other permeant ions, but not under physiological conditions. Finally, light stimulation did not change the Mg2+ concentration in the outer segments of dark-adapted photoreceptors. The results suggest that there are no influx and efflux pathways that can significantly affect the Mg2+ concentration in the outer segment under physiological conditions. Therefore, it is unlikely that Mg2+ plays a significant role in the dynamic modulation of phototransduction.

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Year:  2003        PMID: 14500766      PMCID: PMC2343491          DOI: 10.1113/jphysiol.2003.053280

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  33 in total

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Authors:  Chunhe Chen; Yunhai Jiang; Yiannis Koutalos
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Authors:  W E Robinson; W A Hagins
Journal:  Nature       Date:  1979-08-02       Impact factor: 49.962

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Journal:  J Physiol       Date:  1974-11       Impact factor: 5.182

5.  Elemental distribution in Rana pipiens retinal rods: quantitative electron probe analysis.

Authors:  A P Somlyo; B Walz
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Authors:  M W Kaplan
Journal:  Exp Eye Res       Date:  1985-05       Impact factor: 3.467

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Authors:  P P Schnetkamp
Journal:  Biochemistry       Date:  1981-04-28       Impact factor: 3.162

10.  Light-dependent changes in outer segment free-Ca2+ concentration in salamander cone photoreceptors.

Authors:  A P Sampath; H R Matthews; M C Cornwall; J Bandarchi; G L Fain
Journal:  J Gen Physiol       Date:  1999-02       Impact factor: 4.086

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  22 in total

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Review 3.  Ca(2+)-modulated vision-linked ROS-GC guanylate cyclase transduction machinery.

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5.  Preparation of living isolated vertebrate photoreceptor cells for fluorescence imaging.

Authors:  Nicholas P Boyer; Chunhe Chen; Yiannis Koutalos
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6.  Structural insights into activation of the retinal L-type Ca²⁺ channel (Cav1.4) by Ca²⁺-binding protein 4 (CaBP4).

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7.  Guanylate cyclase-activating protein 2 contributes to phototransduction and light adaptation in mouse cone photoreceptors.

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8.  The R838S Mutation in Retinal Guanylyl Cyclase 1 (RetGC1) Alters Calcium Sensitivity of cGMP Synthesis in the Retina and Causes Blindness in Transgenic Mice.

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9.  Effects of Ca2+, Mg2+, and myristoylation on guanylyl cyclase activating protein 1 structure and stability.

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Review 10.  Mg2+/Ca2+ cation binding cycle of guanylyl cyclase activating proteins (GCAPs): role in regulation of photoreceptor guanylyl cyclase.

Authors:  Alexander M Dizhoor; Elena V Olshevskaya; Igor V Peshenko
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