Optical control of calcium-regulated exocytosis

Mercè Izquierdo-Serra, Dirk Trauner, Artur Llobet, Pau Gorostiza

Research output: Contribution to journalArticle

Abstract

Background Neurons signal to each other and to non-neuronal cells as those in muscle or glands, by means of the secretion of neurotransmitters at chemical synapses. In order to dissect the molecular mechanisms of neurotransmission, new methods for directly and reversibly triggering neurosecretion at the presynaptic terminal are necessary. Here we exploit the calcium permeability of the light-gated channel LiGluR in order to reversibly manipulate cytosolic calcium concentration, thus controlling calcium-regulated exocytosis. Methods Bovine chromaffin cells expressing LiGluR were stimulated with light. Exocytic events were detected by amperometry or by whole-cell patch-clamp to quantify membrane capacitance and calcium influx. Results Amperometry reveals that optical stimulation consistently triggers exocytosis in chromaffin cells. Secretion of catecholamines can be adjusted between zero and several Hz by changing the wavelength of illumination. Differences in secretion efficacy are found between the activation of LiGluR and native voltage-gated calcium channels (VGCCs). Our results show that the distance between sites of calcium influx and vesicles ready to be released is longer when calcium influx is triggered by LiGluR instead of native VGCCs. Conclusion LiGluR activation directly and reversibly increases the intracellular calcium concentration. Light-gated calcium influx allows for the first time to control calcium-regulated exocytosis without the need of applying depolarizing solutions or voltage clamping in chromaffin cells. General significance LiGluR is a useful tool to study the secretory mechanisms and their spatiotemporal patterns in neurotransmission, and opens a window to study other calcium-dependent processes such as muscular contraction or cell migration.

Original languageEnglish (US)
Pages (from-to)2853-2860
Number of pages8
JournalBiochimica et Biophysica Acta - General Subjects
Volume1830
Issue number3
DOIs
StatePublished - Mar 2013

Fingerprint

Exocytosis
Calcium
Chromaffin Cells
Calcium Channels
Light
Synaptic Transmission
Electric potential
Chemical activation
Neurosecretion
Presynaptic Terminals
Clamping devices
Muscle Contraction
Lighting
Constriction
Synapses
Neurons
Catecholamines
Cell Movement
Neurotransmitter Agents
Muscle

Keywords

  • Calcium
  • Exocytosis
  • Light-gated glutamate receptor (LiGluR)
  • Neurotransmission
  • Optical control
  • Optogenetics

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology

Cite this

Izquierdo-Serra, M., Trauner, D., Llobet, A., & Gorostiza, P. (2013). Optical control of calcium-regulated exocytosis. Biochimica et Biophysica Acta - General Subjects, 1830(3), 2853-2860. https://doi.org/10.1016/j.bbagen.2012.11.003

Optical control of calcium-regulated exocytosis. / Izquierdo-Serra, Mercè; Trauner, Dirk; Llobet, Artur; Gorostiza, Pau.

In: Biochimica et Biophysica Acta - General Subjects, Vol. 1830, No. 3, 03.2013, p. 2853-2860.

Research output: Contribution to journalArticle

Izquierdo-Serra, M, Trauner, D, Llobet, A & Gorostiza, P 2013, 'Optical control of calcium-regulated exocytosis', Biochimica et Biophysica Acta - General Subjects, vol. 1830, no. 3, pp. 2853-2860. https://doi.org/10.1016/j.bbagen.2012.11.003
Izquierdo-Serra, Mercè ; Trauner, Dirk ; Llobet, Artur ; Gorostiza, Pau. / Optical control of calcium-regulated exocytosis. In: Biochimica et Biophysica Acta - General Subjects. 2013 ; Vol. 1830, No. 3. pp. 2853-2860.
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