Literature DB >> 23092999

Preparation of Drosophila central neurons for in situ patch clamping.

Stefanie Ryglewski1, Carsten Duch.   

Abstract

Short generation times and facile genetic techniques make the fruit fly Drosophila melanogaster an excellent genetic model in fundamental neuroscience research. Ion channels are the basis of all behavior since they mediate neuronal excitability. The first voltage gated ion channel cloned was the Drosophila voltage gated potassium channel Shaker(1,2). Toward understanding the role of ion channels and membrane excitability for nervous system function it is useful to combine powerful genetic tools available in Drosophila with in situ patch clamp recordings. For many years such recordings have been hampered by the small size of the Drosophila CNS. Furthermore, a robust sheath made of glia and collagen constituted obstacles for patch pipette access to central neurons. Removal of this sheath is a necessary precondition for patch clamp recordings from any neuron in the adult Drosophila CNS. In recent years scientists have been able to conduct in situ patch clamp recordings from neurons in the adult brain(3,4) and ventral nerve cord of embryonic(5,6), larval(7,8,9,10), and adult Drosophila(11,12,13,14). A stable giga-seal is the main precondition for a good patch and depends on clean contact of the patch pipette with the cell membrane to avoid leak currents. Therefore, for whole cell in situ patch clamp recordings from adult Drosophila neurons must be cleaned thoroughly. In the first step, the ganglionic sheath has to be treated enzymatically and mechanically removed to make the target cells accessible. In the second step, the cell membrane has to be polished so that no layer of glia, collagen or other material may disturb giga-seal formation. This article describes how to prepare an identified central neuron in the Drosophila ventral nerve cord, the flight motoneuron 5 (MN5(15)), for somatic whole cell patch clamp recordings. Identification and visibility of the neuron is achieved by targeted expression of GFP in MN5. We do not aim to explain the patch clamp technique itself.

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Year:  2012        PMID: 23092999      PMCID: PMC3490319          DOI: 10.3791/4264

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  15 in total

1.  Electrophysiological and morphological characterization of identified motor neurons in the Drosophila third instar larva central nervous system.

Authors:  James C Choi; Demian Park; Leslie C Griffith
Journal:  J Neurophysiol       Date:  2003-12-24       Impact factor: 2.714

2.  Characterization of voltage-dependent Ca2+ currents in identified Drosophila motoneurons in situ.

Authors:  Jason W Worrell; Richard B Levine
Journal:  J Neurophysiol       Date:  2008-06-11       Impact factor: 2.714

3.  Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene from Drosophila.

Authors:  D M Papazian; T L Schwarz; B L Tempel; Y N Jan; L Y Jan
Journal:  Science       Date:  1987-08-14       Impact factor: 47.728

4.  Sequence of a probable potassium channel component encoded at Shaker locus of Drosophila.

Authors:  B L Tempel; D M Papazian; T L Schwarz; Y N Jan; L Y Jan
Journal:  Science       Date:  1987-08-14       Impact factor: 47.728

5.  Segmental differences in firing properties and potassium currents in Drosophila larval motoneurons.

Authors:  Subhashini Srinivasan; Kimberley Lance; Richard B Levine
Journal:  J Neurophysiol       Date:  2011-12-07       Impact factor: 2.714

6.  Electrophysiological development of central neurons in the Drosophila embryo.

Authors:  R A Baines; M Bate
Journal:  J Neurosci       Date:  1998-06-15       Impact factor: 6.167

7.  Shaker and Shal mediate transient calcium-independent potassium current in a Drosophila flight motoneuron.

Authors:  Stefanie Ryglewski; Carsten Duch
Journal:  J Neurophysiol       Date:  2009-10-14       Impact factor: 2.714

8.  Morphological identification of the motor neurons innervating the dorsal longitudinal flight muscle of Drosophila melanogaster.

Authors:  K Ikeda; J H Koenig
Journal:  J Comp Neurol       Date:  1988-07-15       Impact factor: 3.215

9.  Spike integration and cellular memory in a rhythmic network from Na+/K+ pump current dynamics.

Authors:  Stefan R Pulver; Leslie C Griffith
Journal:  Nat Neurosci       Date:  2009-12-06       Impact factor: 24.884

10.  The nicotinic acetylcholine receptor Dalpha7 is required for an escape behavior in Drosophila.

Authors:  Amir Fayyazuddin; Mahira A Zaheer; P Robin Hiesinger; Hugo J Bellen
Journal:  PLoS Biol       Date:  2006-02-28       Impact factor: 8.029

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  4 in total

1.  Relating ion channel expression, bifurcation structure, and diverse firing patterns in a model of an identified motor neuron.

Authors:  Marco A Herrera-Valdez; Erin C McKiernan; Sandra D Berger; Stefanie Ryglewski; Carsten Duch; Sharon Crook
Journal:  J Comput Neurosci       Date:  2012-08-11       Impact factor: 1.621

2.  Intra-neuronal Competition for Synaptic Partners Conserves the Amount of Dendritic Building Material.

Authors:  Stefanie Ryglewski; Fernando Vonhoff; Kathryn Scheckel; Carsten Duch
Journal:  Neuron       Date:  2017-01-26       Impact factor: 17.173

3.  Sequential acquisition of cacophony calcium currents, sodium channels and voltage-dependent potassium currents affects spike shape and dendrite growth during postembryonic maturation of an identified Drosophila motoneuron.

Authors:  Stefanie Ryglewski; Lukas Kilo; Carsten Duch
Journal:  Eur J Neurosci       Date:  2014-03-13       Impact factor: 3.386

4.  Different functions of two putative Drosophila α2δ subunits in the same identified motoneurons.

Authors:  Laurin Heinrich; Stefanie Ryglewski
Journal:  Sci Rep       Date:  2020-08-13       Impact factor: 4.379

  4 in total

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