Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The intracellular Na+ concentration ([Na+]i) in cardiac myocytes is altered during cardiac diseases. [Na+]i is an important regulator of intracellular Ca2+. We introduce a novel approach to measure [Na+]i in freshly isolated murine atrial myocytes using an electron multiplying charged coupled device (EMCCD) camera and a rapid, controllable illuminator.

Abstract

Intracellular sodium concentration ([Na+]i) is an important regulator of intracellular Ca2+. Its study provides insight into the activation of the sarcolemmal Na+/Ca2+ exchanger, the behavior of voltage-gated Na+ channels and the Na+,K+-ATPase. Intracellular Ca2+ signaling is altered in atrial diseases such as atrial fibrillation. While many of the mechanisms underlying altered intracellular Ca2+ homeostasis are characterized, the role of [Na+]i and its dysregulation in atrial pathologies is poorly understood. [Na+]i in atrial myocytes increases in response to increasing stimulation rates. Responsiveness to external field stimulation is therefore crucial for [Na+]i measurements in these cells. In addition, the long preparation (dye-loading) and experiment duration (calibration) require an isolation protocol that yields atrial myocytes of exceptional quality. Due to the small size of mouse atria and the composition of the intercellular matrix, the isolation of high quality adult murine atrial myocytes is difficult. Here, we describe an optimized Langendorff-perfusion based isolation protocol that consistently delivers a high yield of high quality atrial murine myocytes.

Sodium-binding benzofuran isophthalate (SBFI) is the most commonly used fluorescent Na+ indicator. SBFI can be loaded into the cardiac myocyte either in its salt form through a glass pipette or as an acetoxymethyl (AM) ester that can penetrate the myocyte’s sarcolemmal membrane. Intracellularly, SBFI-AM is de-esterified by cytosolic esterases. Due to variabilities in membrane penetration and cytosolic de-esterification each cell has to be calibrated in situ. Typically, measurements of [Na+]i using SBFI whole-cell epifluorescence are performed using a photomultiplier tube (PMT). This experimental set-up allows for only one cell to be measured at one time. Due to the length of myocyte dye loading and the calibration following each experiment data yield is low. We therefore developed an EMCCD camera-based technique to measure [Na+]i. This approach permits simultaneous [Na+]i measurements in multiple myocytes thus significantly increasing experimental yield.

Introduction

In atrial diseases (e.g., atrial fibrillation [AF]) intracellular Ca2+ signaling is profoundly altered1. While many of the underlying mechanisms of ‘remodeled’ intracellular Ca2+ signaling in AF have been well characterized2,3, the role an altered intracellular sodium concentration ([Na+]i) may play is poorly understood. [Na+]i is an important regulator of intracellular Ca2+. The study of [Na+]i can provide insight into the activation of the sarcolemmal Na+/Ca2+....

Protocol

All methods described here have been approved by the Institutional Animal Care and Use Committee (IACUC) of the University of Maryland, Baltimore.

1. Isolation of atrial myocytes from adult murine hearts

  1. Place each mouse in a precision vaporizer and induction chamber gassed with isoflurane in 100% oxygen.
  2. Set the isoflurane flow to 1% until the animal is unresponsive before giving an intraperitoneal (IP) heparin injection (1–1.25 U/g) 15 min before euthanasia.
  3. .......

Representative Results

Evaluation of Atrial Cell Quality
Freshly isolated atrial myocytes were evaluated based on cell morphology and responsiveness to field stimulation as outlined in the protocol in six consecutive atrial cell isolations. Data shown in Figure 2 show a very high percentage of rod-shaped atrial myocytes that retain clear cross striation. Similarly, about 50% of atrial cells respond to high rates of external field stimulation up to 3 Hz.

<.......

Discussion

Here we introduce a novel EMCCD camera-based technique for the simultaneous quantitative measurement of [Na+]i in multiple viable atrial myocytes using sodium-binding benzofuran isophthalate (SBFI). The approach described here is the first to allow for the simultaneous measurement of [Na+]i in multiple cells. The main advantages this new protocol presenta are (i) the significant increase in experimental yield and (ii) the reduction in illumination intensity and duration due to .......

Acknowledgements

This work was supported by a Scientist Development Grant from the American Heart Association (14SDG20110054) to MG; the NIH Interdisciplinary Training Grant in Muscle Biology (T32 AR007592) and the NIH Cardiovascular Disease Training Grant (2T32HL007698-22A1) to LG; a Scientist Development Grant from the American Heart Association (15SDG22100002) to LB and by NIH grants R01 HL106056, R01 HL105239 and U01 HL116321 to WJL.

....

Materials

NameCompanyCatalog NumberComments
2,3-Butanedione monoxime (BDM)Sigma-AldrichB0753
340 Excitation FilterChromaET40X25 mm
380 Excitation FilterChromaET80X25 mm
510 Emission FilterChromaET510/80m25 mm
Bovine Serum Albumin (BSA)Sigma-AldrichA7906
Bubble trapBD Medical Technologies904477Custom made from a 5 ml Luer Lok Syringe, which is located in the tubing path from the perfusing solution to the cannula
CaCl2 solutionSigma-Aldrich21115
CannulaBD Medical Technologies305167Custom made from a 22 G x 1 1/2 inch needle. Cut to 1 inch and sand 1mm distal tip.
Cell ChamberCustom machined with an opening that can securely hold a 25 mm glass cover slip and with a cover that has an inlet and an outlet port for perfusion.
Circulating Water BathVWR
Collagenase IIWorthingtonLS004176Specific activity 290 U/g
CreatinineSigma-AldrichC0780
DG5-plus illuminatorSutter InstrumentLambda DG-4/DG-5 Plus
DMSOThermo FischerBP231
EGTASigma-AldrichE4378
EMCCD cameraPrinceton InstrumentsProEM-HS
Fine HemostatsFine Science Tools130-20
Fine ScissorsFine Science Tools14060-10
Forceps SupergripFine Science Tools00632-11
Glass Cover slipsVWR483808925 mm circle
GlucoseSigma-AldrichG7528
Gramicidin DSigma-AldrichG5002
HEPESSigma-AldrichH3375
Inner silicon TubingVWRVWRselect brand silicon tubing
Inverted microscopeNikon InstrumentsNikonTE 2000 U
Isolation Tools
K GluconateSigma-AldrichP1847
KCISigma-AldrichP5405
KH2PO4Calbiochem529568
Langendorff perfusion apparatus
MgCl2.6H2O *Sigma-AldrichM0250
MyoPacer Cell StimulatorIonOptix
Na GluconateSigma-AldrichS2054
NaClSigma-AldrichS9888
NaH2PO4Sigma-AldrichS9390
Natural Mouse LamininThermo Fischer230170150.5-2.0 mg/ml
Outer tubingVWR
Petri dish 35X10 mmFalcon351008
PowerLoadThermo FischerP10020
Protease XXIVSigma-AldrichP8038
SBFI-AMThermo FischerS1264
Silk sutureFine Science Tools18020-500.12 mm diameter
Small Spring scissorsFine Science Tools15000-03
Standard Pattern ForcepsFine Science Tools11000-12
StrophanthidinSigma-AldrichG5884
Surgical Scissors Tough CutFine Science Tools14054-13
Suture Tying ForcepsFine Science Tools00272-13
TaurineSigma-AldrichT0625
TrisbaseSigma-AldrichTRIS-RO
TrypsinSigma-AldrichT0303
UVFS Reflective 0.1 ND FilterThorlabsNDUV01B25 mm
UVFS Reflective 0.2 ND FilterThorlabsNDUV02B25 mm
UVFS Reflective 0.3 ND FilterThorlabsNDUV03B25 mm
UVFS Reflective 0.5 ND FilterThorlabsNDUV05B25 mm
UVFS Reflective 1 ND FilterThorlabsNDUV010B25 mm

References

  1. Greiser, M., et al. Tachycardia-induced silencing of subcellular Ca2+ signaling in atrial myocytes. Journal of Clinical Investigation. , (2014).
  2. Greiser, M., Lederer, W. J., Schotten, U. Alterati....

Explore More Articles

Intracellular Sodium ConcentrationNa iAtrial MyocytesNa Ca2 ExchangerVoltage gated Na ChannelsNaK ATPaseIntracellular Ca2 SignalingAtrial FibrillationLangendorff perfusionSBFISodium binding Benzofuran IsophthalateFluorescent Na IndicatorEMCCD Camera

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2024 MyJoVE Corporation. All rights reserved