Summary

Primary Culture of Adult Rat Heart Myocytes

Published: June 16, 2009
doi:

Summary

In this paper, we described a typical way to isolate and culture adult rat heart myocytes. Collagenase and protease are used to digest and isolate single myocytes. Myocytes cultured follow this protocol meet most experiment requirements.

Abstract

Cultured primary adult rodent heart cells are an important model system for cardiovascular research. Nevertheless, establishment of robust, viable cultured adult myocytes can be a technically challenging, rate-limiting step for many researchers. Here we described a protocol to obtain a high yield of adult rat heart myocytes that remain viable in culture for several days. The heart is isolated and perfused with collagenase and protease under low Ca2+ conditions to recover single myocytes. Ca2+-tolerant cells are obtained by stepwise increases in extracellular Ca2+ concentration in three subsequent wash steps. Cells are filtered, resuspended in culture medium, and plated on laminin coated slips. Cultured myocytes obtained using this protocol are viable for up to four days and are suitable for most experiments including electrophysiology, biochemistry, imaging and molecular biology.

Protocol

Part I. Preparation for surgery The day before the rat surgery, make certain that all solutions are made, but do not add any enzymes yet. Buffers A, B and the wash buffer should all be filtered for sterility prior to storage. The buffers should all be stored at 4 °C. 6-well tissue culture plates must be plated with 10-20 μg/mL laminin in 2 mL 1XSFM the day before as well, and should be stored at 37 °C in a CO2 incubator. On the day of the surgery, prepare the surgical i…

Discussion

A critical step is the speed with which the isolated heart is hung up on the perfusion system. The length of the enzymatic digestion period may be a little different for each rat. The adjustment depends on how soft the heart becomes after the regular period of digestion. The slowly recovery of Ca2+ after enzyme digestion is essential for obtaining Ca2+-tolerant healthy cells.

For guinea pig, the protocol is the same except hyaluronidase is used instead of Protease XIV. …

Materials

Material Name Tipo Company Catalogue Number Comment
NaCl   Sigma S6191  
KCl   Sigma P9541  
HEPES   Sigma H4034  
K2HPO4   Sigma P9666  
MgSO4   Fluka 63068  
Glucose   Sigma G7021  
CaCl2   Sigma C7902  
Heparin Sodium Salt   Sigma H4784  
Collagenase Type II   Worthington Biochemical LS004176  
Protease XIV   Sigma P5147  
2,3-Butanedione Monoxime (BDM)   Sigma B0753  
Carnitine   Sigma C9500  
Taurine   Sigma T0625  
Glutamic Acid   Sigma G1501  
BSA   Sigma A3294  
Creatine   Sigma C3630  
Antibiotic   Cellgro 30-009-CI  
Media 199   GIBCO 11150  
FBS   Hyclone SH30071.03  
Laminin   BD Bioscience 354232  
water bath   Fisher Scientific 15-462-5  
variable flow chemical pump   Fisher Scientific 15-077-67  
6-well culture plate   Corning 3516  

Referências

  1. Miriyala, J., Nguyen, T., Yue, D. T., Colecraft, H. M. Role of CaVbeta subunits, and lack of functional reserve, in protein kinase A modulation of cardiac CaV1.2 channels. Circ Res. 102 (7), e54-e64 (2008).
  2. SX, T. a. k. a. h. a. s. h. i., Mittman, S., Colecraft, H. M. Distinctive modulatory effects of five human auxiliary beta2 subunit splice variants on L-type calcium channel gating. Biophys. , 84-845 (2003).
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Xu, X., Colecraft, H. M. Primary Culture of Adult Rat Heart Myocytes. J. Vis. Exp. (28), e1308, doi:10.3791/1308 (2009).

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