Abstract

Genetic manipulation of signaling proteins is an important tool to study signaling mechanisms. While rabbit sinoatrial node cells (SANC) are an excellent model for the study of autonomic signaling, genetic manipulation of freshly isolated rabbit SANC (f-SANC) is not possible. Here we report important characteristics of a cultured rabbit SANC model (c-SANC) that is suitable for manipulation of gene expression. C-SANC generate regular and rhythmic APs at 34±0.5oC, and beat spontaneously at a lower rate (1.35±0.02Hz, n=803) than f-SANC (2.79±0.04Hz, n=203 p<0.001).

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