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Mouse lemur, a new animal model to investigate cardiac pacemaker activity in primates

Authors :
Mattia L. DiFrancesco
Romain Davaze
Eleonora Torre
Pietro Mesirca
Manon Marrot
Corinne Lautier
Pascaline Fontes
Joёl Cuoq
Anne Fernandez
Ned Lamb
Fabien Pifferi
Nadine Mestre-Francés
Matteo E. Mangoni
Angelo G. Torrente
Publication Year :
2021
Publisher :
Cold Spring Harbor Laboratory, 2021.

Abstract

BackgroundGray mouse lemurs (Microcebus murinus) are the smallest and most ancestral primates known. Their size falls in between that of mice and rats, and their genetic proximity to humans makes them an emerging model to study age-related neurodegeneration. Since mouse lemurs replicate similar senescence processes of humans, they constitute a useful model for studying cardiovascular dysfunctions. However, their cardiac physiology is unknown. Thus, we investigated the cardiac pacemaker activity generated by the sinoatrial node (SAN) of mouse lemurs, presenting the first characterization of heart automaticity in nonhuman primates.Methods and ResultsWe recorded cardiac automaticity in mouse lemurs and in their SAN tissues and pacemaker myocytes. Mouse lemurs have a heart rate (HR) in between those of mice and rats and a similar generation of the SAN electrical impulse. Their SAN myocytes express the main pacemaker currents at densities similar to mice: the hyperpolarization-activated current (If) and the L-type (Ica,L) and T-type (Ica,T) calcium currents. Conversely, their ventricular depolarization resembles that of large mammals and despite the small size of mouse lemurs, the total number of heartbeats in their life corresponds to what can be attained by humans.Using muscle-derived stem cells (MDSCs) from mouse lemurs, we also differentiated pacemaker-like (PML) cells showing spontaneous automaticity and expressing markers of native SAN myocytes (HCN4 and connexin-45).ConclusionsOur characterization of heart automaticity in Microcebus murinus provides new opportunities for comparative cardio-physiology studies in primates and with humans and for testing molecules that could modulate age-related dysfunctions of heart rate.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........51ab53372d1ca51a51d7c9acf41baeb3
Full Text :
https://doi.org/10.1101/2021.10.25.465774