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Acta Physiologica 2010; Volume 200, Supplement 681
Abstracts of the 61st National Congress of the Italian Physiological Society
9/15/2010-9/17/2010
Varese, Italy
FUNCTIONAL CHARACTERIZATION OF SATELLITE CELLS DERIVED FROM MLC/MIGF1 TRANSGENIC MICE SKELETAL MUSCLE
Abstract number: P89
MARIGGIO1,3 MA, GUARNIERI1,3 S, MORABITO1,3 C, BARBERI2,3 L, MUSARO2,3 A, FANO1,3 G
1Dept Neuroscience and Imaging, and CeSI, Univ. of G.dAnnunzio of Chieti-Pescara, Chieti
2Dept Histology and Medical Embryology, Univ. of Rome La Sapeinza, Roma
3IIM, Italy
Introduction
In MLC/mIGF1 transgenic model, IGF1 gene is regulated by the promoter of myosin light chain (MLC) which only in fast fibres produces autocrine IGF1. From the 5th week after birth, these animals show muscle hypertrophy and consequent increased muscle strength in respect to wild type. It is well known that the muscle reparative/regenerative machinery derives from the recruitment of satellite cell pool, strongly influenced by gene activation and environment conditions. The aim of this work is to verify if the overexpression of IGF1 is able to modify some functional features of satellite cells during the differrentiative process. In particular, we focused our attention on the analyses of parameters directly involved in excitation-contraction cycle (Ca2+ handling and sarcolemmal electrical properties).
Methods
Videoimaging on single cells was used to monitor intracellular calcium variations, and patch clamp technique in whole cell configuration to assay membrane electric properties.
Results
The results showed an increased functional DHPR-binding and increased outward potassium currents in satellite cells derived from MLC/mIGF1 mice in respect to those from wild type animals. Transgenic satellite cells appeared differently sensitive to ATP and ACh stimuli, both physiological regulatory factors of muscle activity.
In conclusion, these preliminary data showed that a higher mIGF1 level could directly influence the fibre capacity to activate the contractile apparatus.
To cite this abstract, please use the following information:
Acta Physiologica 2010; Volume 200, Supplement 681 :P89