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Laurens, C.

Publications and source records attributed to Laurens, C..

3 recordsLinked to original sources

MyoFuse: A fully AI-based workflow for automated quantification of skeletal muscle cell fusion in vitro

BackgroundThe myogenic fusion index (FI) is commonly used in skeletal muscle cell culture to assess the ability of myoblasts to form myotubes, as the ratio of myoblast nuclei fused with myotubes over the total number of myoblasts. The manual quantification of the FI from 2D microscopy images is tedious and biased, thus several automated methods have been developed. However, they still face challenges such as efficient nucleus segmentation and classification of fused and isolated myoblast nuclei. Here, we developed a novel workflow entirely based on AI for fully automated and unbiased quantification of the FI. ResultsUsing current methods, we show that myoblast nuclei located above or below myotubes can significantly corrupt accurate FI computation. To circumvent this issue, we developed MyoFuse which enables an accurate and high-throughput segmentation and classification of myonuclei. It comprises a nuclei segmentation step using Cellpose, followed by a classification network trained with Svetlana. MyoFuse demonstrated strong accuracy when tested against manual annotation in mouse C2C12 and human primary myotubes. The trained classifier is able to differentiate myotube nuclei from myoblast nuclei based on myotube cytoplasm staining only. Experimental comparisons also highlighted that the previously developed methods lead to a significant overestimation of the FI. ConclusionIn summary, we underscore the lack of accuracy of traditional methods for automated FI quantification. MyoFuse enables a direct and accurate segmentation of nuclei even in nuclei clusters frequently observed in myotubes. This workflow thus offers a new and more reliable method to evaluate the FI. It also limits the selection bias by processing large images.

cell biology↗

GREM1 is epigenetically reprogrammed in muscle cells after exercise training and controls myogenesis and metabolism

Exercise training improves skeletal muscle function, notably through tissue regeneration by muscle stem cells. Here, we hypothesized that exercise training reprograms the epigenome of muscle cell, which could account for better muscle function. Genome-wide DNA methylation of myotube cultures established from middle-aged obese men before and after endurance exercise training identified a differentially methylated region (DMR) located downstream of Gremlin 1 (GREM1), which was associated with increased GREM1 expression. GREM1 expression was lower in muscle satellite cells from obese, compared to lean mice, and exercise training restored GREM1 levels to those of control animals. We show that GREM1 regulates muscle differentiation through the negative control of satellite cell self-renewal, and that GREM1 controls muscle lineage commitment and lipid oxidation through the AMPK pathway. Our study identifies novel functions of GREM1 and reveals an epigenetic mechanism by which exercise training reprograms muscle stem cells to improve skeletal muscle function.

cell biology↗

Atrial natriuretic peptide orchestrates a coordinated physiological response to fuel non shivering thermogenesis

Atrial natriuretic peptide (ANP) is a cardiac hormone controlling blood volume and arterial pressure in mammals. It is unclear whether and how ANP controls cold-induced thermogenesis in vivo. Here we show that acute cold exposure induces cardiac ANP secretion in mice and humans. Genetic inactivation of ANP promotes cold intolerance and suppresses about half of cold-induced brown adipose tissue (BAT) activation in mice. While white adipocytes are resistant to ANP-mediated lipolysis at thermoneutral temperature in mice, cold exposure renders white adipocytes fully responsive to ANP to activate lipolysis and a thermogenic program, a physiological response which is dramatically suppressed in ANP null mice. ANP deficiency also blunts liver triglycerides and glycogen metabolism thus impairing fuel availability for BAT thermogenesis. ANP directly increases mitochondrial uncoupling and thermogenic genes expression in human white and brown adipocytes. Together, these results indicate that ANP is a major physiological trigger of BAT thermogenesis upon cold exposure in mammals.

physiology↗