A data‐driven methodology reveals novel myofiber clusters in older human muscles. Issue 4 (5th March 2020)

• Record Type: Journal Article
• Authors: Raz, Yotam; van den Akker, Erik B.; Roest, Tijmen; Riaz, Muhammad; van de Rest, Ondine; Suchiman, H. Eka D.; Lakenberg, Nico; Stassen, Stefanie A.; van Putten, Maaike; Feskens, Edith J. M.; Reinders, Marcel J. T.; Goeman, Jelle; Beekman, Marian; Raz, Vered; Slagboom, Pieternella Eline
• Is Part Of: FASEB journal. Volume 34:Issue 4(2020)
• Page Start: 5525
• Page End: 5537
• Publication Date: 2020-03-05
• Subjects: bioinformatics -- clustering -- fibertyping -- human -- muscle -- muscle health -- myofiber -- myosin heavy chain -- RNA-sequencing -- sarcomere; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201902350R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract: Skeletal muscles control posture, mobility and strength, and influence whole‐body metabolism. Muscles are built of different types of myofibers, each having specific metabolic, molecular, and contractile properties. Fiber classification is, therefore, regarded the key for understanding muscle biology, (patho‐) physiology. The expression of three myosin heavy chain (MyHC) isoforms, MyHC‐1, MyHC‐2A, and MyHC‐2X, marks myofibers in humans. Typically, myofiber classification is performed by an eye‐based histological analysis. This classical approach is insufficient to capture complex fiber classes, expressing more than one MyHC‐isoform. We, therefore, developed a methodological procedure for high‐throughput characterization of myofibers on the basis of multiple isoforms. The mean fluorescence intensity of the three most abundant MyHC isoforms was measured per myofiber in muscle biopsies of 56 healthy elderly adults, and myofiber classes were identified using computational biology tools. Unsupervised clustering revealed the existence of six distinct myofiber clusters. A comparison with the visual assessment of myofibers using the same images showed that some of these myofiber clusters could not be detected or were frequently misclassified. The presence of these six clusters was reinforced by RNA expressions levels of sarcomeric genes. In addition, one of the clusters, expressing all three MyHC isoforms, correlated with histological measures of muscle health. To conclude, this methodological procedure enables deep characterization of the complex muscle heterogeneity. This study opens opportunities to further investigate myofiber composition in comparative studies.