Battey Edmund, Dos Santos Matthieu, Biswas Dipsikha, Maire Pascal, Sakamoto Kei
Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Capital Region, Denmark; Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Capital Region, Denmark.
Department of Molecular Biology, the Hamon Center for Regenerative Science and Medicine, and Senator Paul D. Wellstone Muscular Dystrophy Specialized Research Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
STAR Protoc. 2024 Dec 20;5(4):103424. doi: 10.1016/j.xpro.2024.103424. Epub 2024 Nov 1.
We outline a protocol to visualize all mouse lower hindlimb skeletal muscles simultaneously. We describe procedures for orientating the whole lower hindlimb in gum tragacanth prior to freezing, simplifying the proceeding experimental steps, and enhancing the comprehensiveness of characterizations. We then detail steps for quantifying muscle fiber size and fiber type characteristics in a single cryosection using histochemistry and immunofluorescence. This protocol can be applied to histological and (immuno)histochemical evaluations such as muscle regeneration, fibrosis, enzymatic activity, and glycogen content.
我们概述了一种同时可视化所有小鼠后肢下部骨骼肌的方案。我们描述了在冷冻前将整个后肢下部在黄蓍胶中定向的程序,简化了后续的实验步骤,并提高了表征的全面性。然后,我们详细介绍了使用组织化学和免疫荧光在单个冷冻切片中量化肌纤维大小和纤维类型特征的步骤。该方案可应用于组织学和(免疫)组织化学评估,如肌肉再生、纤维化、酶活性和糖原含量。