Optical Microscopy and Electron Microscopy for the Morphological Evaluation of Tendons: A Mini Review.
Ming-You XuJie LiuJiayi SunXinrong XuYongcheng HuBin LiuPublished in: Orthopaedic surgery (2020)
The morphological characteristics of tendons have been thoroughly evaluated via microscopy. Optical microscopy and electron microscopy are the most commonly used techniques for tendon tissue observation. According to the principles of both microscopy types, preparation and evaluation methods vary. Simple optical microscopy is commonly used in the observation of cells and extracellular matrix, and many stains, including hematoxylin-eosin, Van Gieson, Prussian blue, Alcian blue, and toluidine blue, are used for evaluating cells, collagen fiber arrangement, and noncollagenous proteins. Histological scoring systems have been used in many studies for semi-quantification. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) are the most commonly used electron microscopy types, and special consideration is needed for the fixation and embedding protocols. Glutaraldehyde followed by osmium is most commonly used in the chemical fixation of tendon tissue, followed by epoxy resin embedment. Longitudinal sections captured in SEM images show the arrangement of collagen fibrils and the cells and lipid drops among them, while cross sections captured in TEM images show the diameter and distribution of collagen fibrils. SEM and TEM are used together for comprehensive evaluations. This mini review is focused on the preparation methodology and related evaluation indexes for the morphological evaluation of tendons.
Keyphrases
- electron microscopy
- high resolution
- high speed
- induced apoptosis
- optical coherence tomography
- single molecule
- cell cycle arrest
- extracellular matrix
- high throughput
- label free
- deep learning
- minimally invasive
- endoplasmic reticulum stress
- convolutional neural network
- signaling pathway
- cross sectional
- machine learning
- mass spectrometry
- pi k akt
- single cell
- drug induced
- tandem mass spectrometry