Optical Microscopy and the Extracellular Matrix Structure: A Review

• Published in: Cells (Basel, Switzerland) Vol. 10; no. 7; p. 1760
• Main Authors: Poole, Joshua J A, Mostaço-Guidolin, Leila B
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 12.07.2021; MDPI
• Subjects: Animals; Cancer; Chronic Disease; Collagen; Confocal microscopy; ECM; elastin; Extracellular matrix; Extracellular Matrix - metabolism; Fibroblasts; Fluorescence; Growth factors; Homeostasis; Humans; Hyaluronic acid; imaging; Light; Light microscopy; Localization; Macromolecules; Mechanical properties; Microenvironments; Microscopy; Microscopy, Fluorescence; Optical Imaging; optics; Organ Specificity; Proteins; Review; Reviews; Structure-function relationships; Visualization; proteoglycans; fibers; fibronectin; collagen; microscopy; super resolution; optics; elastin; imaging; ECM
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells10071760

Biological tissues are not uniquely composed of cells. A substantial part of their volume is extracellular space, which is primarily filled by an intricate network of macromolecules constituting the extracellular matrix (ECM). The ECM serves as the scaffolding for tissues and organs throughout the body, playing an essential role in their structural and functional integrity. Understanding the intimate interaction between the cells and their structural microenvironment is central to our understanding of the factors driving the formation of normal versus remodelled tissue, including the processes involved in chronic fibrotic diseases. The visualization of the ECM is a key factor to track such changes successfully. This review is focused on presenting several optical imaging microscopy modalities used to characterize different ECM components. In this review, we describe and provide examples of applications of a vast gamut of microscopy techniques, such as widefield fluorescence, total internal reflection fluorescence, laser scanning confocal microscopy, multipoint/slit confocal microscopy, two-photon excited fluorescence (TPEF), second and third harmonic generation (SHG, THG), coherent anti-Stokes Raman scattering (CARS), fluorescence lifetime imaging microscopy (FLIM), structured illumination microscopy (SIM), stimulated emission depletion microscopy (STED), ground-state depletion microscopy (GSD), and photoactivated localization microscopy (PALM/fPALM), as well as their main advantages, limitations.