1. Gelsolin Contributes to the Motility of A375 Melanoma Cells and This Activity Is Mediated by the Fibrous Extracellular Matrix Protein Profile.
- Author
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Mazurkiewicz E, Makowiecka A, Mrówczyńska E, Kopernyk I, Nowak D, and Mazur AJ
- Subjects
- Basement Membrane pathology, Collagen Type I metabolism, Collagen Type IV metabolism, Extracellular Matrix pathology, Fibronectins metabolism, Gelsolin genetics, Humans, Laminin metabolism, Melanoma genetics, Melanoma pathology, Neoplasm Invasiveness, Podosomes metabolism, Podosomes pathology, Signal Transduction, Skin Neoplasms genetics, Skin Neoplasms pathology, Basement Membrane metabolism, Cell Movement, Extracellular Matrix metabolism, Gelsolin metabolism, Melanoma metabolism, Skin Neoplasms metabolism, Tumor Microenvironment
- Abstract
Skin melanocytes reside on the basement membrane (BM), which is mainly composed of laminin, collagen type IV, and proteoglycans. For melanoma cells, in order to invade into the skin, melanocytes must cross the BM. It has been reported that changes in the composition of the BM accompany melanocytes tumorigenesis. Previously, we reported high gelsolin (GSN)-an actin-binding protein-levels in melanoma cell lines and GSN's importance for migration of A375 cells. Here we investigate whether melanoma cells migrate differently depending on the type of fibrous extracellular matrix protein. We obtained A375 melanoma cells deprived of GSN synthesis and tested their migratory properties on laminin, collagens type I and IV, fibronectin, and Matrigel, which resembles the skin's BM. We applied confocal and structured illuminated microscopy (SIM), gelatin degradation, and diverse motility assays to assess GSN's influence on parameters associated with cells' ability to protrude. We show that GSN is important for melanoma cell migration, predominantly on laminin, which is one of the main components of the skin's BM.
- Published
- 2021
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