Mechanobiological Modulation of In Vitro Astrocyte Reactivity Using Variable Gel Stiffness.

Autor: C Benincasa J; Department of Biochemistry, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo 04039032, Brazil., Madias MI; Department of Bioengineering, University of California San Diego, La Jolla, California 92093, United States., Kandell RM; Department of Bioengineering, University of California San Diego, La Jolla, California 92093, United States., Delgado-Garcia LM; Department of Biochemistry, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo 04039032, Brazil., Engler AJ; Department of Bioengineering, University of California San Diego, La Jolla, California 92093, United States., Kwon EJ; Department of Bioengineering, University of California San Diego, La Jolla, California 92093, United States., Porcionatto MA; Department of Biochemistry, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo 04039032, Brazil.
Jazyk: angličtina
Zdroj: ACS biomaterials science & engineering [ACS Biomater Sci Eng] 2024 Jul 08; Vol. 10 (7), pp. 4279-4296. Date of Electronic Publication: 2024 Jun 13.
DOI: 10.1021/acsbiomaterials.4c00229
Abstrakt: After traumatic brain injury, the brain extracellular matrix undergoes structural rearrangement due to changes in matrix composition, activation of proteases, and deposition of chondroitin sulfate proteoglycans by reactive astrocytes to produce the glial scar. These changes lead to a softening of the tissue, where the stiffness of the contusion "core" and peripheral "pericontusional" regions becomes softer than that of healthy tissue. Pioneering mechanotransduction studies have shown that soft substrates upregulate intermediate filament proteins in reactive astrocytes; however, many other aspects of astrocyte biology remain unclear. Here, we developed a platform for the culture of cortical astrocytes using polyacrylamide (PA) gels of varying stiffness (measured in Pascal; Pa) to mimic injury-related regions in order to investigate the effects of tissue stiffness on astrocyte reactivity and morphology. Our results show that substrate stiffness influences astrocyte phenotype; soft 300 Pa substrates led to increased GFAP immunoreactivity, proliferation, and complexity of processes. Intermediate 800 Pa substrates increased Aggrecan + , Brevican + , and Neurocan + astrocytes. The stiffest 1 kPa substrates led to astrocytes with basal morphologies, similar to a physiological state. These results advance our understanding of astrocyte mechanotransduction processes and provide evidence of how substrates with engineered stiffness can mimic the injury microenvironment.
Databáze: MEDLINE