4.5 Article

Matrix Metalloproteases from Adipose Tissue-Derived Stromal Cells Are Spatiotemporally Regulated by Hydrogel Mechanics in a 3D Microenvironment

Journal

BIOENGINEERING-BASEL
Volume 9, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/bioengineering9080340

Keywords

adipose tissue-derived stromal cells; matrix metalloproteases; hydrogels; GelMA; stiffness; stress relaxation

Funding

  1. Mexican National Council of Science and Technology (CONACyT) [CVU 695528]
  2. De Cock-Hadders foundation [2021-16]
  3. Rosalind Franklin Fellowship
  4. University of Groningen
  5. European Union

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Adipose tissue-derived stromal cells (ASCs) are a promising research subject in tissue engineering and regenerative medicine due to their easy acquisition, multipotency, and secretion of factors promoting tissue regeneration. However, their retention in or around lesions after direct administration is poor. To address this issue, ASCs can be "immobilized" in hydrogels such as gelatine methacryloyl (GelMA). This study found that the concentration of GelMA can influence the expression of matrix metalloproteases (MMPs) secreted by ASCs, as well as their morphology and the ultrastructure of the hydrogel.
Adipose tissue-derived stromal cells (ASCs) are of interest in tissue engineering and regenerative medicine (TERM) due to their easy acquisition, multipotency, and secretion of a host of factors that promote regeneration. Retention of ASCs in or around lesions is poor following direct administration. Therefore, for TERM applications, ASCs can be 'immobilized' via their incorporation into hydrogels such as gelatine methacryloyl (GelMA). Tweaking GelMA concentration is a common approach to approximate the mechanical properties found in organs or tissues that need repair. Distinct hydrogel mechanics influence the ability of a cell to spread, migrate, proliferate, and secrete trophic factors. Mesenchymal cells such as ASCs are potent remodellers of the extracellular matrix (ECM). Not only do ASCs deposit components, they also secrete matrix metalloproteases (MMPs) which degrade ECM. In this work, we investigated if GelMA polymer concentration influenced the expression of active MMPs by ASCs. In addition, MMPs' presence was interrogated with regard to ASCs morphology and changes in hydrogel ultrastructure. For this, immortalised ASCs were embedded in 5%, 10%, and 15% (w/v) GelMA hydrogels, photopolymerised and cultured for 14 d. Zymography in situ indicated that MMPs had a variable, hydrogel concentration-dependent influence on ASCs-secreted MMPs. In 5% GelMA, ASCs showed a high and sustained expression of MMPs, while, in 10% and 15% GelMA, such expression was almost null. ASCs morphology based on F-actin staining showed that increasing GelMA concentrations inhibit their spreading. Scanning electron microscopy (SEM) showed that hydrogel ultrastructure in terms of pore density, pore size, and percentage porosity were not consistently influenced by cells. Interestingly, changes in ultrastructural parameters were detected also in cell-free materials, albeit without a clear trend. We conclude that hydrogel concentration and its underlying mechanics influenced MMP expression by ASCs. The exact MMPs that respond to these mechanical cues should be defined in follow-up experiments.

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