Fabrication and Characterization of Quad-Component Bioinspired Hydrogels to Model Elevated Fibrin Levels in Central Nervous Tissue Scaffolds

Author:

Diaz-Lasprilla Ana M.1ORCID,McKee Meagan1,Jimenez-Vergara Andrea C.1,Ravi Swathisri2,Bellamy Devon3,Ortega Wendy1,Crosby Cody O.4ORCID,Steele Jennifer5ORCID,Plascencia-Villa Germán6,Perry George6ORCID,Munoz-Pinto Dany J.17ORCID

Affiliation:

1. Engineering Science Department, D. R. Semmes School of Science, Trinity University, San Antonio, TX 78212, USA

2. Biology Department, D. R. Semmes School of Science, Trinity University, San Antonio, TX 78212, USA

3. Chemistry Department, D. R. Semmes School of Science, Trinity University, San Antonio, TX 78212, USA

4. Department of Physics, Southwestern University, Georgetown, TX 78626, USA

5. Physics and Astronomy Department, D. R. Semmes School of Science, Trinity University, San Antonio, TX 78212, USA

6. Department of Neuroscience, Developmental and Regenerative Biology, College of Sciences, The University of Texas at San Antonio (UTSA), San Antonio, TX 78249, USA

7. Neuroscience Program, D. R. Semmes School of Science, Trinity University, San Antonio, TX 78212, USA

Abstract

Multicomponent interpenetrating polymer network (mIPN) hydrogels are promising tissue-engineering scaffolds that could closely resemble key characteristics of native tissues. The mechanical and biochemical properties of mIPNs can be finely controlled to mimic key features of target cellular microenvironments, regulating cell-matrix interactions. In this work, we fabricated hydrogels made of collagen type I (Col I), fibrin, hyaluronic acid (HA), and poly (ethylene glycol) diacrylate (PEGDA) using a network-by-network fabrication approach. With these mIPNs, we aimed to develop a biomaterial platform that supports the in vitro culture of human astrocytes and potentially serves to assess the effects of the abnormal deposition of fibrin in cortex tissue and simulate key aspects in the progression of neuroinflammation typically found in human pathologies such as Alzheimer’s disease (AD), Parkinson’s disease (PD), and tissue trauma. Our resulting hydrogels closely resembled the complex modulus of AD human brain cortex tissue (~7.35 kPa), promoting cell spreading while allowing for the modulation of fibrin and hyaluronic acid levels. The individual networks and their microarchitecture were evaluated using confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM). Human astrocytes were encapsulated in mIPNs, and negligible cytotoxicity was observed 24 h after the cell encapsulation.

Funder

National Science Foundation

San Antonio Medical Foundation

Trinity University

Publisher

MDPI AG

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