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Coagulative Granular Hydrogels with an Enzyme Catalyzed Fibrin Network for Endogenous Tissue Regeneration

Zhipeng Deng, Camila B. Tovani, Simona Bianco, Gianni Comandini, Aya Elghajiji, Dave J. Adams, Fabrizio Scarpa, Michael R. Whitehouse, Annela M. Seddon, James P. K. Armstrong

Posted on: 6 January 2025

Preprint posted on 21 November 2024

Fibrin gels to glue granular units

Selected by Castro Johnbosco

Categories: bioengineering

Background

Tissue engineering has largely relied on engineered hydrogels that have cellular units to fabricate tissue like constructs. These hydrogel matrices are certainly made up of polymer biomaterials (natural or synthetic) with tunable properties. Often these hydrogel matrices are bulk and macro in size which makes them harder to inject, especially for in situ applications. Hence a relatively new class of material design known as granular hydrogels has come to the forefront to overcome the limitation of bulk hydrogel matrices. However, these granular systems often possess weak mechanical stability, due to interstitial void formation and poor injectability.

In this preprint the authors report a new approach to stabilize the interstitial porosity-driven mechanical instability different from previously reported methods like photo annealing, and dynamic chemistries, including host-guest interactions. The resulting coagulant granular hydrogels use surface-functionalized thrombin to catalyze fibrinogen-to-fibrin conversion that glues granular units together to form a cell-laden scaffold

Key findings

Thrombin as an effective catalyzer of fibrinogen to glue granular microgel units

First the authors functionalized thrombin onto the microgel surface using surface modification of GelMA granular hydrogels. The controlled thrombin functionalization reported in this study is highly tunable and the enzymatic activity can be upscaled depending on the requirements. The thrombin-functionalized granular microgel units were used as active catalyzers to engulf the surrounding fibrinogen into fibrin gel to promote cellular infiltration.

 

Interconnecting stability-induced enhancement in scaffold mechanics

The inter-microgel gluing created by fibrinogen-converted fibrin gel enhanced the total mechanics of the scaffold. The total shear modulus of this modular scaffold was (~1.5 fold) increased compared to the bulk hydrogels’ mechanical property. Moreover, the modular coagulative scaffold that was formed had enhanced injectability suitable for in-situ injectable granular systems.

 

Fibrin glue promoted cellular infiltration and vascular sprouting

The authors validated the cellular adaptability of interstitial fibrin glue between the granular microgel units by assessing the activity of human umbilical vein endothelial cells (HUVECs). The modular scaffold with fibrin-glued granular units revealed enhanced cell proliferation with higher metabolic activity and more cell spreading compared to control conditions. To check the robustness of this modular design, the authors further explored controlled vascular sprouting through the fibrin-glued interstitial space. Multicellular spheroids with HUVECs and MSCs (mesenchymal stem cells) exhibited enhanced vascular sprouting compared to conditions without fibrinogen with an outgrowth of (5.6 fold) respectively.

 

 

Why do I like this preprint ?

This work denotes a scalable and injectable granular system that can provide mechanical stability to the scaffold. Moreover, such a modular design with enhanced vascular endothelial sprouting can aid vascularization when injected in vivo. Even though, thrombin cross-linkable hydrogels have been established previously but the concept of gluing granular systems using thrombin as a catalyzer is novel and can open up new ways in jam-packed granular microgel applications.

Tags: coagulant, granular

doi: https://doi.org/10.1242/prelights.39028

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Author's response

James P. K. Armstrong shared

As the title suggests coagulative granular systems, how do you imagine interaction with blood would influence the bulk mechanics of the formed granular scaffold?

The biomaterial was designed to mechanically stabilize following interaction with blood, an approach that was inspired by fibrin formation during the final stage of blood clotting. We functionalized the granular hydrogel with thrombin to allow it to catalyze fibrinogen (present in blood plasma) into a fibrin network that can “glue” the microgels together. The fibrinogen concentration was chosen to match the acute inflammatory phase, and our compression tests showed that the formation of fibrin could mechanically stabilize the granular hydrogel to the level of the bulk hydrogel.

As fibrin is degradable have you looked into degradation profiles and will it influence the long-term stability of the proposed granular scaffold?

Although fibrin is degradable, we hypothesize that the fibrinogen-rich in vivo environment will allow the surface-bound thrombin to catalyze the formation of new fibrin networks. This hypothesis would need to be tested with in vivo studies. On the other hand, in vitro cell studies would most likely require the use of antifibrinolytic supplements (e.g., aminocaproic acid) that are commonly used to slow the degradation of fibrin.

What is the reaction time of thrombin-catalyzed conversion of fibrinogen to fibrin and how can it influence the in vivo applicability?

In this study, we observed the formation of fibrin fibrils at very early timepoints (less than an hour), with a stable fibrin gel forming after an overnight incubation at 37°C. This rate was optimal for our study, however, we also showed that the catalytic reaction rate can be modulated by altering the degree of thrombin functionalization. This tunability should allow broad applications but the optimal rate for stabilization and tissue regeneration may need to be determined through in vivo studies.

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