4.5 Article

Pro-angiogenic potential of a functionalized hydrogel scaffold as a secretome delivery platform: An innovative strategy for cell homing-based dental pulp tissue engineering

Journal

Publisher

WILEY
DOI: 10.1002/term.3294

Keywords

angiogenesis; dental pulp; hydrogel scaffold; stem cells secretome; tissue engineering

Funding

  1. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [2018/01501-7, 2018/14694-8, 2019/19066-8]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [235015/2014-8, 306423/2018-9]

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Angiogenesis is a crucial process in tissue engineering, but faces challenges in regenerative endodontic procedures. This study explores a functionalized chitosan hydrogel scaffold loaded with secretomes from stem cells as a platform for cell homing-based tissue engineering. The results show that the functionalized scaffold can sustainably release trophic factors, leading to improved cell proliferation, chemotaxis, and angiogenesis. Thus, this functionalized scaffold holds promise in promoting tissue engineering through cell homing approaches.
Angiogenesis is a key process that provides a suitable environment for successful tissue engineering and is even more crucial in regenerative endodontic procedures, since the root canal anatomy limits the development of a vascular network supply. Thus, sustainable and accelerated vascularization of tissue-engineered dental pulp constructs remains a major challenge in cell homing approaches. This study aimed to functionalize a chitosan hydrogel scaffold (CS) as a platform loaded with secretomes of stem cells from human exfoliated deciduous teeth (SHEDs) and evaluate its bioactive function and pro-angiogenic properties. Initially, the CS was loaded with SHED secretomes (CS-S), and the release kinetics of several trophic factors were assessed. Proliferation and chemotaxis assays were performed to analyze the effect of functionalized scaffold on stem cells from apical papilla (SCAPs) and the angiogenic potential was analyzed through the Matrigel tube formation assay with co-cultured of human umbilical vein endothelial cells and SCAPs. SHEDs and SCAPs expressed typical levels of mesenchymal stem cell surface markers. CS-S was able to release the trophic factors in a sustained manner, but each factor has its own release kinetics. The CS-S group showed a significantly higher proliferation rate, accelerated the chemotaxis, and higher capacity to form vascular-like structures. CS-S provided a sustained and controlled release of trophic factors, which, in turn, improved proliferation, chemotaxis and all angiogenesis parameters in the co-culture. Thus, the functionalization of chitosan scaffolds loaded with secretomes is a promising platform for cell homing-based tissue engineering.

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