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Journal Article

Analogies and Differences Between Dental Stem Cells: Focus on Secretome in Combination with Scaffolds in Neurological Disorders

Francesca Santilli; Jessica Fabrizi; Costantino Santacroce; Daniela Caissutti; Zaira Spinello; Niccolò Candelise; Loreto Lancia; Fanny Pulcini; Simona Delle Monache; Vincenzo Mattei
Stem Cell Reviews and Reports · Vol. 20, Issue 1 · pp. 159-174 · 2024

Abstract

Mesenchymal stem cells (MSCs) are well known for their beneficial effects, differentiation capacity and regenerative potential. Dental-derived MSCs (DSCs) are more easily accessible and have a non-invasive isolation method rather than MSCs isolated from other sources (umbilical cord, bone marrow, and adipose tissue). In addition, DSCs appear to have a relevant neuro-regenerative potential due to their neural crest origin. However, it is now known that the beneficial effects of MSCs depend, at least in part, on their secretome, referring to all the bioactive molecules (neurotrophic factors) released in the conditioned medium (CM) or in the extracellular vesicles (EVs) in particular exosomes (Exos). In this review, we described the similarities and differences between various DSCs. Our focus was on the secretome of DSCs and their applications in cell therapy for neurological disorders. For neuro-regenerative purposes, the secretome of different DSCs has been tested. Among these, the secretome of dental pulp stem cells and stem cells from human exfoliated deciduous teeth have been the most widely studied. Both CM and Exos obtained from DSCs have been shown to promote neurite outgrowth and neuroprotective effects as well as their combination with scaffold materials (to improve their functional integration in the tissue). For these reasons, the secretome obtained from DSCs in combination with scaffold materials may represent a promising tissue engineering approach for neuroprotective and neuro-regenerative treatments. Graphical Abstract

Bibliographic Information

JournalStem Cell Reviews and Reports
PublisherSpringer
Publication Date2024-01-01
Publication Year2024
Volume20
Issue1
Pages159-174
Document TypeJournal Article
Print ISSN2629-3269
eISSN2629-3277
DOI10.1007/s12015-023-10652-9

Access Information

NARA Access Coverage2005-01-01~Current
Journal Homepagehttps://www.springer.com/journal/12015
Publisher PageOpen Publisher Page
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