» Articles » PMID: 18938268

SHED Repair Critical-size Calvarial Defects in Mice

Overview
Journal Oral Dis
Specialty Dentistry
Date 2008 Oct 22
PMID 18938268
Citations 89
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Stem cells from human exfoliated deciduous teeth (SHED) are a population of highly proliferative postnatal stem cells capable of differentiating into odontoblasts, adipocytes, neural cells, and osteo-inductive cells. To examine whether SHED-mediated bone regeneration can be utilized for therapeutic purposes, we used SHED to repair critical-size calvarial defects in immunocompromised mice.

Materials And Methods: We generated calvarial defects and transplanted SHED with hydroxyapatite/tricalcium phosphate as a carrier into the defect areas.

Results: SHED were able to repair the defects with substantial bone formation. Interestingly, SHED-mediated osteogenesis failed to recruit hematopoietic marrow elements that are commonly seen in bone marrow mesenchymal stem cell-generated bone. Furthermore, SHED were found to co-express mesenchymal stem cell marker, CC9/MUC18/CD146, with an array of growth factor receptors such as transforming growth factor beta receptor I and II, fibroblast growth factor receptor I and III, and vascular endothelial growth factor receptor I, implying their comprehensive differentiation potential.

Conclusions: Our data indicate that SHED, derived from neural crest cells, may select unique mechanisms to exert osteogenesis. SHED might be a suitable resource for orofacial bone regeneration.

Citing Articles

Scratch-Based Isolation of Primary Cells (SCIP): A Novel Method to Obtain a Large Number of Human Dental Pulp Cells Through One-Step Cultivation.

Kiyokawa Y, Terajima M, Sato M, Inada E, Hori Y, Bando R J Clin Med. 2024; 13(23).

PMID: 39685514 PMC: 11642068. DOI: 10.3390/jcm13237058.


The Role of Dental-derived Stem Cell-based Therapy and Their Derived Extracellular Vesicles in Post-COVID-19 Syndrome-induced Tissue Damage.

Rostami M, Farahani P, Esmaelian S, Bahman Z, Hussein A, A Alrikabi H Stem Cell Rev Rep. 2024; 20(8):2062-2103.

PMID: 39150646 DOI: 10.1007/s12015-024-10770-y.


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

Santilli F, Fabrizi J, Santacroce C, Caissutti D, Spinello Z, Candelise N Stem Cell Rev Rep. 2023; 20(1):159-174.

PMID: 37962698 PMC: 10799818. DOI: 10.1007/s12015-023-10652-9.


Dental pulp stem cells for reconstructing bone defects: A systematic review and meta-analysis.

Moeenzade N, Naseri M, Osmani F, Emadian Razavi F J Dent Res Dent Clin Dent Prospects. 2023; 16(4):204-220.

PMID: 37560493 PMC: 10407871. DOI: 10.34172/joddd.2022.034.


Potential of Oral Cavity Stem Cells for Bone Regeneration: A Scoping Review.

Alarcon-Apablaza J, Prieto R, Rojas M, Fuentes R Cells. 2023; 12(10).

PMID: 37408226 PMC: 10216382. DOI: 10.3390/cells12101392.


References
1.
Chai Y, Jiang X, Ito Y, Bringas Jr P, Han J, Rowitch D . Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis. Development. 2000; 127(8):1671-9. DOI: 10.1242/dev.127.8.1671. View

2.
Akintoye S, Lam T, Shi S, Brahim J, Collins M, Robey P . Skeletal site-specific characterization of orofacial and iliac crest human bone marrow stromal cells in same individuals. Bone. 2006; 38(6):758-68. DOI: 10.1016/j.bone.2005.10.027. View

3.
Gronthos S, Mankani M, Brahim J, Robey P, Shi S . Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo. Proc Natl Acad Sci U S A. 2000; 97(25):13625-30. PMC: 17626. DOI: 10.1073/pnas.240309797. View

4.
Traver D, Zon L . Walking the walk: migration and other common themes in blood and vascular development. Cell. 2002; 108(6):731-4. DOI: 10.1016/s0092-8674(02)00686-4. View

5.
Mayo K, Griffioen A . Angiostatic proteins and peptides. Crit Rev Eukaryot Gene Expr. 2002; 11(4):319-34. View