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Osteogenic Differentiation Potential of Equine Dental Pulp vs. Periodontal Ligament Stem Cells: A Comparative In Vitro Study

Jurnal Medik Veteriner · Vol. 8 No. 2 (2025) · hlm. 262–272

DOI
10.20473/jmv.vol8.iss2.2025.262-272
ISSN
2581-012X, 2615-7497
Terbit
2025-10-01
Penerbit
Universitas Airlangga
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-nc-sa/4.0

Abstrak

Equine mesenchymal stem cells (MSCs) are promising for bone tissue engineering (BTE) because of their capabilities of differentiating into osteoblasts. Cell therapy using equine MSCs has been introduced. Recently, dental-derived MSCs have gained significant attention due to their capabilities and ease of collection with minimally invasive collection methods. Dental stem cells show high plasticity, accessibility, and applicability for regenerative medicine and are thus considered alternative sources of MSCs. This study evaluated the characterization, osteogenic differentiation potential, and migration assay of equine dental pulp stem cells (eDPSCs) as compared with equine periodontal ligament stem cells (ePDLSCs). Equine dental stem cells from eDPSCs and ePDLSCs (n = 4) were isolated and expanded to passage 3. The morphology, colony-forming capability, cell proliferation assay, stemness and surface markers, trilineage differentiation potential, and migration assay were investigated in vitro. Both eDPSCs and ePDLSCs exhibited a fibroblast-like morphology; showed a colony-forming capability; were able to proliferate based on the results of the cell proliferation assay; expressed stemness and surface markers (NANOG, CD29, CD44, CD90, CD18); maintained the ability to differentiate into osteocytes, chondrocytes, and adipocytes and demonstrated migration capacity based on the migration assay. Surprisingly, ePDLSCs showed significant differences in matrix mineralization, quantification of Alizarin Red staining by cetylpyridinium chloride, and mRNA expression of the osteogenic marker RUNX2. ePDLSCs and eDPSCs may be better alternative MSCs than dental stem cells for the further design of therapeutic regimens for BTE and wound-healing therapy.

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Michael KannAfiliasi tidak diketahui4
Warih Pulung NugrahaniAfiliasi tidak diketahui4
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Irhamna PutriAfiliasi tidak diketahui3
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Tri WibawaUniversitas Gadjah Mada1
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Sumber metadata: OAI-PMH (metadata jurnal) https://e-journal.unair.ac.id/JMV/oai, pertama di-harvest 9 Nov 2026, terakhir terlihat 9 Nov 2026.
Metadata asli (oai_dc) 
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	<dc:title xml:lang="en-US">Osteogenic Differentiation Potential of Equine Dental Pulp vs. Periodontal Ligament Stem Cells: A Comparative In Vitro Study</dc:title>
	<dc:creator>Purwaningrum, Medania</dc:creator>
	<dc:creator>Haryanto, Aris</dc:creator>
	<dc:creator>Kayanaveda, Yohanna </dc:creator>
	<dc:creator>Sawangmake, Chenphop</dc:creator>
	<dc:subject xml:lang="en-US">bone tissue engineering</dc:subject>
	<dc:subject xml:lang="en-US">equine dental pulp stem cells</dc:subject>
	<dc:subject xml:lang="en-US">equine mesenchymal stem cells</dc:subject>
	<dc:subject xml:lang="en-US">equine periodontal ligament stem cells</dc:subject>
	<dc:subject xml:lang="en-US">osteogenic differentiation potential</dc:subject>
	<dc:description xml:lang="en-US">Equine mesenchymal stem cells (MSCs) are promising for bone tissue engineering (BTE) because of their capabilities of differentiating into osteoblasts. Cell therapy using equine MSCs has been introduced. Recently, dental-derived MSCs have gained significant attention due to their capabilities and ease of collection with minimally invasive collection methods. Dental stem cells show high plasticity, accessibility, and applicability for regenerative medicine and are thus considered alternative sources of MSCs. This study evaluated the characterization, osteogenic differentiation potential, and migration assay of equine dental pulp stem cells (eDPSCs) as compared with equine periodontal ligament stem cells (ePDLSCs). Equine dental stem cells from eDPSCs and ePDLSCs (n = 4) were isolated and expanded to passage 3. The morphology, colony-forming capability, cell proliferation assay, stemness and surface markers, trilineage differentiation potential, and migration assay were investigated in vitro. Both eDPSCs and ePDLSCs exhibited a fibroblast-like morphology; showed a colony-forming capability; were able to proliferate based on the results of the cell proliferation assay; expressed stemness and surface markers (NANOG, CD29, CD44, CD90, CD18); maintained the ability to differentiate into osteocytes, chondrocytes, and adipocytes and demonstrated migration capacity based on the migration assay. Surprisingly, ePDLSCs showed significant differences in matrix mineralization, quantification of Alizarin Red staining by cetylpyridinium chloride, and mRNA expression of the osteogenic marker RUNX2. ePDLSCs and eDPSCs may be better alternative MSCs than dental stem cells for the further design of therapeutic regimens for BTE and wound-healing therapy.</dc:description>
	<dc:publisher xml:lang="en-US">Universitas Airlangga</dc:publisher>
	<dc:date>2025-10-01</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:format>text/xml</dc:format>
	<dc:identifier>https://e-journal.unair.ac.id/JMV/article/view/69445</dc:identifier>
	<dc:identifier>10.20473/jmv.vol8.iss2.2025.262-272</dc:identifier>
	<dc:source xml:lang="en-US">Jurnal Medik Veteriner; Vol. 8 No. 2 (2025): October; 262-272</dc:source>
	<dc:source>2581-012X</dc:source>
	<dc:source>2615-7497</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://e-journal.unair.ac.id/JMV/article/view/69445/34055</dc:relation>
	<dc:relation>https://e-journal.unair.ac.id/JMV/article/view/69445/35256</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2025 Medania Purwaningrum, Aris Haryanto, Yohanna  Kayanaveda, Chenphop Sawangmake</dc:rights>
	<dc:rights xml:lang="en-US">http://creativecommons.org/licenses/by-nc-sa/4.0</dc:rights>
</oai_dc:dc>