Abstract

Hyaline cartilage is a tissue of very low regenerative capacity because of its histology and limited nutrient supply. Cell-based therapies have been spotlighted in the regeneration of damaged cartilage. Dental pulp stem cells (DPSCs) are multipotent and are easily accessible for therapeutic purposes. In human gastrointestinal tracts, Enterococcus faecium is a naturally occurring commensal species of lactic acid bacteria. In this work, the human DPSCs were differentiated into chondrocytes using a chondrogenic differentiation medium with or without L-15 extract. We observed that chondrogenic differentiation improved in an E. faecium L-15 extract (L-15)-treated DPSC group via evaluation of chondrogenic-marker mRNA expression levels. In particular, we found that L-15 treatment promoted early-stage DPSC differentiation. Cells treated with L-15 were inhibited at later stages and were less likely to transform into hypertrophic chondrocytes. In L-15-treated groups, the total amount of cartilage extracellular matrix increased during the differentiation process. These results suggest that L-15 promotes chondrogenic differentiation, and that L-15 may be used for cartilage repair or cartilage health supplements. To our knowledge, this is the first report demonstrating the beneficial effect of L-15 treatment on chondrogenic differentiation.

Highlights

  • Hyaline cartilage is composed of chondrocytes and extracellular matrix, including collagen, proteoglycans, and hyaluronic acid

  • Inortehoivsesrt,utdoyo, uwrekinnovweslteidggatee,dthtehreeiamrepancot orefpEo.rftasecoinumthLe-e1f5feecxttsraocft LoAnBchoonncdarrotiglaegneicddififefererenntitaiatitoionn. .In this study, we investigated the impact of E. faecium L-15 extract on chondrogenic differentiation

  • We found that the L-15 extract initially promoted chondrogenic differentiation and subsequently inhibited the expression of the extracellular matrix degradation enzyme

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Summary

Introduction

Hyaline cartilage is composed of chondrocytes and extracellular matrix, including collagen, proteoglycans, and hyaluronic acid. Because of its avascular and aneural character (which makes it difficult to regenerate when damaged), cell-based therapy is an optimal treatment. This is seen when autologous chondrocytes are implanted in a damaged area [1,2]. Autologous chondrocyte implantation (ACI) is unlikely to cause immune rejection and is effective in treating cartilage defects [3,4]. The number of chondrocytes in the body is low, and there are limited chondrocytes available for use [5]. Due to the substantial limitations of ACI, mesenchymal stem cells (MSCs) are getting spotlight as a cell source for cartilage repair [1,6,7]

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