Dental Pulp Stem Cell Conditioned Medium Enhance Osteoblastic Differentiation and Bone Regeneration.

IF 4.5 3区 医学 Q2 CELL & TISSUE ENGINEERING
Batoul Chouaib, Alban Desoutter, Frédéric Cuisinier, Pierre-Yves Collart-Dutilleul
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引用次数: 0

Abstract

Background: Cell-free approaches, utilizing mesenchymal stem cell secretome, have promising prospects in various fields of regenerative medicine. In this study, we examined in vitro and in vivo the potential of dental pulp stem cell-conditioned medium (DPSC-CM) for bone regeneration.

Methods: The secretome of undifferentiated stem cells from dental pulp were collected, and the effects of this DPSC-CM were assessed for osteodifferentiation of osteoblast-like cells (MG-63) and osteoblasts deriving from DPSC. Cell proliferation, alkaline phosphatase (ALP) activity, gene expression of Runt-related transcription factor 2 (Runx2), Bone Sialoprotein (BSP), Osteocalcin (OCN), and extracellular matrix mineralization were evaluated. The rat caudal vertebrae critical size defect model was to investigate the effect of DPSC-CM in vivo.

Results: Results showed that DPSC-CM induced cell growth, and increased ALP activity and the expression of key marker genes at an early stage of osteoblastic differentiation compared to control. A rat bone defect model was used to illustrate the effect of DPSC-CM in vivo. The bone density within the defects were improved using conditioned medium, even though there was no significant difference between the control and DPSC-CM groups. The analysis of DPSC-CM by human growth factor antibody array revealed the presence of several factors involved in osteogenesis.

Conclusion: Taken together, these findings indicate that DPSC-CM is a promising therapeutic candidate for bone regenerative therapy, accelerating the maturation of osteoblastic cells. And even though safety and efficiency of DPSC-CM have to be confirmed in preclinical studies, these results represent a first step toward clinical application.

牙髓干细胞条件培养基可促进成骨细胞分化和骨再生
背景:利用间充质干细胞分泌组的无细胞方法在再生医学的各个领域都具有广阔的前景。在这项研究中,我们在体外和体内研究了牙髓干细胞调节培养基(DPSC-CM)用于骨再生的潜力:方法:我们收集了牙髓中未分化干细胞的分泌物,并评估了这种 DPSC-CM 对成骨细胞样细胞(MG-63)和 DPSC 衍生成骨细胞骨分化的影响。对细胞增殖、碱性磷酸酶(ALP)活性、Runt相关转录因子2(Runx2)、骨硅蛋白(BSP)、骨钙素(OCN)的基因表达以及细胞外基质矿化进行了评估。大鼠尾椎临界大小缺损模型是为了研究 DPSC-CM 在体内的作用:结果表明,与对照组相比,DPSC-CM 在成骨细胞分化的早期阶段能诱导细胞生长、提高 ALP 活性和关键标记基因的表达。大鼠骨缺损模型被用来说明 DPSC-CM 在体内的作用。尽管对照组和 DPSC-CM 组之间没有显著差异,但使用条件培养基后,缺损处的骨密度得到了改善。利用人体生长因子抗体阵列对 DPSC-CM 进行的分析表明,其中存在多种参与成骨的因子:综上所述,这些研究结果表明,DPSC-CM 可加速成骨细胞的成熟,是一种很有前景的骨再生治疗候选疗法。尽管 DPSC-CM 的安全性和有效性还有待临床前研究的证实,但这些结果代表着向临床应用迈出了第一步。
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来源期刊
Stem Cell Reviews and Reports
Stem Cell Reviews and Reports 医学-细胞生物学
CiteScore
9.30
自引率
4.20%
发文量
0
审稿时长
3 months
期刊介绍: The purpose of Stem Cell Reviews and Reports is to cover contemporary and emerging areas in stem cell research and regenerative medicine. The journal will consider for publication: i) solicited or unsolicited reviews of topical areas of stem cell biology that highlight, critique and synthesize recent important findings in the field. ii) full length and short reports presenting original experimental work. iii) translational stem cell studies describing results of clinical trials using stem cells as therapeutics. iv) papers focused on diseases of stem cells. v) hypothesis and commentary articles as opinion-based pieces in which authors can propose a new theory, interpretation of a controversial area in stem cell biology, or a stem cell biology question or paradigm. These articles contain more speculation than reviews, but they should be based on solid rationale. vi) protocols as peer-reviewed procedures that provide step-by-step descriptions, outlined in sufficient detail, so that both experts and novices can apply them to their own research. vii) letters to the editor and correspondence. In order to facilitate this exchange of scientific information and exciting novel ideas, the journal has created five thematic sections, focusing on: i) the role of adult stem cells in tissue regeneration; ii) progress in research on induced pluripotent stem cells, embryonic stem cells and mechanism governing embryogenesis and tissue development; iii) the role of microenvironment and extracellular microvesicles in directing the fate of stem cells; iv) mechanisms of stem cell trafficking, stem cell mobilization and homing with special emphasis on hematopoiesis; v) the role of stem cells in aging processes and cancerogenesis.
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