Effect of Fibrillin-2 on Differentiation into Periodontal Ligament Stem Cell-Like Cells Derived from Human-Induced Pluripotent Stem Cells.

Stem cells and development Pub Date : 2024-05-01 Epub Date: 2024-04-13 DOI:10.1089/scd.2024.0013
Sayuri Hamano, Diaki Yamashita, Daigaku Hasegawa, Hideki Sugii, Tomohiro Itoyama, Hidefumi Maeda
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Abstract

Periodontal tissue regeneration is important for preserving teeth. Periodontal ligament stem cells (PDLSCs) are useful in periodontal tissue regeneration; however, tooth extraction is required to obtain these cells. Therefore, we focused on induced pluripotent stem (iPS) cells and established a method to obtain PDLSC-like cells from iPS cells. Specifically, we first differentiated iPS cells into neural crest-like cells (iNCs). Next, we obtained PDLSC-like cells (iPDLSCs) by culturing iNCs on extracellular matrix (ECM) derived from human primary periodontal ligament cells (HPDLCs). This differentiation method suggested that ECM derived from HPDLCs is important for iPDLSC differentiation. Thus, we aimed to identify the PDLSC-inducing factor present in HPDLC-derived ECM in this study. We first performed comprehensive analyses of HPDLC genes and identified fibrillin-2 (FBN2), an ECM-related factor. Furthermore, to clarify the effect of FBN2 on iPDLSC differentiation, we cultured iNCs using ECM derived from HPDLCs with FBN2 knocked down. As a result, expression of PDL-related markers was reduced in iNCs cultured on ECM derived from HPDLCs transfected with FBN2 siRNA (iNC-siFBN2) compared with iPDLSCs. Furthermore, the expression of CD105 (a mesenchymal stem cell marker), proliferation ability, and multipotency of iNC-siFBN2 were lower compared with iPDLSCs. Next, we cultured iNCs on FBN2 recombinant protein; however, expression of PDL-related markers did not increase compared with iPDLSC. The present results suggest the critical involvement of FBN2 in inducing iPDLSCs from iNCs when in fact it does not promote iPDLSC differantiation. Therefore, we need to elucidate the entire HPDLC-ECMs, responsible for iPDLSCs induction.

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纤连蛋白-2对人类诱导多能干细胞分化成牙周韧带干细胞样细胞的影响。
牙周组织再生对保护牙齿非常重要。牙周韧带干细胞(PDLSCs)可用于牙周组织再生,但要获得这些细胞必须拔牙。因此,我们将重点放在诱导多能干细胞(iPS)上,并建立了一种从 iPS 细胞中获得 PDLSC 样细胞的方法。具体来说,我们首先将iPS细胞分化成神经嵴样细胞(iNCs)。接着,我们通过在源自人类原代牙周韧带细胞(HPDLCs)的细胞外基质(ECM)上培养 iNCs 获得了 PDLSC 样细胞(iPDLSCs)。这种分化方法表明,源自 HPDLCs 的 ECM 对 iPDLSC 的分化非常重要。因此,本研究旨在确定 HPDLC 衍生 ECM 中的 PDLSC 诱导因子。我们首先对 HPDLC 基因进行了全面分析,发现了与 ECM 相关的因子--纤连蛋白-2(FBN2)。此外,为了明确 FBN2 对 iPDLSC 分化的影响,我们使用敲除 FBN2 的 HPDLC 衍生 ECM 培养 iNCs。结果发现,与 iPDLSCs 相比,在转染了 FBN2 siRNA 的 HPDLCs(iNC-siFBN2)ECM 上培养的 iNCs 中,PDL 相关标记物的表达减少了。此外,与 iPDLSCs 相比,iNC-siFBN2 的 CD105(间充质干细胞标志物)表达、增殖能力和多能性都较低。接着,我们用 FBN2 重组蛋白培养 iNC,但与 iPDLSC 相比,PDL 相关标记物的表达并没有增加。本研究结果表明,FBN2 在从 iNCs 诱导 iPDLSCs 的过程中起着关键作用,但它本身并没有促进作用。因此,我们需要阐明负责诱导 iPDLSCs 的整个 HPDLC-ECMs。
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