从无喂养培养的诱导多能干细胞中建立牙周韧带干细胞样细胞

Daiki Yamashita, Sayuri Hamano, Daigaku Hasegawa, Hideki Sugii, Tomohiro Itoyama, Makoto Ikeya, Hidefumi Maeda
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引用次数: 0

摘要

牙周韧带(PDL)是连接牙根骨水泥和牙槽骨的纤维结缔组织。牙周韧带中含有的牙周韧带干细胞(PDLSCs)可分化为骨水泥母细胞、成骨细胞和牙周韧带成纤维细胞,在牙周组织再生中发挥重要作用。因此,PDLSCs有望在牙周组织再生治疗中发挥作用。在之前的一项研究中,我们将诱导多能干细胞(iPSCs)分化成了 PDLSC 样细胞(iPDLSCs),这些细胞表达 PDL 相关标记和间充质干细胞(MSC)标记;它们还表现出高增殖性和多潜能性。然而,这种分化方法中使用的 iPSCs 是在小鼠胚胎成纤维细胞上培养的,因此构成了馈源 iPSCs(OF-iPSCs)。考虑到饲养细胞衍生成分污染的风险,由OF-iPSCs分化出的iPDLSCs(即OF-iPDLSCs)不适合临床应用。在本研究中,我们旨在利用 OF-iPDLSC 分化方法从无供养细胞的 iPSCs(FF-iPSCs)中获得 PDLSC 样细胞。首先,我们将 FF-iPSCs 分化成神经嵴细胞样细胞(FF-iNCCs),并确认 FF-iNCCs 表达 NCC 标记(如 Nestin 和 p75NTR)。然后,我们将 FF-iNCCs 在源于人类原代 PDL 细胞的细胞外基质上培养了 2 周,得到的细胞被命名为 FF-iPDLSCs。与 OF-iPDLSCs 相比,FF-iPDLSCs 表现出更高的 PDL 相关标记和间充质干细胞标记表达。FF-iPDLSCs 在体外也表现出增殖和多潜能性。最后,我们分析了 FF-iPDLSCs 与 β-磷酸三钙支架一起皮下移植到免疫缺陷小鼠背侧组织后在体内形成牙周组织的能力。移植八周后,FF-iPDLSCs 形成了骨钙素阳性的骨/骨灰质样组织和胶原 1 阳性的 PDL 样纤维。这些结果表明,我们成功地从 FF-iPSCs 中获得了 PDLSC 样细胞。我们的研究结果将有助于开发新型牙周再生疗法。
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Establishment of Periodontal Ligament Stem Cell-like Cells Derived from Feeder-Free Cultured Induced Pluripotent Stem Cells.

The periodontal ligament (PDL) is a fibrous connective tissue that connects the cementum of the root to the alveolar bone. PDL stem cells (PDLSCs) contained in the PDL can differentiate into cementoblasts, osteoblasts, and PDL fibroblasts, with essential roles in periodontal tissue regeneration. Therefore, PDLSCs are expected to be useful in periodontal tissue regeneration therapy. In a previous study, we differentiated induced pluripotent stem cells (iPSCs) into PDLSC-like cells (iPDLSCs), which expressed PDL-related markers and mesenchymal stem cell (MSC) markers; they also exhibited high proliferation and multipotency. However, the iPSCs used in this differentiation method were cultured on mouse embryonic fibroblasts; thus, they constituted on-feeder iPSCs (OF-iPSCs). Considering the risk of contamination with feeder cell-derived components, iPDLSCs differentiated from OF-iPSCs (ie, OF-iPDLSCs) are unsuitable for clinical applications. In this study, we aimed to obtain PDLSC-like cells from feeder-free iPSCs (FF-iPSCs) using OF-iPDLSC differentiation method. First, we differentiated FF-iPSCs into neural crest cell-like cells (FF-iNCCs) and confirmed that FF-iNCCs expressed NCC markers (eg, Nestin and p75NTR). Then, we cultured FF-iNCCs on human primary PDL cell-derived extracellular matrix for 2 weeks; the resulting cells were named FF-iPDLSCs. FF-iPDLSCs exhibited higher expression of PDL-related and MSC markers compared with OF-iPDLSCs. FF-iPDLSCs also demonstrated proliferation and multipotency in vitro. Finally, we analyzed the ability of FF-iPDLSCs to form periodontal tissue in vivo upon subcutaneous transplantation with β-tricalcium phosphate scaffolds into dorsal tissues of immunodeficient mice. Eight weeks after transplantation, FF-iPDLSCs had formed osteocalcin-positive bone/cementum-like tissues and collagen 1-positive PDL-like fibers. These results suggested that we successfully obtained PDLSC-like cells from FF-iPSCs. Our findings will contribute to the development of novel periodontal regeneration therapies.

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Advancements in Organoid Culture Technologies: Current Trends and Innovations. Establishment of Periodontal Ligament Stem Cell-like Cells Derived from Feeder-Free Cultured Induced Pluripotent Stem Cells. Safety and Potential Efficacy of Expanded Umbilical Cord-Derived Mesenchymal Stromal Cells in Luminal Ulcerative Colitis Patients. Development of Mesenchymal Stem Cell Encoded with Myogenic Gene for Treating Radiation-Induced Muscle Fibrosis. Dtx2 Deficiency Induces Ependymo-Radial Glial Cell Proliferation and Improves Spinal Cord Motor Function Recovery.
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