Derivation of Mesenchymal Stem Cells through Sequential Presentation of Growth Factors via Gelatin Microparticles in Pluripotent Stem Cell Spheroids.

IF 8.1 Q1 ENGINEERING, BIOMEDICAL
Biomaterials research Pub Date : 2025-04-29 eCollection Date: 2025-01-01 DOI:10.34133/bmr.0184
Nityanand Prakash, Young Cha, Won-Gun Koh, Hansoo Park, Alvin Bacero Bello, Soo-Hong Lee
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Abstract

The use of mesenchymal stem cells (MSCs) in regenerative medicine has gained considerable attention in recent years with the development of clinically relevant MSCs from induced pluripotent stem cells (iPSCs) and embryonic stem cells. Through sequential presentations of appropriate growth factors (GFs), iPSCs can be differentiated into mesodermal cells and then into MSCs. Furthermore, the formation of 3-dimensional cell spheroids, known as embryoid bodies, can be used to mimic in vivo conditions. However, the compact nature of embryoid bodies restricts the efficient and uniform delivery of GFs, leading to the formation of necrotic zones and hindered differentiation. To address this, we developed 2 types of gelatin microparticles (GelMPs) with distinct degradation rates for sequential delivery of GFs to enhance differentiation while preventing necrotic zones. In 2-dimensional culture, bone morphogenetic protein-4 (BMP4) and fibroblast growth factor 2 (FGF2) were identified as key proteins inducing iPSC differentiation into mesodermal cells and MSCs. The sequential presentation of these GFs was optimized for a 3-dimensional culture system by engineering fast-degrading GelMPs conjugated with BMP4 and slow-degrading GelMPs conjugated with FGF2. Our approach facilitated efficient iPSC differentiation into induced mesenchymal stem cells (iMSCs), as demonstrated by enhanced expression of mesodermal markers during the early stages of differentiation and MSC-specific markers at later stages. The resulting iMSCs exhibited characteristic surface markers (e.g., CD73, CD90, CD105, and CD44) and trilineage differentiation capability and were genetically stable. Compared to adult-derived MSCs, iMSCs showed superior proliferative capacity and reduced senescence, making them advantageous for cell therapy and regenerative medicine. This innovative approach of generating iMSCs has vast potential for therapeutic applications.

通过明胶微粒在多能干细胞球体中序贯表达生长因子来衍生间充质干细胞。
近年来,随着从诱导多能干细胞(iPSCs)和胚胎干细胞中分离出的具有临床意义的间充质干细胞的发展,间充质干细胞(MSCs)在再生医学中的应用受到了广泛关注。通过适当的生长因子(GFs)的顺序呈现,iPSCs可以分化为中胚层细胞,然后分化为间充质干细胞。此外,三维细胞球体的形成,被称为胚状体,可以用来模拟体内条件。然而,胚状体的致密性限制了GFs的高效和均匀递送,导致坏死带的形成和分化受阻。为了解决这个问题,我们开发了两种具有不同降解率的明胶微粒(GelMPs),用于连续递送gf,以增强分化,同时防止坏死区。在二维培养中,骨形态发生蛋白4 (bone morphogenetic protein-4, BMP4)和成纤维细胞生长因子2 (fibroblast growth factor 2, FGF2)被鉴定为诱导iPSC向中胚层细胞和间充质干细胞分化的关键蛋白。通过与BMP4结合的快速降解GelMPs和与FGF2结合的慢降解GelMPs,在三维培养系统中优化了这些GFs的顺序呈现。我们的方法促进了iPSC向诱导间充质干细胞(iMSCs)的有效分化,在分化的早期阶段,中胚层标记物的表达增强,在分化的后期,msc特异性标记物的表达增强。由此产生的iMSCs具有特征性的表面标记(如CD73、CD90、CD105和CD44)和三龄分化能力,并且具有遗传稳定性。与成人来源的间充质干细胞相比,iMSCs表现出优越的增殖能力和减少衰老,使其在细胞治疗和再生医学中具有优势。这种产生间充质干细胞的创新方法具有巨大的治疗应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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