Sugai Yuki, Hamai Ryo, Shiwaku Yukari, Anada Takahisa, Tsuchiya Kaori, Kimura Tai, Tadano Manami, Yamauchi Kensuke, Takahashi Tetsu, Egusa Hiroshi, Suzuki Osamu
Division of Craniofacial Function Engineering (Division of Biomaterials Science and Engineering), Tohoku University Graduate School of Dentistry, Sendai 980-8575, Japan.
Division of Oral and Maxillofacial Reconstructive Surgery, Tohoku University Graduate School of Dentistry, Sendai 980-8575, Japan.
Biomimetics (Basel). 2025 Mar 26;10(4):205. doi: 10.3390/biomimetics10040205.
Octacalcium phosphate (OCP) has been shown to exhibit an osteogenic property and, therefore, has been utilized recently as a bone substitute, clinically. However, the stimulatory capacity for induced pluripotent stem (iPS) cells is not known. This study investigated whether OCP enhances osteoblastic differentiation of three-dimensionally cultured spheroids of iPS cells compared to hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP). Mouse iPS cells were mixed with smaller (less than 53 μm) or larger (300-500 μm) sizes of calcium phosphate (CaP) granules and cultured in a laboratory-developed oxygen-permeable culture chip under minimizing hypoxia for up to 21 days. Osteoblastic differentiation was estimated by the cellular alkaline phosphatase (ALP) activities. The degree of supersaturation (DS) with respect to CaP phases was determined from the media chemical compositions. Incubated CaP materials were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The culture promoted well the formation of hybrid spheroids of CaP materials and iPS cells regardless of the type of materials and their granule sizes. The ALP activity of OCP was about 1.5 times higher than that of β-TCP and HA in smaller granule sizes. FTIR, XRD, and DS analyses showed that larger OCP granules tended to hydrolyze to HA slightly faster than smaller granules with time while HA and β-TCP materials tended to remain unchanged. In conclusion, the results suggest that OCP enhances the osteogenic differentiation of iPS cells more than HA and β-TCP through a mechanism of hydrolyzing to HA. This inherent material property of OCP is essential for enhancing the osteoblastic differentiation of iPS cells.
八钙磷酸酯(OCP)已被证明具有成骨特性,因此最近在临床上被用作骨替代物。然而,其对诱导多能干细胞(iPS细胞)的刺激能力尚不清楚。本研究调查了与羟基磷灰石(HA)和β - 磷酸三钙(β - TCP)相比,OCP是否能增强iPS细胞三维培养球体的成骨分化。将小鼠iPS细胞与较小尺寸(小于53μm)或较大尺寸(300 - 500μm)的磷酸钙(CaP)颗粒混合,并在实验室开发的透氧培养芯片中培养,在尽量减少缺氧的条件下培养长达21天。通过细胞碱性磷酸酶(ALP)活性评估成骨分化。根据培养基化学成分确定相对于CaP相的过饱和度(DS)程度。通过傅里叶变换红外光谱(FTIR)和X射线衍射(XRD)对孵育后的CaP材料进行表征。无论材料类型及其颗粒大小如何,该培养均能很好地促进CaP材料与iPS细胞杂交球体的形成。在较小颗粒尺寸下,OCP的ALP活性比β - TCP和HA高约1.5倍。FTIR、XRD和DS分析表明,随着时间的推移,较大的OCP颗粒比较小的颗粒更容易稍微快一点水解为HA,而HA和β - TCP材料则倾向于保持不变。总之,结果表明OCP通过水解为HA的机制比HA和β - TCP更能增强iPS细胞的成骨分化。OCP的这种固有材料特性对于增强iPS细胞的成骨分化至关重要。