Nan Zhang, Li Xu, Hao Song, Chunqing Bu, Jie Kang, Chuanchen Zhang, Xiaofei Yang, Fabin Han
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Magnetic resonance imaging was used to track SHED survival and migration <i>in vivo</i> due to a low-intensity signal artifact caused by MIRB. HE and immunohistochemical analyses revealed that both MIRB-labeled and unlabeled SHED could promote periodontal bone regeneration. The colocalization of hNUC and MIRB demonstrated that SHED transplanted into rats could survive <i>in vivo</i>. Furthermore, some MIRB-positive cells expressed the osteoblast and osteocyte markers OCN and DMP1, respectively. Enzyme-linked immunosorbent assay revealed that SHED could secrete protein factors, such as IGF-1, OCN, ALP, IL-4, VEGF, and bFGF, which promote bone regeneration. Immunofluorescence staining revealed that the transplanted SHED was surrounded by a large number of host-derived Runx2- and Col II-positive cells that played important roles in the bone healing process.</p><p><strong>Conclusions: </strong>SHED could promote periodontal bone regeneration in rats, and the survival of SHED could be tracked <i>in vivo</i> by labeling them with MIRB. 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引用次数: 1
摘要
背景和目的:慢性牙周炎可导致牙槽骨吸收并最终导致牙齿脱落。脱落乳牙干细胞是合适的骨再生种子细胞。在修复牙周骨缺损过程中,采用超顺磁性氧化铁颗粒(SPIO) Molday ION Rhodamine-B (MIRB)对移植细胞进行标记和监测,追踪移植细胞的存活、迁移和分化。方法和结果:我们通过观察标记的SHED的生长和成骨分化来确定合适的MIRB剂量。最后用25 μg Fe/ml MIRB标记SHED,然后移植到大鼠体内。由于MIRB引起的低强度信号伪影,磁共振成像用于跟踪体内SHED的存活和迁移。HE和免疫组化分析显示,mirb标记和未标记的SHED均能促进牙周骨再生。hNUC和MIRB的共定位证明了SHED移植到大鼠体内可以存活。此外,一些mirb阳性细胞分别表达成骨细胞和骨细胞标志物OCN和DMP1。酶联免疫吸附实验显示,SHED可分泌IGF-1、OCN、ALP、IL-4、VEGF、bFGF等促进骨再生的蛋白因子。免疫荧光染色显示移植的SHED被大量宿主来源的Runx2-和Col ii阳性细胞包围,这些细胞在骨愈合过程中发挥重要作用。结论:SHED可促进大鼠牙周骨再生,并可通过MIRB标记来追踪其体内存活情况。SHED可能通过直接分化和旁分泌机制促进骨愈合。
Tracking of Stem Cells from Human Exfoliated Deciduous Teeth Labeled with Molday ION Rhodamine-B during Periodontal Bone Regeneration in Rats.
Background and objectives: Chronic periodontitis can lead to alveolar bone resorption and eventually tooth loss. Stem cells from exfoliated deciduous teeth (SHED) are appropriate bone regeneration seed cells. To track the survival, migration, and differentiation of the transplanted SHED, we used super paramagnetic iron oxide particles (SPIO) Molday ION Rhodamine-B (MIRB) to label and monitor the transplanted cells while repairing periodontal bone defects.
Methods and results: We determined an appropriate dose of MIRB for labeling SHED by examining the growth and osteogenic differentiation of labeled SHED. Finally, SHED was labeled with 25 μg Fe/ml MIRB before being transplanted into rats. Magnetic resonance imaging was used to track SHED survival and migration in vivo due to a low-intensity signal artifact caused by MIRB. HE and immunohistochemical analyses revealed that both MIRB-labeled and unlabeled SHED could promote periodontal bone regeneration. The colocalization of hNUC and MIRB demonstrated that SHED transplanted into rats could survive in vivo. Furthermore, some MIRB-positive cells expressed the osteoblast and osteocyte markers OCN and DMP1, respectively. Enzyme-linked immunosorbent assay revealed that SHED could secrete protein factors, such as IGF-1, OCN, ALP, IL-4, VEGF, and bFGF, which promote bone regeneration. Immunofluorescence staining revealed that the transplanted SHED was surrounded by a large number of host-derived Runx2- and Col II-positive cells that played important roles in the bone healing process.
Conclusions: SHED could promote periodontal bone regeneration in rats, and the survival of SHED could be tracked in vivo by labeling them with MIRB. SHED are likely to promote bone healing through both direct differentiation and paracrine mechanisms.
期刊介绍:
International Journal of Stem Cells (Int J Stem Cells), a peer-reviewed open access journal, principally aims to provide a forum for investigators in the field of stem cell biology to present their research findings and share their visions and opinions. Int J Stem Cells covers all aspects of stem cell biology including basic, clinical and translational research on genetics, biochemistry, and physiology of various types of stem cells including embryonic, adult and induced stem cells. Reports on epigenetics, genomics, proteomics, metabolomics of stem cells are welcome as well. Int J Stem Cells also publishes review articles, technical reports and treatise on ethical issues.