Mehrabani Davood, Sholehvar Fatemeh, Yaghmaei Parichehr, Zare Shahrokh, Razeghian-Jahromi Iman, Jalli Reza, Hamzavai Marzieh, Mehrabani Golshid, Zamiri Barbad, Karimi-Busheri Feridoun
Stem Cell Technology Research Center, Shiraz University of Medical Sciences Shiraz, Iran.
Burn and Wound Healing Research Center, Shiraz University of Medical Sciences Shiraz, Iran.
Am J Stem Cells. 2024 Apr 25;13(2):75-86. doi: 10.62347/UAFC3719. eCollection 2024.
Dental pulp stem cells (DPSCs) were shown to play an important role in regenerative medicine including reconstruction of various bone lesions. This study determined the impact of acemannan, an extracted product from , on proliferation of DPSCs and healing of mandibular defects in rabbits.
DPSCs were isolated and characterized. The growth kinetics of cells exposed to acemannan (8 mg/mL) and Hank's balanced salt solution (HBSS) were compared . Fifteen male rabbits were divided into 3 groups. Five animals were left as control group without any therapeutic intervention. Five rabbits were considered as experimental group 1 and received 20 µL of a cell suspension containing 10 DPSCs in the bone defect. Another 5 rabbits were regarded as experimental group 2 and were injected in the bone defect with 20 µL of a cell suspension containing 10 DPSCs treated with acemannan for 24 h. After 60 days, the animals were assessed by radiography and histologically.
The mesenchymal properties of DPSCs were confirmed. Population doubling time (PDT) of DPSCs treated with acemannan (29.8 h) was significantly shorter than cells were just exposed to HBSS (45.9 h). DPSCs together with acemannan could significantly accelerate the healing process and osteogenesis in mandibular defects.
As DPSCS showed an increased proliferation when treated with acemannan and accelerated the healing process in mandibular defects, these findings can open a new avenue in dentistry regenerative medicine when remedies of bone defects are targeted.
牙髓干细胞(DPSCs)已被证明在再生医学中发挥重要作用,包括各种骨损伤的修复。本研究确定了从 中提取的乙酰甘露聚糖对DPSCs增殖及兔下颌骨缺损愈合的影响。
分离并鉴定DPSCs。比较暴露于乙酰甘露聚糖(8 mg/mL)和汉克平衡盐溶液(HBSS)的细胞的生长动力学。15只雄性兔分为3组。5只动物作为对照组,不进行任何治疗干预。5只兔被视为实验组1,在骨缺损处接受20 μL含10个DPSCs的细胞悬液。另外5只兔被视为实验组2,在骨缺损处注射20 μL含10个经乙酰甘露聚糖处理24小时的DPSCs的细胞悬液。60天后,通过影像学和组织学对动物进行评估。
证实了DPSCs的间充质特性。用乙酰甘露聚糖处理的DPSCs的群体倍增时间(PDT)(29.8小时)明显短于仅暴露于HBSS的细胞(45.9小时)。DPSCs与乙酰甘露聚糖一起可显著加速下颌骨缺损的愈合过程和成骨作用。
由于DPSCs在用乙酰甘露聚糖处理时增殖增加,并加速了下颌骨缺损的愈合过程,当针对骨缺损的治疗时,这些发现可为牙科再生医学开辟一条新途径。