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储存条件对牙周膜细胞克隆形成能力的影响:对牙再植的启示

The influence of storage conditions on the clonogenic capacity of periodontal ligament cells: implications for tooth replantation.

作者信息

Lekic P C, Kenny D J, Barrett E J

机构信息

Faculty of Dentistry, University of Manitoba, Winnipeg, Canada.

出版信息

Int Endod J. 1998 Mar;31(2):137-40. doi: 10.1046/j.1365-2591.1998.00138.x.

Abstract

Viable periodontal ligament (PL) cells are required for PL healing of avulsed teeth following replantation. If immediate replantation cannot be accomplished, the ability of PL progenitor cells to reproduce (clonogenic capacity) and recolonize the wound may be extended by prevention of desiccation and storage in physiological media. This investigation examined the effects of storage in saliva, milk, Hank's balanced salt solution (HBSS) and Eagle's medium (alpha MEM) on the clonogenic capacity of human PL progenitor cells at 30 and 60 min extra-alveolar time. Twenty erupted human premolar teeth extracted as atraumatically as possible for orthodontic purposes were used in the present study. Fifteen premolars were placed immediately in freshly collected autologous saliva at room temperature, (+ 23 degrees C) for 15 min. These 15 premolars were next divided into three groups of five and stored in either saliva, milk or HBSS at + 4 degrees C in plastic cups surrounded by ice. The remaining five teeth served as positive controls and were immediately placed in alpha MEM at + 4 degrees C. PL tissue was scraped from one-half of the root surface with a scalpel at 30 and 60 min total extra-alveolar duration. Cells were released from the tissue sample with a 30 min enzymatic digestion procedure and the cells from the tissue samples analyzed for clonogenic capacity. There was a reduction in clonogenic capacity with time for all protocols. Periodontal ligament cells stored in alpha MEM showed the least reduction between 30 and 60 min and the greatest reduction was observed for PL cells stored in saliva. The difference in clonogenic capacity following transfer from saliva to milk or HBSS was not significant at 30 min. At 60 min, cells transferred from saliva to HBSS had a statistically higher percentage of clonogenic cells than those transferred to milk (5.9% vs. 3.5%; P < 0.05). We conclude that immediate storage of avulsed teeth in autologous saliva, followed by transfer to chilled milk, preserves the presence of sufficient progenitor cells in the PL to warrant replantation and the possibility of PL healing at 60 min extra-alveolar duration.

摘要

再植后,存活的牙周膜(PL)细胞是牙齿撕脱伤后牙周膜愈合所必需的。如果无法立即进行再植,通过防止干燥并将其保存在生理介质中,牙周膜祖细胞的繁殖能力(克隆形成能力)和在伤口处重新定植的能力可能会得到延长。本研究调查了在30分钟和60分钟的牙槽外时间内,保存在唾液、牛奶、汉克平衡盐溶液(HBSS)和伊格尔培养基(α-MEM)中对人牙周膜祖细胞克隆形成能力的影响。本研究使用了20颗因正畸目的尽可能无创拔除的萌出人类前磨牙。15颗前磨牙立即置于室温(+23℃)下新鲜采集的自体唾液中15分钟。接下来,将这15颗前磨牙分成三组,每组五颗,分别保存在唾液、牛奶或HBSS中,置于+4℃的塑料杯中并用冰包围。其余五颗牙齿作为阳性对照,立即置于+4℃的α-MEM中。在牙槽外总时长30分钟和60分钟时,用手术刀从牙根表面的一半刮下牙周膜组织。通过30分钟的酶消化程序从组织样本中释放细胞,并分析组织样本中的细胞的克隆形成能力。所有方案的克隆形成能力均随时间下降。保存在α-MEM中的牙周膜细胞在30分钟至60分钟之间减少最少,而保存在唾液中的牙周膜细胞减少最多。在30分钟时,从唾液转移到牛奶或HBSS后克隆形成能力的差异不显著。在60分钟时,从唾液转移到HBSS的细胞中具有克隆形成能力的细胞百分比在统计学上高于转移到牛奶中的细胞(5.9%对3.5%;P<0.05)。我们得出结论,将撕脱的牙齿立即保存在自体唾液中,然后转移到冷藏牛奶中,可以使牙周膜中保留足够的祖细胞,从而保证在牙槽外时长60分钟时进行再植以及牙周膜愈合的可能性。

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