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小鼠舌黏膜在每日分次放疗期间的组织动力学

Tissue kinetics in mouse tongue mucosa during daily fractionated radiotherapy.

作者信息

Dörr W, Emmendörfer H, Weber-Frisch M

机构信息

Klinik und Poliklinik für Strahlentherapie, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.

出版信息

Cell Prolif. 1996 Sep;29(9):495-504. doi: 10.1111/j.1365-2184.1996.tb00992.x.

Abstract

The purpose of the present investigation was to quantify cell flux between the distinct layers of the epithelial lining of the ventral surface of mouse tongue during daily fractionated radiotherapy. A fraction of DNA-synthesizing cells in control epithelium, or at various days through a course of daily fractionated radiotherapy with 3 or 4 Gy per day, was labelled with [3H]dT or BrdUrd, respectively. The labelling indices (LI) in the different epithelial layers were defined histologically after autoradiography, or immunohistochemistry, at intervals between 1 and 10 days after label administration. In tongue epithelium of untreated mice, the minimum residence time of cells in the germinal layer is 2-3 days. Migration through the functional layers requires an additional 2-3 days before labelled cells are observed in the most superficial layer of nucleated cells. A plateau in LI is observed for several days post-labelling in control epithelium, indicating an equilibrium between loss and proliferation of labelled cells. During fractionated radiotherapy, the minimum time from division to occurrence of labelled cells in the stratum lucidum is less than 2 days, and hence significantly shorter than in control epithelium. In contrast to untreated epithelium, no plateau in the germinal layer LI is seen, indicating that frequently both labelled daughters from dividing labelled cells are being lost from this compartment. In conclusion, the present data support a recently described model of radiation-induced accelerated repopulation in squamous epithelia, which postulates that the majority of damaged cells undergoes abortive' divisions resulting in two differentiating daughters.

摘要

本研究的目的是量化小鼠舌腹侧上皮衬里不同层之间在每日分次放疗期间的细胞通量。分别用[³H]胸苷或溴脱氧尿苷标记对照上皮中或在每天3或4 Gy的每日分次放疗过程中不同天数的一部分DNA合成细胞。在给予标记物后1至10天的间隔时间,通过放射自显影或免疫组织化学进行组织学定义不同上皮层中的标记指数(LI)。在未处理小鼠的舌上皮中,生发层中细胞的最短停留时间为2 - 3天。穿过功能层迁移还需要额外的2 - 3天,之后才能在有核细胞的最表层观察到标记细胞。在对照上皮中,标记后几天观察到LI达到平台期,表明标记细胞损失与增殖之间达到平衡。在分次放疗期间,从分裂到在透明层出现标记细胞的最短时间小于2天,因此明显短于对照上皮。与未处理的上皮不同,生发层LI未见平台期,这表明分裂的标记细胞产生的两个标记子代经常从该区域丢失。总之,本数据支持最近描述的鳞状上皮辐射诱导加速再增殖模型,该模型假定大多数受损细胞进行“流产”分裂,产生两个分化的子代。

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