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单链DNA结合蛋白SSB1参与唾液腺辐射损伤修复的表达。

The single-strand DNA-binding protein SSB1 is involved in the expression of salivary gland radiation injury repair.

作者信息

Wang Xian, Wang Yuetong, Zeng Xianglin, Lu Haoyu, Mo Dongqin, Li Yuetao, Liu Zhiqing, Huang Yude, Yu Kun, Wang Daiyou

机构信息

College & Hospital of Stomatology, Guangxi Medical University, Nanning, Guangxi, China.

Guangxi Key Laboratory of Oral and Maxillofacial Rehabilitation and Reconstruction, Nanning, Guangxi, China.

出版信息

Front Pharmacol. 2024 Oct 15;15:1471996. doi: 10.3389/fphar.2024.1471996. eCollection 2024.

DOI:10.3389/fphar.2024.1471996
PMID:39474611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11518712/
Abstract

OBJECTIVES

Single-strand DNA-binding protein 1 (SSB1) plays a crucial role in the cellular response to DNA damage. This study aimed to explore the expression and regulation of SSB1 in normal rat salivary gland tissues and tissues following radiation, with a specific emphasis on its involvement in the repair of salivary gland injury.

METHODS

A total of 45 adult SD rats were randomly assigned to one control group or eight experimental groups. In the control group, five rats were euthanized without irradiation, and their parotid gland tissues were collected for analysis. The experimental groups received a dose of 6 Gy of radiation targeting the head and neck region; subsequently, five rats from each group were euthanized hly to collect parotid gland tissue samples, resulting in a total of eight experimental groups. The expression levels of SSB1, γ-H2AX, and PARP1 in the parotid gland tissues were assessed via immunohistochemistry, while changes in SSB1 gene expression were quantified via RT-qPCR.

RESULTS

No significant morphological differences were observed between the two groups following HE staining. In the immunohistochemistry (IHC) analysis, notable tissue-specific variation in SSB1 expression was identified, with higher levels detected in the ducts than in the acini and connective tissue. The expression of SSB1 gene initially increased post-radiation before subsequently decreasing, ultimately returning to baseline levels, as corroborated by the RT-qPCR results. In contrast, γ-H2AX and PARP1 exhibited minimal expression in the control group; however, their expression peaked at 1 h in the experimental group before gradually declining to levels comparable to those of the control group.

CONCLUSION

Radiation induces time-dependent upregulation of SSB1 expression in rat salivary glands, indicating that SSB1 may play a role in radiation-induced repair processes.

摘要

目的

单链DNA结合蛋白1(SSB1)在细胞对DNA损伤的反应中起关键作用。本研究旨在探讨SSB1在正常大鼠唾液腺组织及辐射后组织中的表达与调控,特别关注其在唾液腺损伤修复中的作用。

方法

将45只成年SD大鼠随机分为1个对照组和8个实验组。对照组5只大鼠未经照射即安乐死,收集其腮腺组织进行分析。实验组接受针对头颈部区域的6 Gy辐射剂量;随后,每组5只大鼠分别在不同时间点安乐死以收集腮腺组织样本,共形成8个实验组。通过免疫组织化学评估腮腺组织中SSB1、γ-H2AX和PARP1的表达水平,同时通过RT-qPCR定量SSB1基因表达的变化。

结果

HE染色后两组间未观察到明显形态学差异。在免疫组织化学(IHC)分析中,发现SSB1表达存在显著的组织特异性差异,导管中的表达水平高于腺泡和结缔组织。RT-qPCR结果证实,SSB1基因表达在辐射后最初升高,随后下降,最终恢复到基线水平。相比之下,γ-H2AX和PARP1在对照组中表达极少;然而,它们在实验组中的表达在1小时达到峰值,随后逐渐下降至与对照组相当的水平。

结论

辐射诱导大鼠唾液腺中SSB1表达呈时间依赖性上调,表明SSB1可能在辐射诱导的修复过程中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/f7fa4914317a/fphar-15-1471996-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/702be044a3bf/fphar-15-1471996-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/4351a53968df/fphar-15-1471996-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/2971b26ff518/fphar-15-1471996-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/a75fd4dccab2/fphar-15-1471996-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/f7fa4914317a/fphar-15-1471996-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/702be044a3bf/fphar-15-1471996-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/4351a53968df/fphar-15-1471996-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/2971b26ff518/fphar-15-1471996-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/a75fd4dccab2/fphar-15-1471996-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0546/11518712/f7fa4914317a/fphar-15-1471996-g005.jpg

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