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下调 Sonic hedgehog 信号诱导生殖器疣中的 G2 期阻滞。

Downregulation of Sonic hedgehog signaling induces G2-arrest in genital warts.

机构信息

Department of Dermatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Anaesthesiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Skin Res Technol. 2023 Jan;29(1):e13265. doi: 10.1111/srt.13265.

Abstract

BACKGROUND

Human papillomavirus (HPV) infected keratinocyte dysfunction results in the formation of genital warts, and the specific role of Sonic hedgehog (SHh) signaling in genital warts remains elusive. Thus, this study aimed to identify the correlation between wart formation and SHh signaling.

MATERIALS AND METHODS

In this study, nine male patients with genital warts were recruited, and the expression of SHh and its downstream signal molecules Patched-1 and GLI family zinc finger 1 (Ptch1 and Gli1) was detected. Moreover, G2-phase cells in the collected genital warts samples were assessed with normal foreskin samples as a comparison. HPV6/11 were detected via in situ hybridization (ISH), and SHh expression of the corresponding paraffin sections was determined via immunohistochemical staining (IHC). In addition, an in vitro down-regulated SHh model was constructed by siRNA transfection of the HaCaT cell line, and the cell cycle was detected at 36 h by flow cytometry with propidium iodide staining.

RESULTS

SHh, Ptch1, and Gli1 in warts were significantly downregulated in the condyloma acuminatum (CA) group compared to the normal foreskin group. G2-phase cells in the middle section of the spinous layer of CA wart tissues were significantly increased. Moreover, the expression of HPV-DNA was amplified and negatively correlated with SHh activity in CA wart tissues. Lastly, the downregulation of SHh-induced G2 arrest in vitro.

CONCLUSIONS

The downregulation of the SHh signaling promotes HPV replication and the formation of warts by inducing G2/M arrest in the keratinocytes of CA.

摘要

背景

人乳头瘤病毒(HPV)感染的角质形成细胞功能障碍导致生殖器疣的形成,而 Sonic hedgehog(SHh)信号在生殖器疣中的具体作用仍不清楚。因此,本研究旨在确定疣形成与 SHh 信号之间的相关性。

材料和方法

在这项研究中,招募了 9 名男性生殖器疣患者,并检测了 SHh 及其下游信号分子 Patched-1 和 Gli 家族锌指蛋白 1(Ptch1 和 Gli1)的表达。此外,还评估了收集的生殖器疣样本中的 G2 期细胞与正常包皮样本进行比较。通过原位杂交(ISH)检测 HPV6/11,并用免疫组织化学染色(IHC)检测相应石蜡切片中的 SHh 表达。此外,通过 siRNA 转染 HaCaT 细胞系构建了 SHh 下调的体外模型,并通过碘化丙啶染色的流式细胞术在 36 小时检测细胞周期。

结果

与正常包皮组相比,尖锐湿疣(CA)组的 SHh、Ptch1 和 Gli1 在疣中明显下调。CA 疣组织棘层中层的 G2 期细胞明显增加。此外,CA 疣组织中 HPV-DNA 的表达被扩增,与 SHh 活性呈负相关。最后,体外下调 SHh 诱导的 G2 期阻滞。

结论

SHh 信号的下调通过诱导 CA 角质形成细胞中的 G2/M 阻滞,促进 HPV 复制和疣的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c544/9838784/e814e104baad/SRT-29-e13265-g001.jpg

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