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Iqgap3-Ras 轴在胃体的稳态和修复过程中驱动干细胞增殖。

Iqgap3-Ras axis drives stem cell proliferation in the stomach corpus during homoeostasis and repair.

机构信息

Cancer Science Institute of Singapore, National University of Singapore, Singapore.

Department of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.

出版信息

Gut. 2021 Oct;70(10):1833-1846. doi: 10.1136/gutjnl-2020-322779. Epub 2020 Dec 8.

Abstract

OBJECTIVE

Tissue stem cells are central regulators of organ homoeostasis. We looked for a protein that is exclusively expressed and functionally involved in stem cell activity in rapidly proliferating isthmus stem cells in the stomach corpus.

DESIGN

We uncovered the specific expression of Iqgap3 in proliferating isthmus stem cells through immunofluorescence and in situ hybridisation. We performed lineage tracing and transcriptomic analysis of Iqgap3 +isthmus stem cells with the mouse model. Depletion of Iqgap3 revealed its functional importance in maintenance and proliferation of stem cells. We further studied Iqgap3 expression and the associated gene expression changes during tissue repair after tamoxifen-induced damage. Immunohistochemistry revealed elevated expression of Iqgap3 in proliferating regions of gastric tumours from patient samples.

RESULTS

Iqgap3 is a highly specific marker of proliferating isthmus stem cells during homoeostasis. Iqgap3+isthmus stem cells give rise to major cell types of the corpus unit. Iqgap3 expression is essential for the maintenance of stem potential. The Ras pathway is a critical partner of Iqgap3 in promoting strong proliferation in isthmus stem cells. The robust induction of Iqgap3 expression following tissue damage indicates an active role for Iqgap3 in tissue regeneration.

CONCLUSION

IQGAP3 is a major regulator of stomach epithelial tissue homoeostasis and repair. The upregulation of IQGAP3 in gastric cancer suggests that IQGAP3 plays an important role in cancer cell proliferation.

摘要

目的

组织干细胞是器官同源平衡的核心调节者。我们寻找一种仅在胃体部快速增殖的峡部干细胞中表达并参与干细胞活性的功能蛋白。

设计

我们通过免疫荧光和原位杂交技术发现 IQGAP3 在增殖的峡部干细胞中特异性表达。我们使用小鼠模型对 IQGAP3+峡部干细胞进行谱系追踪和转录组分析。IQGAP3 的耗竭揭示了其在维持和增殖干细胞中的功能重要性。我们进一步研究了 IQGAP3 在他莫昔芬诱导损伤后组织修复过程中的表达及其相关基因表达变化。免疫组织化学显示,来自患者样本的胃肿瘤增殖区域中 IQGAP3 的表达升高。

结果

IQGAP3 是同源平衡过程中增殖的峡部干细胞的高度特异性标志物。IQGAP3+峡部干细胞产生胃单位的主要细胞类型。IQGAP3 表达对于维持干细胞潜能至关重要。Ras 通路是 IQGAP3 在促进峡部干细胞强烈增殖中的关键伙伴。组织损伤后 IQGAP3 表达的强烈诱导表明 IQGAP3 在组织再生中具有积极作用。

结论

IQGAP3 是胃上皮组织同源平衡和修复的主要调节剂。IQGAP3 在胃癌中的上调表明 IQGAP3 在癌细胞增殖中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae71/8458072/f85c26387536/gutjnl-2020-322779f01.jpg

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