Blocking GATA6 Alleviates Pyroptosis and Inhibits Abdominal Wall Endometriosis Lesion Growth Through Inactivating the PI3K/AKT Pathway.

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiufang Du, Hongjie Yang, Xiaobei Kang, Changna Fu, Tao Yang
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引用次数: 0

Abstract

Endometriosis is a benign gynecological disorder characterized by the abnormal presence of endometrium-like cells, referred to as ectopic tissue, located outside the uterine cavity. Beyond the abnormal proliferation of endometrium-like tissues within and beyond the pelvic cavity, compelling scientific evidence underscores the crucial involvement of the NOD-like receptor NLRP3 inflammasome and pyroptosis in the pathogenesis of EMS. Our investigation has revealed a striking upregulation of the endogenous protein GATA-binding protein 6 (GATA6) in abdominal wall EMS. Notably, the knockdown of GATA6 significantly impaired the viability and migratory potential of primary ectopic endometrial stromal cells (EESCs) while also inhibiting crucial markers of pyroptosis, such as NLRP3, the gasdermin D N-terminal fragment (GSDMD-N), and reactive oxygen species (ROS) levels within these cells. Delving deeper into the underlying mechanisms, we discovered that suppressing GATA6 mitigated the activation of the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT) signaling pathway in EESCs. The administration of 740 Y-P, an agonist of the PI3K/AKT pathway, mitigated the inhibitive actions of GATA6 knockdown on EESCs' growth, migration, and pyroptosis, highlighting the intricate crosstalk between GATA6 and this intricate signaling cascade. In vivo experiments corroborated these findings, demonstrating that reduced GATA6 expression effectively restrained the growth of endometrial lesions and concurrently suppressed pyroptosis, accompanied by a dampening of PI3K/AKT signaling within these lesions. In summary, our study underscores the pivotal role of GATA6 in modulating the growth and pyroptosis of abdominal wall EMS through its regulation of the PI3K/AKT signaling pathway. Silencing GATA6 emerges as a promising approach to alleviate pyroptosis and potentially offers a novel therapeutic angle for managing abdominal wall EMS.

阻断 GATA6 可通过抑制 PI3K/AKT 通路缓解脓毒症并抑制腹壁子宫内膜异位症病灶生长
子宫内膜异位症是一种良性妇科疾病,其特征是位于子宫腔外的子宫内膜样细胞(被称为异位组织)的异常存在。除了子宫内膜样组织在盆腔内外的异常增殖外,令人信服的科学证据还强调了 NOD 样受体 NLRP3 炎性体和嗜热症在 EMS 发病机制中的关键作用。我们的研究发现,在腹壁 EMS 中,内源性蛋白 GATA 结合蛋白 6(GATA6)出现了惊人的上调。值得注意的是,敲除 GATA6 会显著降低原发性异位子宫内膜基质细胞(EESCs)的活力和迁移潜力,同时也会抑制这些细胞内的 NLRP3、gasdermin D N-terminal fragment(GSDMD-N)等重要化脓标志物以及活性氧(ROS)水平。深入探究其潜在机制,我们发现抑制 GATA6 可减轻 EESCs 中磷脂酰肌醇 3- 激酶(PI3K)/蛋白激酶 B(AKT)信号通路的激活。PI3K/AKT 通路的激动剂 740 Y-P 可减轻 GATA6 基因敲除对 EESCs 生长、迁移和热昏迷的抑制作用,这突显了 GATA6 与这一错综复杂的信号级联之间错综复杂的相互影响。体内实验证实了这些发现,证明减少 GATA6 的表达有效抑制了子宫内膜病变的生长,同时抑制了脓毒症,并抑制了这些病变中的 PI3K/AKT 信号传导。总之,我们的研究强调了 GATA6 通过调控 PI3K/AKT 信号通路在调节腹壁 EMS 生长和脓毒症中的关键作用。抑制 GATA6 是一种很有前景的方法,可减轻脓毒症,并有可能为治疗腹壁 EMS 提供一个新的治疗角度。
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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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