• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

博来霉素吸入后雄性和雌性小鼠肺唾液酸酶的变化。

Changes in lung sialidases in male and female mice after bleomycin aspiration.

机构信息

Texas A&M University, College Station, Texas.

出版信息

Exp Lung Res. 2022 Nov-Dec;48(9-10):291-304. doi: 10.1080/01902148.2022.2144548. Epub 2022 Nov 16.

DOI:10.1080/01902148.2022.2144548
PMID:36382835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10084762/
Abstract

Sialidases, also called neuraminidases, are enzymes that cleave terminal sialic acids from glycoconjugates. In humans and mice, lung fibrosis is associated with desialylation of glycoconjugates and upregulation of sialidases. There are four mammalian sialidases, and it is unclear when the four mammalian sialidases are elevated over the course of inflammatory and fibrotic responses, whether tissue resident and inflammatory cells express different sialidases, and if sialidases are differentially expressed in male and females. To determine the time course of sialidase expression and the identity of sialidase expressing cells, we used the bleomycin model of pulmonary fibrosis in mice to examine levels of sialidases during inflammation (days 3 - 10) and fibrosis (days 10 - 21). Bleomycin aspiration increased sialidase NEU1 at days 14 and 21 in male mice and day 10 in female mice. NEU2 levels increased at day 7 in male and day 10 in female mice. NEU3 appears to have a biphasic response in male mice with increased levels at day 7 and then at days 14 and 21, whereas in female mice NEU3 levels increased over 21 days. In control mice, the sialidases were mainly expressed by EpCAM positive epithelial cells, but after bleomycin, epithelial cells, CD45 positive immune cells, and alveolar cells expressed NEU1, NEU2, and NEU3. Sialidase expression was higher in male compared to female mice. There was little expression of NEU4 in murine lung tissue. These results suggest that sialidases are dynamically expressed following bleomycin, that sialidases are differentially expressed in male and females, and that of the four sialidases only NEU3 upregulation is associated with fibrosis in both male and female mice.

摘要

唾液酸酶,也称为神经氨酸酶,是能够从糖缀合物上切割末端唾液酸的酶。在人和小鼠中,肺纤维化与糖缀合物的去唾液酸化和唾液酸酶的上调有关。哺乳动物中有四种唾液酸酶,目前尚不清楚在炎症和纤维化反应过程中,这四种哺乳动物唾液酸酶何时升高,组织驻留细胞和炎症细胞是否表达不同的唾液酸酶,以及唾液酸酶在男性和女性中是否存在差异表达。为了确定唾液酸酶表达的时间进程以及表达唾液酸酶的细胞的身份,我们使用博来霉素诱导的肺纤维化模型在小鼠中检查了炎症(第 3-10 天)和纤维化(第 10-21 天)期间的唾液酸酶水平。博来霉素吸入增加了雄性小鼠第 14 天和第 21 天以及雌性小鼠第 10 天的唾液酸酶 NEU1 水平。NEU2 水平在雄性小鼠第 7 天和雌性小鼠第 10 天增加。NEU3 在雄性小鼠中似乎呈双相反应,在第 7 天和第 14 天和第 21 天水平增加,而在雌性小鼠中,NEU3 水平在 21 天内增加。在对照小鼠中,唾液酸酶主要由 EpCAM 阳性上皮细胞表达,但在用博来霉素处理后,上皮细胞、CD45 阳性免疫细胞和肺泡细胞表达了 NEU1、NEU2 和 NEU3。与雌性小鼠相比,雄性小鼠中唾液酸酶的表达更高。在小鼠肺组织中很少表达 NEU4。这些结果表明,博来霉素后唾液酸酶会动态表达,唾液酸酶在雄性和雌性中存在差异表达,并且在这四种唾液酸酶中,只有 NEU3 的上调与雄性和雌性小鼠的纤维化都有关。

相似文献

1
Changes in lung sialidases in male and female mice after bleomycin aspiration.博来霉素吸入后雄性和雌性小鼠肺唾液酸酶的变化。
Exp Lung Res. 2022 Nov-Dec;48(9-10):291-304. doi: 10.1080/01902148.2022.2144548. Epub 2022 Nov 16.
2
Attenuated pulmonary fibrosis in sialidase-3 knockout () mice.唾液酸酶 3 基因敲除()小鼠的肺纤维化减弱。
Am J Physiol Lung Cell Mol Physiol. 2020 Jan 1;318(1):L165-L179. doi: 10.1152/ajplung.00275.2019. Epub 2019 Oct 16.
3
The sialidase NEU3 promotes pulmonary fibrosis in mice.唾液酸酶 NEU3 促进小鼠肺纤维化。
Respir Res. 2022 Aug 23;23(1):215. doi: 10.1186/s12931-022-02146-y.
4
Inhibiting Sialidase-Induced TGF-1 Activation Attenuates Pulmonary Fibrosis in Mice.抑制唾液酸酶诱导的 TGF-β1 激活可减轻小鼠肺纤维化。
J Pharmacol Exp Ther. 2021 Jan;376(1):106-117. doi: 10.1124/jpet.120.000258. Epub 2020 Nov 3.
5
Inhibitors of the Sialidase NEU3 as Potential Therapeutics for Fibrosis.唾液酸酶 NEU3 的抑制剂作为纤维化的潜在治疗方法。
Int J Mol Sci. 2022 Dec 23;24(1):239. doi: 10.3390/ijms24010239.
6
The extracellular sialidase NEU3 primes neutrophils.细胞外唾液酸酶 NEU3 可激活中性粒细胞。
J Leukoc Biol. 2022 Dec;112(6):1399-1411. doi: 10.1002/JLB.3A0422-217RR. Epub 2022 Jul 28.
7
Sialidase inhibitors attenuate pulmonary fibrosis in a mouse model.唾液酸酶抑制剂可减轻小鼠肺纤维化模型中的肺纤维化。
Sci Rep. 2017 Nov 8;7(1):15069. doi: 10.1038/s41598-017-15198-8.
8
Sialidase NEU3 and its pathological significance.唾液酸酶 NEU3 及其病理意义。
Glycoconj J. 2022 Oct;39(5):677-683. doi: 10.1007/s10719-022-10067-7. Epub 2022 Jun 8.
9
Novel Nile tilapia Neu1 sialidases: Molecular cloning and biochemical characterization of the sialidases Neu1a and Neu1b.新型尼罗罗非鱼 Neu1 唾液酸酶:Neu1a 和 Neu1b 唾液酸酶的分子克隆和生化特性分析。
Gene. 2020 Jun 5;742:144538. doi: 10.1016/j.gene.2020.144538. Epub 2020 Mar 14.
10
Cellular translocation and secretion of sialidases.唾液酸酶的细胞转位和分泌。
J Biol Chem. 2024 Sep;300(9):107671. doi: 10.1016/j.jbc.2024.107671. Epub 2024 Aug 14.

引用本文的文献

1
Genomic regions associated with bovine respiratory disease in pacific northwest Holstein cattle.与太平洋西北地区荷斯坦奶牛牛呼吸道疾病相关的基因组区域。
Front Vet Sci. 2025 Jul 31;12:1637087. doi: 10.3389/fvets.2025.1637087. eCollection 2025.
2
Inhibition of CCl4-induced liver inflammation and fibrosis by a NEU3 inhibitor.NEU3 抑制剂抑制 CCl4 诱导的肝炎症和纤维化。
PLoS One. 2024 Nov 21;19(11):e0308060. doi: 10.1371/journal.pone.0308060. eCollection 2024.
3
The role of sialidase Neu1 in respiratory diseases.神经氨酸酶 Neu1 在呼吸疾病中的作用。

本文引用的文献

1
The sialidase NEU3 promotes pulmonary fibrosis in mice.唾液酸酶 NEU3 促进小鼠肺纤维化。
Respir Res. 2022 Aug 23;23(1):215. doi: 10.1186/s12931-022-02146-y.
2
Altered sialidase expression in human myeloid cells undergoing apoptosis and differentiation.人髓样细胞凋亡和分化时唾液酸酶表达的改变。
Sci Rep. 2022 Aug 19;12(1):14173. doi: 10.1038/s41598-022-18448-6.
3
Time and phenotype-dependent transcriptome analysis in AAV-TGFβ1 and Bleomycin-induced lung fibrosis models.时间和表型依赖性转录组分析在 AAV-TGFβ1 和博来霉素诱导的肺纤维化模型中。
Respir Res. 2024 Mar 19;25(1):134. doi: 10.1186/s12931-024-02763-9.
4
Inhibitors of the Sialidase NEU3 as Potential Therapeutics for Fibrosis.唾液酸酶 NEU3 的抑制剂作为纤维化的潜在治疗方法。
Int J Mol Sci. 2022 Dec 23;24(1):239. doi: 10.3390/ijms24010239.
Sci Rep. 2022 Jul 16;12(1):12190. doi: 10.1038/s41598-022-16344-7.
4
Sialidase NEU3 and its pathological significance.唾液酸酶 NEU3 及其病理意义。
Glycoconj J. 2022 Oct;39(5):677-683. doi: 10.1007/s10719-022-10067-7. Epub 2022 Jun 8.
5
Neuraminidase 1 deficiency attenuates cardiac dysfunction, oxidative stress, fibrosis, inflammatory via AMPK-SIRT3 pathway in diabetic cardiomyopathy mice.神经氨酸酶 1 缺乏通过 AMPK-SIRT3 通路减轻糖尿病心肌病小鼠的心功能障碍、氧化应激、纤维化和炎症。
Int J Biol Sci. 2022 Jan 1;18(2):826-840. doi: 10.7150/ijbs.65938. eCollection 2022.
6
Neuraminidase 1 is a driver of experimental cardiac hypertrophy.神经氨酸酶 1 是实验性心肌肥厚的驱动因素。
Eur Heart J. 2021 Sep 21;42(36):3770-3782. doi: 10.1093/eurheartj/ehab347.
7
Targeting Alveolar Repair in Idiopathic Pulmonary Fibrosis.靶向特发性肺纤维化的肺泡修复。
Am J Respir Cell Mol Biol. 2021 Oct;65(4):347-365. doi: 10.1165/rcmb.2020-0476TR.
8
Sex-Related Differences in Murine Models of Chemically Induced Pulmonary Fibrosis.化学诱导性肺纤维化的小鼠模型中的性别差异。
Int J Mol Sci. 2021 May 31;22(11):5909. doi: 10.3390/ijms22115909.
9
Neuraminidases 1 and 3 Trigger Atherosclerosis by Desialylating Low-Density Lipoproteins and Increasing Their Uptake by Macrophages.神经氨酸酶 1 和 3 通过脱唾液酸化低密度脂蛋白并增加其被巨噬细胞摄取来引发动脉粥样硬化。
J Am Heart Assoc. 2021 Feb 16;10(4):e018756. doi: 10.1161/JAHA.120.018756. Epub 2021 Feb 6.
10
Serum Amyloid P inhibits single stranded RNA-induced lung inflammation, lung damage, and cytokine storm in mice.血清淀粉样蛋白 P 抑制单链 RNA 诱导的小鼠肺部炎症、肺损伤和细胞因子风暴。
PLoS One. 2021 Jan 22;16(1):e0245924. doi: 10.1371/journal.pone.0245924. eCollection 2021.