Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

3.8K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
3.8K
Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

2.6K
Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
2.6K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

3.6K
The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
3.6K
Mechanism of Angiogenesis01:10

Mechanism of Angiogenesis

5.5K
Blood vessel formation starts early during embryonic development, around day 7. In the extraembryonic yolk sac, mesodermal precursor cells called hemangioblast proliferate and differentiate into angioblast. Angioblasts express vascular endothelial growth factor receptor 2 or VEGFR2, which binds VEGF-A, a proangiogenic factor, guiding blood vessel formation. VEGF signaling promotes angioblasts to form a blood island in the developing embryo. Angioblasts further differentiate, giving rise to...
5.5K
Notch Signaling Pathway03:14

Notch Signaling Pathway

4.3K
The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
4.3K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

RNAlater-compatible protocol for nuclei isolation from radical prostatectomy prostate cancer resections, enabling single-nucleus resolution RNA-seq.

Scientific reports·2026
Same author

GFI1B mutations define an emerging form of inherited thrombocytopenia: insights from a case report and literature review.

Annals of hematology·2026
Same author

Analysis of the Occurrence of <i>PIK3CA</i> Gene Mutation in Children with Lymphatic Malformation-Single Center Study.

Children (Basel, Switzerland)·2025
Same author

Unruptured Intracranial Aneurysm Risk Scores Underperform in Predicting Subsequent Rupture: A Retrospective Single-Center Study.

Neurology international·2025
Same author

Molecular Landscape of Prostate Cancer Across Age Groups: Impact on Prognosis and Treatment Outcomes.

International journal of molecular sciences·2025
Same author

IGH::IL3-Rearranged B-Cell Precursor Acute Lymphoblastic Leukemia With Hypereosinophilia in a Child With a Novel PAX5 Germline Variant.

Genes, chromosomes & cancer·2025

相关实验视频

Updated: Jul 6, 2025

A Patient-Derived Xenograft Model for Venous Malformation
06:51

A Patient-Derived Xenograft Model for Venous Malformation

Published on: June 15, 2020

5.3K

mTOR通路基质在血管形中呈现高活性,并且随着年龄的增长而显著减少.

Jakub Kopeć1, Elżbieta Sałacińska-Łoś1, Magdalena Orzechowska2

  • 1Pediatric Surgery and Oncology Department, Medical University of Łódź, 90-419 Lodz, Poland.

Diagnostics (Basel, Switzerland)
|January 11, 2024
PubMed
概括

血管形显示了拉巴胺素 (mTOR) 途径基质激活的哺乳动物标高于健康组织. 这表明mTOR.

关键词:
淋巴细胞形的错误形成.在mTOROR中使用.这种药物是拉帕米辛 (Rapamycin).这是西洛利斯 (sirolimus).血管异常的发生.维纳斯的缺陷形成

更多相关视频

An Ex Vivo Choroid Sprouting Assay of Ocular Microvascular Angiogenesis
06:10

An Ex Vivo Choroid Sprouting Assay of Ocular Microvascular Angiogenesis

Published on: August 6, 2020

5.6K
Development of a Murine Model for Femoral Artery Anastomotic Stenosis
05:42

Development of a Murine Model for Femoral Artery Anastomotic Stenosis

Published on: April 18, 2025

154

相关实验视频

Last Updated: Jul 6, 2025

A Patient-Derived Xenograft Model for Venous Malformation
06:51

A Patient-Derived Xenograft Model for Venous Malformation

Published on: June 15, 2020

5.3K
An Ex Vivo Choroid Sprouting Assay of Ocular Microvascular Angiogenesis
06:10

An Ex Vivo Choroid Sprouting Assay of Ocular Microvascular Angiogenesis

Published on: August 6, 2020

5.6K
Development of a Murine Model for Femoral Artery Anastomotic Stenosis
05:42

Development of a Murine Model for Femoral Artery Anastomotic Stenosis

Published on: April 18, 2025

154

科学领域:

  • 血管生物学和细胞信号传递.
  • 皮肤病学和医学研究.

背景情况:

  • 血管异常导致患者患病率显著,并具有挑战性治疗.
  • 猛素 (mTOR) 途径的哺乳动物点与血管形的发展有关.
  • 在这些条件下,mTOR失调的具体机制尚不清楚.

研究的目的:

  • 为了研究拉巴胺素 (mTOR) 途径基质的关键哺乳动物标的激活状态.
  • 评估mTOR信号传导在血管异常病变发生中的作用.

主要方法:

  • 组织病理学分析来自82名患有各种血管形的患者和健康对照的组织样本.
  • 针对p70 S6 激酶,4EBP1和p-4EBP1.1进行免疫组织化学染色.
  • 使用R包 (FactoMineR,factoextra) 的统计分析.

主要成果:

  • 与健康组织相比,血管形表现出明显更高的mTOR基质激活.
  • 在有形的女性中,注意到p-4EBP1表达的升高.
  • 随着年龄的增长,mTOR基质表达减少.

结论:

  • 血管形中mTOR基质表达的增加支持其在异常血管发育中的作用.
  • 在mTOR信号的年龄依赖的变化表明年龄特定的治疗策略的潜力.
  • 了解mTOR通路激活为个性化医疗方法提供了潜在的治疗点.