Jove
Visualize
お問い合わせ

関連する概念動画

Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists

223
Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
223
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

253
Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
253
Receptor Downregulation in MVBs01:15

Receptor Downregulation in MVBs

2.1K
Multivesicular bodies (MVBs) are mature endosomes that sort ubiquitinated proteins and then fuse with lysosomes to degrade the sorted proteins. Epidermal growth factor (EGF) and its receptor (EGFR) form a complex that can be internalized through endocytosis, sorted into an MVB, and later degraded.
The EGFR can initiate signaling pathways that  lead to cell proliferation, migration, and differentiation. Overexpression of EGFR  stimulates cells to proliferate. Excessive  EGFR...
2.1K
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

251
Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
251
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

7.8K
The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
7.8K
JoVE
x logofacebook logolinkedin logoyoutube logo
JoVEについて
概要リーダーシップブログJoVEヘルプセンター
著者向け
出版プロセス編集委員会範囲と方針査読よくある質問投稿
図書館員向け
推薦の声購読アクセスリソース図書館諮問委員会よくある質問
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experimentsアーカイブ
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教員リソースセンター教員サイト
利用規約
プライバシーポリシー
ポリシー
  1. ホーム
  2. E3ユビキチンリガゼを標的にする:イディオパシー性肺線維症の治療における新しい境界
  1. ホーム
  2. E3ユビキチンリガゼを標的にする:イディオパシー性肺線維症の治療における新しい境界

関連する実験動画

Refined Murine Model of Idiopathic Pulmonary Fibrosis
07:51

Refined Murine Model of Idiopathic Pulmonary Fibrosis

Published on: June 17, 2025

287

E3ユビキチンリガゼを標的にする:イディオパシー性肺線維症の治療における新しい境界

Kun Zhang1, Hui Yuan1, Lin Shi1

  • 1Department of Pediatric Cardiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.

Frontiers in immunology
|September 3, 2025

PubMed で要約を見る

まとめ
この要約は機械生成です。

E3ユビキチンリガゼは細胞機能を調節する上で極めて重要です. このレビューは,肺線維症における彼らの役割を強調し,イディオパシー肺線維症 (IPF) の潜在的な治療標的を提供している.

キーワード:
E3ユビキチンリガゼエピテリア・メゼンキマ移行イディオパシー肺線維症プロフィブロティック・フィブロブラスト変換成長因子-β

さらに関連する動画

Unilateral Lung Volume Analysis Using Micro-CT for Enhanced Assessment of Pulmonary Fibrosis in Preclinical Models
03:38

Unilateral Lung Volume Analysis Using Micro-CT for Enhanced Assessment of Pulmonary Fibrosis in Preclinical Models

Published on: June 20, 2025

322
Evaluation of Substrate Ubiquitylation by E3 Ubiquitin-ligase in Mammalian Cell Lysates
09:47

Evaluation of Substrate Ubiquitylation by E3 Ubiquitin-ligase in Mammalian Cell Lysates

Published on: May 10, 2022

2.7K

関連する実験動画

Refined Murine Model of Idiopathic Pulmonary Fibrosis
07:51

Refined Murine Model of Idiopathic Pulmonary Fibrosis

Published on: June 17, 2025

287
Unilateral Lung Volume Analysis Using Micro-CT for Enhanced Assessment of Pulmonary Fibrosis in Preclinical Models
03:38

Unilateral Lung Volume Analysis Using Micro-CT for Enhanced Assessment of Pulmonary Fibrosis in Preclinical Models

Published on: June 20, 2025

322
Evaluation of Substrate Ubiquitylation by E3 Ubiquitin-ligase in Mammalian Cell Lysates
09:47

Evaluation of Substrate Ubiquitylation by E3 Ubiquitin-ligase in Mammalian Cell Lysates

Published on: May 10, 2022

2.7K

科学分野:

  • 生化学と分子生物学
  • 細胞生物学
  • 病理学について

背景:

  • ユビキチネーションは,真核細胞における重要な翻訳後の変化である.
  • ユビキチネーションの調節不良は,様々な生命を脅かす病気と関連しています.
  • E3ユビキチンリガゼは,ユビキチン- プロテアソームシステムとTGF-βシグナル伝達を通じてタンパク質ホメオスタシスの主要な調節剤である.

研究 の 目的:

  • 肺線維症におけるE3ユビキチンリガゼの調節メカニズムを探求する.
  • Idiopathic pulmonary fibrosis (IPF) の発症に関与する特定のE3リガスを特定する.
  • IPFの治療と診断のためのE3リガゼを標的とした治療の可能性を強調する.

主な方法:

  • E3ユビキチンリガゼと肺線維症に関する既存の研究の文献レビュー.
  • 細胞プロセスにおけるE3リガゼを含む規制経路の分析.
  • IPFの病原性に関連したE3リガスの識別とコンパイル.

主要な成果:

  • E3ユビキチン結合体は,肺線維症の病原性において重要な役割を果たします.
  • いくつかの特定のE3リガゼは,IPF開発の重要なプレイヤーとして特定されています.
  • これらの相互作用を理解すると 病気のメカニズムに洞察が得られます
  • 結論:

    • E3ユビキチンリガゼは,イディオパシー性肺線維症の有望な治療標的である.
    • E3リガースの機能に関するさらなる研究は,IPFの新たな診断および治療戦略につながる可能性があります.
    • ユビキチネーション経路をターゲットにすることで 繊維性肺疾患の治療に 新たな道が開かれます