lysophosphatidic 酸受体 3 (LPAR3) 通过信号传递调节眼睛表面化物运输
Ethan S Lindgren1, Rongshan Yan1, Yien-Ming Kuo1
1Department of Ophthalmology, University of California, San Francisco, USA.
lysophosphatidic 酸受体 (LPAR) 调节了膜的稳态. 激活LPAR3刺激化物分泌,这表明LPAR3激动剂可以治疗干眼疾病.
科学领域:
- 眼科医生 眼科 眼科
- 细胞生物学 细胞生物学
- 分子药理学分子药理学
背景情况:
- 干眼疾病包括眼膜平衡受损和眼睛表面损伤.
- lysophosphatidic 酸受体 (LPAR) 是G蛋白合受体,影响细胞信号传递和伤口愈合.
研究的目的:
- 为了研究LPARs在眼睛表面上皮质细胞中的表达和功能.
- 探索LPAR调制治疗干眼等眼睛表面疾病的潜力.
主要方法:
- 使用LPAR调节器在小鼠眼表面电位差异 (OSPD) 的功能测量.
- 在小鼠和人类的眼睛组织和眼腺体中对LPAR3进行免疫抑制.
- 研究LPAR诱导的人类角膜上皮细胞 (HCEC) 中的 (Ca2+) 信号传递.
主要成果:
- LPAR激动剂通过Ca2+激活的Cl-通道 (CaCCs) 刺激了眼睛表面的化物分泌.
- LPAR3在小鼠和人类的角膜和结膜表皮和眼腺体中得到表达.
- 在HCEC中LPAR和LPAR3的激活通过Gq/PLC通路增加了细胞内Ca2+.
结论:
- LPAR3存在于眼睛表面上皮质和眼腺.
- 激活LPAR3促进化物分泌,这是维持眼睛表面水分的关键功能.
- LPAR3激动剂对干眼疾病和其他眼表面疾病具有治疗潜力.
更多相关视频
08:54Monitoring Leucine-Rich Repeat Containing 8 Channel (LRRC8/VRAC) Activity Using Sensitized-Emission Förster Resonance Energy Transfer (SE-FRET)
Published on: August 9, 2024
13:40Live Cell Calcium Imaging Combined with siRNA Mediated Gene Silencing Identifies Ca2+ Leak Channels in the ER Membrane and their Regulatory Mechanisms
Published on: July 7, 2011
相关概念视频
IP3/DAG Signaling Pathway
Calmodulin-dependent Signaling
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
Feedback Regulation of Calcium Concentration
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...
Receptor-mediated Endocytosis
Membrane Asymmetry Regulating Transporters
Flippase
Eukaryotic flippases are type-IV P-type ATPases or P4-ATPases belonging to P-type ATPase family proteins that are membrane-bound pumps involved in the ATP-mediated transport of ions and molecules across the membrane. Flippases flip specific phospholipids from the outer to the inner leaflet of a membrane. All P4-ATPases have one...
Ligand-Gated Ion Channel Receptor: Gating Mechanism
