Caveolin-1调节骨细胞中甲状旁腺激素(PTH)相关蛋白(PTHrP)对PTH受体1的作用

IF 4 2区 生物学 Q2 CELL BIOLOGY
Sara Heredero-Jiménez, Eduardo Martín-Guerrero, Joan Pizarro-Gómez, Irene Tirado-Cabrera, Luis Álvarez-Carrión, Teresita Bellido, Arancha R. Gortázar, Juan A. Ardura
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引用次数: 0

摘要

小窝蛋白-1 (Cav1)是一种存在于脂筏内陷的蛋白质,被称为小窝,调节一些细胞表面受体的运输和信号传导。目前的证据表明,小泡的数量可能随着年龄的增长而增加。甲状旁腺激素(PTH)受体1型(PTH1R)在PTH和PTH相关蛋白(PTHrP)肽激活后调节成骨细胞和骨细胞的行为。PTH1R的激活取决于它与不同的膜或细胞内分子的结合,从而导致确定的生物学效应。由于PTH1R显示出潜在的Cav1结合域,我们假设成骨细胞谱系中的PTH1R反应是由Cav1调节的,从而调节PTHrP在衰老过程中的作用。我们报道了Cav1在成骨细胞和骨细胞的膜微域与PTH1R共定位。在成骨细胞中,Cav1过表达通过降低细胞内钙积累和增加cAMP水平来改变pthrp依赖性信号,导致Runx2、骨钙素、骨碱性磷酸酶和OPG以快速和短暂的方式上调。相反,Cav1沉默导致ERK1/2激酶的过度磷酸化和钙的过度产生,从而导致Runx2、骨钙素和碱性磷酸酶的表达降低。体内小鼠骨中Cav1基因表达随年龄增长而增加,与Runx2、骨钙素、碱性磷酸酶呈负相关。此外,年龄依赖性的Cav-1过表达和小泡破坏与体外培养骨中pthrp依赖性骨基因表达的改变有关。FRAP分析显示,在受体激活后,Cav1导致PTH1R暂时滞留在Cav1微域,延迟PTH1R内化。我们得出结论,骨细胞中的PTH1R信号和PTHrP作用受Cav1调控,并且Cav1的过表达与年龄条件下骨中的PTH1R反应有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Caveolin-1 Regulates Parathyroid Hormone (PTH)-Related Protein (PTHrP) Actions on PTH Receptor Type 1 in Bone Cells

Caveolin-1 Regulates Parathyroid Hormone (PTH)-Related Protein (PTHrP) Actions on PTH Receptor Type 1 in Bone Cells

Caveolin-1 (Cav1), a protein present in lipid raft invaginations known as caveolae, regulates the trafficking and signaling of some cell surface receptors. Current evidence suggests that the number of caveolae might increase with aging. The parathyroid hormone (PTH) receptor type 1 (PTH1R) regulates osteoblast and osteocyte actions after activation by PTH and PTH-related protein (PTHrP) peptides. PTH1R activation leads to defined biological effects depending on its association with different membrane or intracellular molecules. Since PTH1R exhibits a potential Cav1 binding domain, we hypothesized that PTH1R responses are regulated by Cav1 in cells of the osteoblastic lineage, conditioning PTHrP actions during aging. We report that Cav1 colocalizes with PTH1R at membrane microdomains in osteoblastic and osteocytic cells. Cav1 overexpression modifies PTHrP-dependent signaling in osteoblastic cells by decreasing intracellular calcium accumulation and increasing cAMP levels leading to upregulation of Runx2, osteocalcin, bone alkaline phosphatase, and OPG in a rapid and transient manner. Conversely, Cav1 silencing causes over-phosphorylation of ERK1/2 kinase and overproduction of calcium, which leads to reduced expression of Runx2, osteocalcin, and alkaline phosphatase. Further, the gene expression of Cav1 increases with age in murine bone in vivo and negatively correlates with that of Runx2, osteocalcin and alkaline phosphatase. Moreover, age-dependent overexpression of Cav-1 and caveolae disruption is associated with alterations in PTHrP-dependent bone gene expression in ex vivo cultured bones. FRAP analysis revealed that Cav1 causes PTH1R temporary retention at Cav1 microdomains upon receptor activation, delaying PTH1R internalization. We conclude that PTH1R signaling and PTHrP actions in bone cells are regulated by Cav1 and that Cav1 overexpression with age conditions PTH1R responses in bone.

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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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