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组蛋白去乙酰化酶5是破骨细胞中蛋白激酶D的磷酸化底物。

Histone deacetylase 5 is a phosphorylation substrate of protein kinase D in osteoclasts.

作者信息

Meyers Carina Mello Guimaraes, Burciaga Samuel D, Faulkner Bora, Kazemi Parandis, Cohn Jacob M, Mansky Kim C, Jensen Eric D

机构信息

Department of Diagnostic & Biological Sciences, University of Minnesota School of Dentistry, Minneapolis, MN 55455, USA.

Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Bone. 2022 Jun;159:116393. doi: 10.1016/j.bone.2022.116393. Epub 2022 Mar 19.

Abstract

Protein kinase D (PRKD) family kinases are required for formation and function of osteoclasts. However, the substrates of PRKD in osteoclasts are unknown. To identify PRKD-dependent protein phosphorylation in osteoclasts, we performed a quantitative LC-MS/MS phosphoproteomics screen for proteins showing differential phosphorylation in osteoclasts after treatment with the PRKD inhibitor CRT0066101. We identified 757 phosphopeptides showing significant changes following PRKD inhibition. Among the changes, we found a group of 13 proteins showing decreased phosphorylation at PRKD consensus phosphorylation motifs. This group includes histone deacetylase 5 (HDAC5), which is a previously validated PRKD target. Considering this known interaction, work suggesting HDACs may be important regulators of osteoclasts, and studies suggesting potential functional redundancy between HDACs, we further investigated the relationship between PRKD and class IIa HDACs in osteoclasts. We confirmed that CRT0066101 inhibits phosphorylation of endogenous HDAC5 and to a lesser extent HDAC4, whereas HDAC7 phosphorylation was not affected. Osteoclast cultures from Hdac5 global knockout mice displayed impaired differentiation and reduced ability to resorb bone, while conditional knockout of Hdac4 in osteoclasts showed no phenotype in vitro or in vivo. The inhibitory effect of CRT0066101 was reduced in Hdac5 KO osteoclasts. Together these data indicate that the PRKD/HDAC5 axis contributes to osteoclast formation in vitro and suggest that this pathway may contribute to regulation of skeletal dynamics in vivo.

摘要

蛋白激酶D(PRKD)家族激酶是破骨细胞形成和功能所必需的。然而,破骨细胞中PRKD的底物尚不清楚。为了鉴定破骨细胞中PRKD依赖性蛋白磷酸化,我们进行了定量液相色谱-串联质谱磷酸化蛋白质组学筛选,以寻找在用PRKD抑制剂CRT0066101处理后的破骨细胞中显示出磷酸化差异的蛋白质。我们鉴定出757个磷酸肽在PRKD抑制后显示出显著变化。在这些变化中,我们发现一组13种蛋白质在PRKD共有磷酸化基序处的磷酸化减少。该组包括组蛋白去乙酰化酶5(HDAC5),它是先前已验证的PRKD靶标。考虑到这种已知的相互作用、提示HDACs可能是破骨细胞重要调节因子的研究以及提示HDACs之间存在潜在功能冗余的研究,我们进一步研究了破骨细胞中PRKD与IIa类HDACs之间的关系。我们证实CRT0066101抑制内源性HDAC5的磷酸化,对HDAC4的抑制作用较小,而HDAC7的磷酸化不受影响。来自Hdac5基因敲除小鼠的破骨细胞培养物显示分化受损且骨吸收能力降低,而破骨细胞中Hdac4的条件性敲除在体外或体内均未显示出表型。CRT0066101对Hdac5基因敲除破骨细胞的抑制作用减弱。这些数据共同表明PRKD/HDAC5轴在体外有助于破骨细胞形成,并提示该途径可能在体内对骨骼动力学调节起作用。

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