Martin Aline, Kawaguchi Riki, Wang Qing, Salusky Isidro B, Pereira Renata C, Wesseling-Perry Katherine
Division of Nephrology and Hypertension, Center for Translational Metabolism and Health, Feinberg Cardiovascular and Renal Research Institute, Northwestern University, Evanston, IL 60208.
Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095.
JBMR Plus. 2024 Jan 4;8(1):ziad015. doi: 10.1093/jbmrpl/ziad015. eCollection 2024 Jan.
Maturation defects are intrinsic features of osteoblast lineage cells in CKD patients. These defects persist ex vivo, suggesting that CKD induces epigenetic changes in bone cells. To gain insights into which signaling pathways contribute to CKD-mediated, epigenetically driven, impairments in osteoblast maturation, we characterized RNA expression and DNA methylation patterns by RNA-Seq and MethylationEpic in primary osteoblasts from nine adolescent and young adult dialysis patients with end-stage kidney disease and three healthy references. ATAC-Seq was also performed on a subset of osteoblasts. Bone matrix protein expression was extracted from the iliac crest and evaluated by proteomics. Gene set enrichment analysis was used to establish signaling pathways consistently altered in chromatin accessibility, DNA methylation, and RNA expression patterns. Single genes were suppressed in primary osteoblasts using shRNA and mineralization characterized in vitro. The effect of nuclear factor of activated T cells (NFAT) signaling suppression was also assessed using 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) incorporation. We found that signaling pathways critical for osteoblast differentiation were strongly downregulated in CKD osteoblasts. Gene set enrichment analysis identified highly significant methylation changes, differential chromatin accessibility, and altered RNA expression in NFAT signaling targets. NFAT inhibition reduced osteoblast proliferation. Combined analysis of osteoblast RNA expression and whole bone matrix composition identified 13 potential ligand-receptor pairs. In summary, epigenetic changes in CKD osteoblasts associate with altered expression of multiple osteoblast genes and signaling pathways. An increase in NFAT signaling may play a role in impaired CKD osteoblast maturation. Epigenetic changes also associate with an altered bone matrix, which may contribute to bone fragility. Further studies are necessary to elucidate the pathways affected by these genetic alterations since elucidating these pathways will be vital to correcting the underlying biology of bone disease in the CKD population.
成熟缺陷是慢性肾脏病(CKD)患者成骨细胞系细胞的内在特征。这些缺陷在体外持续存在,表明CKD会诱导骨细胞发生表观遗传变化。为了深入了解哪些信号通路导致了CKD介导的、表观遗传驱动的成骨细胞成熟受损,我们通过RNA测序(RNA-Seq)和甲基化芯片(MethylationEpic)对9名青少年和青年成年终末期肾病透析患者及3名健康对照者的原代成骨细胞的RNA表达和DNA甲基化模式进行了表征。还对一部分成骨细胞进行了转座酶可接近染色质测序(ATAC-Seq)。从髂嵴提取骨基质蛋白表达,并通过蛋白质组学进行评估。基因集富集分析用于确定在染色质可及性、DNA甲基化和RNA表达模式中持续改变的信号通路。使用短发夹RNA(shRNA)在原代成骨细胞中抑制单个基因,并在体外对矿化进行表征。还使用3-(4,5-二甲基噻唑-2-基)-5-(3-羧甲氧基苯基)-2-(4-磺基苯基)-2H-四唑(MTS)掺入法评估活化T细胞核因子(NFAT)信号抑制的作用。我们发现,对成骨细胞分化至关重要的信号通路在CKD成骨细胞中强烈下调。基因集富集分析确定了NFAT信号靶点中高度显著的甲基化变化、染色质可及性差异和RNA表达改变。抑制NFAT可降低成骨细胞增殖。对成骨细胞RNA表达和全骨基质组成的联合分析确定了13对潜在的配体-受体对。总之,CKD成骨细胞中的表观遗传变化与多个成骨细胞基因和信号通路的表达改变有关。NFAT信号增加可能在CKD成骨细胞成熟受损中起作用。表观遗传变化还与骨基质改变有关,这可能导致骨脆性增加。由于阐明这些途径对于纠正CKD人群骨病的潜在生物学机制至关重要,因此有必要进一步研究以阐明受这些基因改变影响的途径。