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癸酸抑制脂多糖诱导破骨细胞分化过程中 NO 的产生和 STAT3 的激活。

Capric acid inhibits NO production and STAT3 activation during LPS-induced osteoclastogenesis.

机构信息

Department of Molecular Science and Technology, Ajou University, Suwon, Korea.

出版信息

PLoS One. 2011;6(11):e27739. doi: 10.1371/journal.pone.0027739. Epub 2011 Nov 16.

Abstract

Capric acid is a second medium-chain fatty acid, and recent studies have shown that fatty acids are associated with bone density and reduce bone turnover. In this study, we investigated the effects of capric acid on lipopolysaccharide (LPS)-induced osteoclastogenesis in RAW264.7 cells. After treatment with capric acid (1 mM), the number of tartrate resistant acid phosphatase (TRAP)-positive cells decreased significantly. Capric acid reduced LPS-induced TRAP expression, an osteoclast differentiation marker, without inhibiting cell viability. LPS strongly upregulated inducible nitric oxide synthase (iNOS) mRNA levels and nitric oxide (NO) production, whereas capric acid inhibited them. Furthermore, capric acid also inhibited monocyte chemoattractant protein-1 (MCP-1) mRNA expression. Subsequently, we investigated various intracellular signaling proteins, including nuclear factor-κB (NF-κB), c-Jun-N-terminal kinase (JNK), extracellular signal regulated kinase 1/2 (ERK1/2), and signal transducer and activator of transcription 1 (STAT1) and STAT3 associated with osteoclastogenesis. Capric acid had no effects on LPS-induced activation of the NF-κB, JNK, ERK1/2, and STAT1 pathways. However, capric acid inhibited LPS-induced phosphorylation of Ser(727) in STAT3. Additionally, stattic (a STAT3 inhibitor) inhibited LPS-induced iNOS and MCP-1 gene expression. In conclusion, we demonstrated that capric acid inhibited LPS-induced osteoclastogenesis by suppressing NO production via the STAT3 pathway. These results suggest that capric acid has important therapeutic implications for treating bone diseases associated with excessive osteoclastogenesis.

摘要

癸酸是第二种中链脂肪酸,最近的研究表明,脂肪酸与骨密度有关,并能减少骨转换。在本研究中,我们研究了癸酸对 RAW264.7 细胞中脂多糖(LPS)诱导的破骨细胞形成的影响。用癸酸(1mM)处理后,抗酒石酸酸性磷酸酶(TRAP)阳性细胞的数量明显减少。癸酸降低了 LPS 诱导的破骨细胞分化标志物 TRAP 的表达,而不抑制细胞活力。LPS 强烈地上调诱导型一氧化氮合酶(iNOS)mRNA 水平和一氧化氮(NO)的产生,而癸酸抑制了它们。此外,癸酸还抑制单核细胞趋化蛋白-1(MCP-1)mRNA 的表达。随后,我们研究了各种与破骨细胞形成有关的细胞内信号蛋白,包括核因子-κB(NF-κB)、c-Jun-N-末端激酶(JNK)、细胞外信号调节激酶 1/2(ERK1/2)和信号转导和转录激活因子 1(STAT1)和 STAT3。癸酸对 LPS 诱导的 NF-κB、JNK、ERK1/2 和 STAT1 途径的激活没有影响。然而,癸酸抑制了 LPS 诱导的 STAT3 中 Ser(727)的磷酸化。此外,stattic(一种 STAT3 抑制剂)抑制了 LPS 诱导的 iNOS 和 MCP-1 基因表达。总之,我们证明癸酸通过抑制 STAT3 途径抑制 LPS 诱导的破骨细胞形成来抑制 NO 的产生。这些结果表明,癸酸对治疗与破骨细胞过度形成相关的骨疾病具有重要的治疗意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e19/3218024/52bba43e53f0/pone.0027739.g001.jpg

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