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首页> 外文期刊>Archives of medical research >Sodium caseinate induces expression and secretion of murine multipotent myeloid cell line 32D macrophage colony-stimulating factor.
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Sodium caseinate induces expression and secretion of murine multipotent myeloid cell line 32D macrophage colony-stimulating factor.

机译:酪蛋白酸钠诱导鼠多能骨髓细胞系32D巨噬细胞集落刺激因子的表达和分泌。

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BACKGROUND: Evidence that sodium caseinate (CasNa) is capable of inhibiting proliferation of hematopoietic precursor cell line 32D and inducing its differentiation into macrophage cells has recently been published. Taking into consideration that hematopoiesis is regulated by growth factors and that macrophage colony-stimulating factor (M-CSF) is a well-known growth factor that induces differentiation of macrophages, in this work we evaluated whether CasNa is capable of inducing expression and secretion of M-CSF in 32D cells. METHODS: We cultured 32D cells in presence and absence of CasNa and compared their proliferation and viability. RNA was extracted from cell lysates to evaluate expression of the gene for M-CSF and its receptor. Cultured conditioned media was used to evaluate presence of M-CSF. RESULTS: Our results showed that CasNa inhibited proliferation of 32D cells and that conditioned media (CM) of these cultures contained M-CSF-like activity. Presence of M-CSF in CM was detected by inhibiting M-CSF activity with anti-M-CSF and presence of this growth factor was confirmed by ELISA assay. We also provided evidence that CasNa induced expression of mRNA for M-CSF in 32D cells as well as increased expression of mRNA for its receptor. CONCLUSIONS: CasNa inhibits proliferation of 32D cells and induces expression of the gene for M-CSF and that of its receptor. It also induces secretion of the bioactive form of M-CSF.
机译:背景:酪蛋白酸钠(CasNa)能够抑制造血前体细胞系32D的增殖并诱导其分化为巨噬细胞的证据最近已经发表。考虑到造血功能受生长因子的调节,而巨噬细胞集落刺激因子(M-CSF)是诱导巨噬细胞分化的众所周知的生长因子,因此在这项工作中,我们评估了CasNa是否能够诱导巨噬细胞的表达和分泌。 32D细胞中的M-CSF。方法:我们在存在和不存在CasNa的情况下培养32D细胞,并比较它们的增殖和生存能力。从细胞裂解物中提取RNA,以评估M-CSF及其受体基因的表达。培养的条件培养基用于评估M-CSF的存在。结果:我们的结果表明,CasNa抑制32D细胞的增殖,并且这些培养物的条件培养基(CM)均具有M-CSF样活性。通过用抗M-CSF抑制M-CSF活性来检测CM中M-CSF的存在,并通过ELISA分析确认了该生长因子的存在。我们还提供了CasNa诱导32D细胞中M-CSF mRNA表达以及其受体mRNA表达增加的证据。结论:CasNa抑制32D细胞的增殖,并诱导M-CSF基因及其受体的表达。它还诱导M-CSF的生物活性形式的分泌。

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