Harada Y, Nagao S, Nakamura M, Okada F, Tanigawa Y
Department of Biochemistry, Shimmane Medical University, Izumo, Japan.
Immunology. 1995 Feb;84(2):247-53.
Lipopolysaccharide (LPS), known as one of the potent activators of macrophages, has inhibitory effects on the proliferation of normal macrophages and macrophage-like cell lines. We report here that LPS dose- and time-dependently suppressed the tritiated thymidine ([3H]TdR) incorporation into the acid-insoluble fraction with a significant inverse correlation to the tumour necrosis factor-alpha (TNF) production in the J774.1 macrophage cell line. Among the three tested enzymes involved in DNA synthesis, only thymidine kinase (TK) activity decreased progressively in parallel with the decline in [3H]TdR incorporation, reaching 97% inhibition within 12 hr of LPS treatment, while changes in the activities of other two enzymes, DNA polymerase alpha and thymidylate synthase (TS), were less significant. On the other hand, LPS inhibited the cell proliferation only incompletely, as judged by 62% inhibition of cell growth at 36 hr. Even in the experiments done in a TdR-free medium, cell growth was inhibited by LPS to the same extent, suggesting that TK was not directly involved in the proliferation of J774 cells. LPS also inhibited the conversion of TdR to thymidine monophosphate (TMP) in murine peritoneal exudate macrophages (PEM). Thus LPS-induced suppression of TdR salvage related to TNF production is common in both normal and neoplastic macrophages, and therefore may be of potential importance in the process of macrophage activation.
脂多糖(LPS)是巨噬细胞的强效激活剂之一,对正常巨噬细胞和巨噬细胞样细胞系的增殖具有抑制作用。我们在此报告,LPS在J774.1巨噬细胞系中剂量和时间依赖性地抑制了氚标记胸腺嘧啶核苷([3H]TdR)掺入酸不溶性部分,且与肿瘤坏死因子-α(TNF)的产生呈显著负相关。在参与DNA合成的三种测试酶中,只有胸苷激酶(TK)活性随着[3H]TdR掺入的下降而逐渐降低,在LPS处理12小时内达到97%的抑制率,而另外两种酶,DNA聚合酶α和胸苷酸合成酶(TS)的活性变化则不太显著。另一方面,LPS仅不完全抑制细胞增殖,36小时时细胞生长抑制率为62%。即使在无TdR培养基中进行的实验中,LPS对细胞生长的抑制程度相同,这表明TK并不直接参与J774细胞的增殖。LPS还抑制了小鼠腹腔渗出巨噬细胞(PEM)中TdR向胸苷一磷酸(TMP)的转化。因此,LPS诱导的与TNF产生相关的TdR补救途径抑制在正常和肿瘤性巨噬细胞中都很常见,因此可能在巨噬细胞激活过程中具有潜在重要性。