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关于细菌成分参与多聚核糖核苷酸对小鼠B淋巴细胞促有丝分裂特性的遗传和生化证据。

Genetic and biochemical evidence for the involvement of a bacterial component in the mitogenic properties of polyribonucleotides on murine B lymphocytes.

作者信息

Kelly K, Watson J

出版信息

J Immunol. 1979 Jun;122(6):2304-8.

PMID:312865
Abstract

The mitogenic response of C3H/HeJ mice to the B cell mitogens, poly C and poly I, is approximately one-half the response measured in various LPS-responder strains. C3H/HeJ mice respond normally to poly I:C, the heteroduplex polymer. The low responder phenotype of C3H/HeJ mice to poly C and poly I is shown by an analysis of (C3H/HeJ x C57BL/6J-By-Ps)F1 X C3H/HeJ backcross progeny to result from a gene locus that is closely linked or identical to the defective LPS response locus expressed by the C3H/HeJ strain. The entire mitogenic activity in poly C preparations and most of the mitogenic activity in poly I preparations is insensitive to ribonuclease degradation. Hot aqueous phenol extraction of the polynucleotides separates the majority of the mitogenic activity that is soluble in the combined interface and phenol phase fraction from the aqueous soluble polynucleotides. The ribonuclease-insensitive, phenolsoluble contaminant elicits a reduced response in C3H/HeJ mice as compared to an LPS responder strain. We conclude that 1) poly C has no inherent mitogenic activity; 2) poly I preparations contain both ribonucleasesensitive and insensitive mitogenic activities; 3) the ribonuclease-resistant mitogenic activity in polynucleotide preparations has properties unlike those of LPS or lipid A; and 4) the product of LPS response gene has an effect upon the mitogenic stimulation of spleen cells by the contaminant.

摘要

C3H/HeJ小鼠对B细胞促有丝分裂原多聚C和多聚I的促有丝分裂反应约为在各种LPS反应性品系中测得反应的一半。C3H/HeJ小鼠对异源双链聚合物多聚I:C反应正常。对(C3H/HeJ×C57BL/6J-By-Ps)F1与C3H/HeJ回交后代的分析表明,C3H/HeJ小鼠对多聚C和多聚I的低反应表型源于一个与C3H/HeJ品系所表达的缺陷LPS反应基因座紧密连锁或相同的基因座。多聚C制剂中的全部促有丝分裂活性以及多聚I制剂中的大部分促有丝分裂活性对核糖核酸酶降解不敏感。多核苷酸的热酚水提取将大部分可溶于合并的界面和酚相部分的促有丝分裂活性与水溶性多核苷酸分离。与LPS反应性品系相比,核糖核酸酶不敏感的酚溶性污染物在C3H/HeJ小鼠中引起的反应降低。我们得出以下结论:1)多聚C没有内在的促有丝分裂活性;2)多聚I制剂同时含有核糖核酸酶敏感和不敏感的促有丝分裂活性;3)多核苷酸制剂中抗核糖核酸酶的促有丝分裂活性具有与LPS或脂质A不同的特性;4)LPS反应基因的产物对污染物对脾细胞的促有丝分裂刺激有影响。

相似文献

1
Genetic and biochemical evidence for the involvement of a bacterial component in the mitogenic properties of polyribonucleotides on murine B lymphocytes.关于细菌成分参与多聚核糖核苷酸对小鼠B淋巴细胞促有丝分裂特性的遗传和生化证据。
J Immunol. 1979 Jun;122(6):2304-8.
2
LPS regulation of the immune response: separate mechanisms for murine B cell activation by lipid A (direct) and polysaccharide (macrophage-dependent) derived from Bacteroides LPS.脂多糖对免疫反应的调节:来自拟杆菌属脂多糖的脂质A(直接作用)和多糖(巨噬细胞依赖性)激活小鼠B细胞的不同机制。
J Immunol. 1984 Nov;133(5):2294-300.
3
LPS regulation of the immune response: Bacteroides endotoxin induces mitogenic, polyclonal, and antibody responses in classical LPS responsive but not C3H/HeJ mice.脂多糖对免疫反应的调节:类杆菌内毒素在经典的对脂多糖有反应的小鼠中可诱导促有丝分裂、多克隆和抗体反应,但在C3H/HeJ小鼠中则不然。
J Immunol. 1984 Jul;133(1):299-305.
4
Immunologic properties of bacterial lipopolysaccharide (LPS). IV. Cellular basis of the unresponsiveness of C3H/HeJ mouse spleen cells to LPS-induced mitogenesis.细菌脂多糖(LPS)的免疫学特性。IV. C3H/HeJ小鼠脾细胞对LPS诱导的有丝分裂原反应无反应性的细胞基础。
J Immunol. 1977 Jan;118(1):274-81.
5
Cellular mechanism of endotoxin unresponsiveness in C3H/HeJ mice.C3H/HeJ小鼠内毒素无反应性的细胞机制
J Immunol. 1976 Feb;116(2):454-61.
6
Immunostimulation of C3H/HeJ lymphoid cells by R-chemotype lipopolysaccharide preparations.R型化学型脂多糖制剂对C3H/HeJ淋巴细胞的免疫刺激作用。
J Immunol. 1989 Jan 15;142(2):642-52.
7
Differentiation of B lymphocytes in C3H/HeJ mice: the induction of Ia antigens by lipopolysaccharide.C3H/HeJ小鼠中B淋巴细胞的分化:脂多糖对Ia抗原的诱导作用。
J Immunol. 1977 Mar;118(3):1103-8.
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Partial restoration of the lipopolysaccharide-induced proliferative response in splenic B cells from C3H/HeJ mice.C3H/HeJ小鼠脾脏B细胞中脂多糖诱导的增殖反应的部分恢复。
J Immunol. 1986 Jul 15;137(2):472-7.
9
Mitogenic activity of Actinomyces viscosus. I. Effects on murine B and T lymphocytes, and partial characterization.黏性放线菌的促有丝分裂活性。I. 对小鼠B淋巴细胞和T淋巴细胞的影响及部分特性分析
J Immunol. 1977 Apr;118(4):1466-71.
10
Isolation of a lipid A bound polypeptide responsible for "LPS-initiated" mitogenesis of C3H/HeJ spleen cells.负责C3H/HeJ脾细胞“脂多糖引发”有丝分裂的脂多糖A结合多肽的分离。
J Exp Med. 1976 Sep 1;144(3):840-6. doi: 10.1084/jem.144.3.840.