Ushio S, Iwaki K, Taniai M, Ohta T, Fukuda S, Sugimura K, Kurimoto M
Fujisaki Institute, Hayashibara Biochemical Laboratories, Inc., Okayama, Japan.
Microbiol Immunol. 1995;39(6):393-400. doi: 10.1111/j.1348-0421.1995.tb02218.x.
We found that mycoplasma-infected cells have a higher ability to metastasize in vivo than non-mycoplasma-infected cells. To investigate this phenomenon, we obtained a monoclonal antibody, MAb 243-5, by immunization with Mycoplasma arginini-infected RPMI 4788 cells. This MAb recognized a mycoplasmal protein with an MW of 47 kDa and completely inhibited the experimental metastasis of M. arginini-infected RPMI 4788 cells using a nude mouse model. Using this MAb, we purified a molecule called Ag 243-5 and determined the N-terminal amino acid sequence and clarified the entire nucleotide sequence of the Ag 243-5 gene. PCR analysis showed the existence of a homologous gene in Mycoplasma hyorhinis. Four sequential injections of Ag 243-5 (30 micrograms/shot) promoted the experimental metastasis of non-mycoplasma-infected RPMI 4788 cells more than 10-fold using a nude mouse model. Ag 243-5 also promoted the experimental metastasis of the non-mycoplasma-infected mouse colon cancer cell line colon 26. This metastasis-promoting effect was neutralized by MAb 243-5.
我们发现,支原体感染的细胞在体内的转移能力高于未感染支原体的细胞。为了研究这一现象,我们用精氨酸支原体感染的RPMI 4788细胞进行免疫,获得了一种单克隆抗体MAb 243-5。这种单克隆抗体识别一种分子量为47 kDa的支原体蛋白,并使用裸鼠模型完全抑制了精氨酸支原体感染的RPMI 4788细胞的实验性转移。利用这种单克隆抗体,我们纯化了一种名为Ag 243-5的分子,确定了其N端氨基酸序列,并阐明了Ag 243-5基因的完整核苷酸序列。PCR分析显示猪鼻支原体中存在同源基因。使用裸鼠模型,四次连续注射Ag 243-5(30微克/次)使未感染支原体的RPMI 4788细胞的实验性转移增加了10倍以上。Ag 243-5还促进了未感染支原体的小鼠结肠癌细胞系colon 26的实验性转移。这种转移促进作用被MAb 243-5中和。