免疫学杂志
免疫學雜誌
면역학잡지
IMMUNOLOGICAL JOURNAL
2000年
6期
457-460
,共4页
张新梅%林汉良%刘乐和%张昌卿%钟叔平%曾金云%郑克立
張新梅%林漢良%劉樂和%張昌卿%鐘叔平%曾金雲%鄭剋立
장신매%림한량%류악화%장창경%종숙평%증금운%정극립
食管癌旁组织%核基质%单克隆抗体
食管癌徬組織%覈基質%單剋隆抗體
식관암방조직%핵기질%단극륭항체
tissues adjacent to esophagus cancer%nuclear matrix%monoclonal antibody
目的 制备抗食管癌旁组织核基质蛋白的特异性单抗。方法 SDS-PAGE分析正常食管组织、食管癌旁组织及
食管癌组织核基质蛋白间的差异。用食管癌旁组织核基质蛋白做免疫原免疫Balb/c小鼠,利用杂交瘤技术制备了5株能稳定
分泌单克隆抗体的杂交瘤细胞株,并对9-1-2/D、9-1-7/D 2株细胞作了初步鉴定。结果 免疫组化分析发现9-1-2/D单抗与食管
癌及正常食管组织均有反应,而9-1-7/D单抗只与食管癌组织反应,与正常食管组织无反应。Western Blotting分析显示:
9-1-2/D单抗与电泳图谱上正常食管组织核基质和食管癌旁组织核基质52 kD的蛋白反应,而与食管癌组织核基质55 kD的蛋
白反应。9-1-7/D单抗只与电泳图谱上食管癌旁组织及癌组织核基质46 kD的蛋白反应,与正常食管组织核基质无反应。结论
本实验为食管癌的早期诊断作了初步有意义的探讨。
目的 製備抗食管癌徬組織覈基質蛋白的特異性單抗。方法 SDS-PAGE分析正常食管組織、食管癌徬組織及
食管癌組織覈基質蛋白間的差異。用食管癌徬組織覈基質蛋白做免疫原免疫Balb/c小鼠,利用雜交瘤技術製備瞭5株能穩定
分泌單剋隆抗體的雜交瘤細胞株,併對9-1-2/D、9-1-7/D 2株細胞作瞭初步鑒定。結果 免疫組化分析髮現9-1-2/D單抗與食管
癌及正常食管組織均有反應,而9-1-7/D單抗隻與食管癌組織反應,與正常食管組織無反應。Western Blotting分析顯示:
9-1-2/D單抗與電泳圖譜上正常食管組織覈基質和食管癌徬組織覈基質52 kD的蛋白反應,而與食管癌組織覈基質55 kD的蛋
白反應。9-1-7/D單抗隻與電泳圖譜上食管癌徬組織及癌組織覈基質46 kD的蛋白反應,與正常食管組織覈基質無反應。結論
本實驗為食管癌的早期診斷作瞭初步有意義的探討。
목적 제비항식관암방조직핵기질단백적특이성단항。방법 SDS-PAGE분석정상식관조직、식관암방조직급
식관암조직핵기질단백간적차이。용식관암방조직핵기질단백주면역원면역Balb/c소서,이용잡교류기술제비료5주능은정
분비단극륭항체적잡교류세포주,병대9-1-2/D、9-1-7/D 2주세포작료초보감정。결과 면역조화분석발현9-1-2/D단항여식관
암급정상식관조직균유반응,이9-1-7/D단항지여식관암조직반응,여정상식관조직무반응。Western Blotting분석현시:
9-1-2/D단항여전영도보상정상식관조직핵기질화식관암방조직핵기질52 kD적단백반응,이여식관암조직핵기질55 kD적단
백반응。9-1-7/D단항지여전영도보상식관암방조직급암조직핵기질46 kD적단백반응,여정상식관조직핵기질무반응。결론
본실험위식관암적조기진단작료초보유의의적탐토。
Objective To prepare anti-nuclear matrix proteins of tissues surrounding esophagus cancer monoclonal anti-
bodies. Methods Differences among nuclear matrix proteins (NMPS) of normal esophagus tissues, esophagus cancer tissues
and tissues adjacent to cancer were identified by SDS-PAGE. Balb/c mouse were hyperimmunized with NMPS of tissues adja-
cent to esophagus cancer. Five mouse lymphocyte hybridoma cell lines were established and preliminary identification of cell
lines 9-1-2/D, 9-1-7/D were made. Results Immunohistochemical analysis showed monoclonal antibody 9-1-2/D reacted both
with esophagus cancer and normal esophageal tissues; monoclonal antibody 9-1-7/D reacted only with nucleoli of esophagus
cancer cells. Western Blotting analysis showed monoclonal antibody 9-1-2/D reacted with 52 kD NMPS of normal esophagus
tissues and tissues adjacent to esophagus cancer and reacted with 55 kD NMP of esophagus cancer tissue. Monoclonal anti-
body 9-1-7/D reacted only with 46 kD protein of esophagus cancer tissues and tissues adjacent to cancer. Conclusion Mono-
clonal antibodies prepared by us might be a new method for early diagnosis of esophagus cancer.