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作 者:张新波[1] 汤乃梅[1] 夏泉[1] 齐俊明 朱正美[1] 崔肇春[1]
出 处:《中国病理生理杂志》1995年第6期582-586,共5页Chinese Journal of Pathophysiology
基 金:自然科学基金
摘 要:将J6-2细胞分别用分化诱导剂GM_3(50μmol/L)、DMSO(1.2%)处理6天、TPA(10ng/ml)处理3天,观察它们对11种凝集素结合反应的影响。结果表明,经GM_3处理后,J6-2细胞对凝集素结合反应增强的只有UEA(-至+),变弱的只有BSA(++至-),其余的都无变化。经DMSO处理后,结合反应变强的有UEA(-至+)及PNA(-至++),变弱的有BSA(++至-)及PSA(++至+)。经TPA处理后,结合反应变弱的有BSA(++至+)、WGA(++至-)及RCA(++至+),变强的有UEA(-至+)、SBA(-至+)及SJA(-至++)。对3种分化诱导剂处理后都无变化的有DBA(-)、LCA(++)及ConA(++)。本文还观察到3种分化诱导剂都能抑制[ ̄125I]UdR向J6-2细胞的掺入。The effect of treating human monocytoid J6-2 leukemic cell s with cell differentiation inducers on the lectin binding capacities and on the incorporation of [ ̄125I]UdR into J6-2 cells was studied.The lectins used were BSA,ConA,DBA,LCA,PNA,PSA,RCA,SBA,SJA,UEA,and WGA.The results reveal that after 6-day treatment with GM_3(concentration,50μmol/L, the binding capacity( BC )of J6-2 cells for UEA increased(-→+), that for BSA decreased(++→-),while those for others rema- inded unchanged;after 6-day treatment with DMSO (1.2%),the BC for UEA(-→+)and PNA(-→++)increased,those for BSA(++→-)and for PSA (++→+)decreased;after 3-day treatment with TPA(10ng/ml),the BC for UEA (-→+),SBA(-→+)and SJA (-→++)increased, while those for BSA ( ++→+),RCA (++→+), and WGA(++→-)decreased.The BC for DBA (-),LCA ( ++ ),and ConA(++)remained unchanged to treatments with all 3 differentiation inducers.Discussion was directed to the change of carbohydrate structure with respect to change of lectin binding capacity.The results also reveal that after treatment of J6-2 cells with the above mentioned 3 differentiation inducers,the incorporation of[ ̄125I]UdR into J6-2 cells all decreased.This indicates that the DNA synthesis of J6-2 cells was inhibited by the treatment of the differentiation inducers used in this study.
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