Department of Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Department of Organic Chemistry, School of Pharmaceutical Sciences, Hiroshima International University, Hiroshima, Japan.
PLoS One. 2014 Jan 10;9(1):e81941. doi: 10.1371/journal.pone.0081941. eCollection 2014.
Sialidase removes sialic acid from sialoglycoconjugates and plays crucial roles in many physiological and pathological processes. Various human cancers express an abnormally high level of the plasma membrane-associated sialidase isoform.Visualization of sialidase activity in living mammalian tissues would be useful not only for understanding sialidase functions but also for cancer diagnosis. However, since enzyme activity of mammalian sialidase is remarkably weak compared with that of bacterial and viral sialidases, it has been difficult to detect sialidase activity in mammalian tissues. We synthesized a novel benzothiazolylphenol-based sialic acid derivative (BTP-Neu5Ac) as a fluorescent sialidase substrate. BTP-Neu5Ac can visualize sialidase activities sensitively and selectively in acute rat brain slices. Cancer cells implanted orthotopically in mouse colons and human colon cancers (stages T3-T4) were also clearly detected with BTP-Neu5Ac. The results suggest that BTP-Neu5Ac is useful for histochemical imaging of sialidase activities.
唾液酸酶从唾液酸化糖缀合物中去除唾液酸,并在许多生理和病理过程中发挥关键作用。各种人类癌症表达异常高水平的质膜相关唾液酸酶同工型。在活体哺乳动物组织中可视化唾液酸酶活性不仅有助于理解唾液酸酶的功能,还有助于癌症诊断。然而,由于与细菌和病毒唾液酸酶相比,哺乳动物唾液酸酶的酶活性显著较弱,因此很难在哺乳动物组织中检测到唾液酸酶活性。我们合成了一种新型苯并噻唑基苯酚基唾液酸衍生物(BTP-Neu5Ac)作为荧光唾液酸酶底物。BTP-Neu5Ac 可以在急性大鼠脑片中敏感且选择性地可视化唾液酸酶活性。用 BTP-Neu5Ac 也可以清楚地检测到原位植入小鼠结肠和人结肠癌(T3-T4 期)的癌细胞。结果表明,BTP-Neu5Ac 可用于唾液酸酶活性的组织化学成像。