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Visualization of Sialidase Activity in Mammalian Tissues and Cancer Detection with a Novel Fluorescent Sialidase Substrate

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...

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Detalles Bibliográficos
Autores principales: Minami, Akira, Otsubo, Tadamune, Ieno, Daisuke, Ikeda, Kiyoshi, Kanazawa, Hiroaki, Shimizu, Kosuke, Ohata, Ko, Yokochi, Tsunehiro, Horii, Yuuki, Fukumoto, Hokuto, Taguchi, Risa, Takahashi, Tadanobu, Oku, Naoto, Suzuki, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888388/
https://www.ncbi.nlm.nih.gov/pubmed/24427265
http://dx.doi.org/10.1371/journal.pone.0081941
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author Minami, Akira
Otsubo, Tadamune
Ieno, Daisuke
Ikeda, Kiyoshi
Kanazawa, Hiroaki
Shimizu, Kosuke
Ohata, Ko
Yokochi, Tsunehiro
Horii, Yuuki
Fukumoto, Hokuto
Taguchi, Risa
Takahashi, Tadanobu
Oku, Naoto
Suzuki, Takashi
author_facet Minami, Akira
Otsubo, Tadamune
Ieno, Daisuke
Ikeda, Kiyoshi
Kanazawa, Hiroaki
Shimizu, Kosuke
Ohata, Ko
Yokochi, Tsunehiro
Horii, Yuuki
Fukumoto, Hokuto
Taguchi, Risa
Takahashi, Tadanobu
Oku, Naoto
Suzuki, Takashi
author_sort Minami, Akira
collection PubMed
description 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.
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spelling pubmed-38883882014-01-14 Visualization of Sialidase Activity in Mammalian Tissues and Cancer Detection with a Novel Fluorescent Sialidase Substrate Minami, Akira Otsubo, Tadamune Ieno, Daisuke Ikeda, Kiyoshi Kanazawa, Hiroaki Shimizu, Kosuke Ohata, Ko Yokochi, Tsunehiro Horii, Yuuki Fukumoto, Hokuto Taguchi, Risa Takahashi, Tadanobu Oku, Naoto Suzuki, Takashi PLoS One Research Article 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. Public Library of Science 2014-01-10 /pmc/articles/PMC3888388/ /pubmed/24427265 http://dx.doi.org/10.1371/journal.pone.0081941 Text en © 2014 Minami et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Minami, Akira
Otsubo, Tadamune
Ieno, Daisuke
Ikeda, Kiyoshi
Kanazawa, Hiroaki
Shimizu, Kosuke
Ohata, Ko
Yokochi, Tsunehiro
Horii, Yuuki
Fukumoto, Hokuto
Taguchi, Risa
Takahashi, Tadanobu
Oku, Naoto
Suzuki, Takashi
Visualization of Sialidase Activity in Mammalian Tissues and Cancer Detection with a Novel Fluorescent Sialidase Substrate
title Visualization of Sialidase Activity in Mammalian Tissues and Cancer Detection with a Novel Fluorescent Sialidase Substrate
title_full Visualization of Sialidase Activity in Mammalian Tissues and Cancer Detection with a Novel Fluorescent Sialidase Substrate
title_fullStr Visualization of Sialidase Activity in Mammalian Tissues and Cancer Detection with a Novel Fluorescent Sialidase Substrate
title_full_unstemmed Visualization of Sialidase Activity in Mammalian Tissues and Cancer Detection with a Novel Fluorescent Sialidase Substrate
title_short Visualization of Sialidase Activity in Mammalian Tissues and Cancer Detection with a Novel Fluorescent Sialidase Substrate
title_sort visualization of sialidase activity in mammalian tissues and cancer detection with a novel fluorescent sialidase substrate
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888388/
https://www.ncbi.nlm.nih.gov/pubmed/24427265
http://dx.doi.org/10.1371/journal.pone.0081941
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