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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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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. |
format | Online Article Text |
id | pubmed-3888388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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