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dc.contributor.authorDebacq-Chainiaux, Florence
dc.contributor.authorErusalimsky, Jorge
dc.contributor.authorCampisi, Judith
dc.contributor.authorToussaint, Olivier
dc.date.accessioned2014-02-11T09:10:47Z
dc.date.available2014-02-11T09:10:47Z
dc.date.issued2009
dc.identifier.citationNature Protocols 4 (12), pp. 1798 - 1806 (2009)en_US
dc.identifier.issn1754-2189
dc.identifier.urihttp://hdl.handle.net/10369/5286
dc.description.abstractNormal cells can permanently lose the ability to proliferate when challenged by potentially oncogenic stress, a process termed cellular senescence. Senescence-associated beta-galactosidase (SASA-βgal) activity, detectable at pH 6.0, permits the identification of senescent cells in culture and mammalian tissues. Here we describe first a cytochemical protocol suitable for the histochemical detection of individual senescent cells both in culture and tissue biopsies. The second method is based on the alkalinization of lysosomes, followed by the use of 5-dodecanoylaminofluorescein di-β-D-galactopyranoside (C12FDG), a fluorogenic substrate for βgal activity. The cytochemical method takes about 30 min to execute, and several hours to a day to develop and score. The fluorescence methods take between 4 and 8 h to execute and can be scored in a single day. The cytochemical method is applicable to tissue sections and requires simple reagents and equipment. The fluorescence-based methods have the advantages of being more quantitative and sensitive.en_US
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.relation.ispartofseriesNature Protocols;
dc.titleProtocols to detect senescence-associated beta-galactosidase (SA-βgal) activity, a biomarker of senescent cells in culture and in vivoen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1038/nprot.2009.191


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