Dissecting lysosomal viscosity fluctuations in live cells and liver tissues with an ingenious NIR fluorescent probe
Viscosity is a pivotal component in the cell microenvironment, while lysosomal viscosity fluctuation is associated with various human diseases, such as tumors and liver diseases. Herein, a near-infrared fluorescent probe (BIMM) based on merocyanine dyes was designed and synthesized for detecting lys...
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Veröffentlicht in: | Talanta (Oxford) 2024-05, Vol.272, p.125825-125825, Article 125825 |
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description | Viscosity is a pivotal component in the cell microenvironment, while lysosomal viscosity fluctuation is associated with various human diseases, such as tumors and liver diseases. Herein, a near-infrared fluorescent probe (BIMM) based on merocyanine dyes was designed and synthesized for detecting lysosomal viscosity in live cells and liver tissue. The increase in viscosity restricts the free rotation of single bonds, leading to enhanced fluorescence intensity. BIMM exhibits high sensitivity and good selectivity, and is applicable to a wide pH range. BIMM has near-infrared emission, and the fluorescent intensity shows an excellent linear relationship with viscosity. Furthermore, BIMM possessing excellent lysosomes-targeting ability, and can monitor viscosity changes in live cells stimulated by dexamethasone, lipopolysaccharide (LPS), and nigericin, and differentiate between cancer cells and normal cells. Noticeably, BIMM can accurately analyze viscosity changes in various liver disease models with HepG2 cells, and is successfully utilized to visualize variations in viscosity on APAP-induced liver injury. All the results demonstrated that BIMM is a powerful wash-free tool to monitor the viscosity fluctuations in living systems.
[Display omitted]
•An ingenious near-infrared fluorescent probe (BIMM) for sensitively detecting viscosity was reported.•BIMM could effectively target lysosomes and observe changes of lysosomal viscosity in living cells.•BIMM could differentiate between cancer cells and normal cells.•BIMM was successfully used for imaging viscosity variation in liver injury. |
doi_str_mv | 10.1016/j.talanta.2024.125825 |
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[Display omitted]
•An ingenious near-infrared fluorescent probe (BIMM) for sensitively detecting viscosity was reported.•BIMM could effectively target lysosomes and observe changes of lysosomal viscosity in living cells.•BIMM could differentiate between cancer cells and normal cells.•BIMM was successfully used for imaging viscosity variation in liver injury.</description><identifier>ISSN: 0039-9140</identifier><identifier>EISSN: 1873-3573</identifier><identifier>DOI: 10.1016/j.talanta.2024.125825</identifier><identifier>PMID: 38417371</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Bioimaging ; Fluorescent Dyes - chemistry ; Fluorescent probe ; HeLa Cells ; Hep G2 Cells ; Humans ; Liver ; Liver diseases ; Lysosomes ; Lysosomes - chemistry ; Viscosity</subject><ispartof>Talanta (Oxford), 2024-05, Vol.272, p.125825-125825, Article 125825</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c313t-136325e279fe73cb393d6f58f99e16cd54e369233c7f850ba69319d27832f4e63</cites><orcidid>0000-0002-4888-5181</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.talanta.2024.125825$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38417371$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Jiang, Qingqing</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Fang, Yuqi</creatorcontrib><creatorcontrib>Zhang, Peng</creatorcontrib><creatorcontrib>Wei, Liangchen</creatorcontrib><creatorcontrib>Li, Dongpeng</creatorcontrib><creatorcontrib>Shu, Wei</creatorcontrib><creatorcontrib>Xiao, Haibin</creatorcontrib><title>Dissecting lysosomal viscosity fluctuations in live cells and liver tissues with an ingenious NIR fluorescent probe</title><title>Talanta (Oxford)</title><addtitle>Talanta</addtitle><description>Viscosity is a pivotal component in the cell microenvironment, while lysosomal viscosity fluctuation is associated with various human diseases, such as tumors and liver diseases. Herein, a near-infrared fluorescent probe (BIMM) based on merocyanine dyes was designed and synthesized for detecting lysosomal viscosity in live cells and liver tissue. The increase in viscosity restricts the free rotation of single bonds, leading to enhanced fluorescence intensity. BIMM exhibits high sensitivity and good selectivity, and is applicable to a wide pH range. BIMM has near-infrared emission, and the fluorescent intensity shows an excellent linear relationship with viscosity. Furthermore, BIMM possessing excellent lysosomes-targeting ability, and can monitor viscosity changes in live cells stimulated by dexamethasone, lipopolysaccharide (LPS), and nigericin, and differentiate between cancer cells and normal cells. Noticeably, BIMM can accurately analyze viscosity changes in various liver disease models with HepG2 cells, and is successfully utilized to visualize variations in viscosity on APAP-induced liver injury. All the results demonstrated that BIMM is a powerful wash-free tool to monitor the viscosity fluctuations in living systems.
[Display omitted]
•An ingenious near-infrared fluorescent probe (BIMM) for sensitively detecting viscosity was reported.•BIMM could effectively target lysosomes and observe changes of lysosomal viscosity in living cells.•BIMM could differentiate between cancer cells and normal cells.•BIMM was successfully used for imaging viscosity variation in liver injury.</description><subject>Bioimaging</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fluorescent probe</subject><subject>HeLa Cells</subject><subject>Hep G2 Cells</subject><subject>Humans</subject><subject>Liver</subject><subject>Liver diseases</subject><subject>Lysosomes</subject><subject>Lysosomes - chemistry</subject><subject>Viscosity</subject><issn>0039-9140</issn><issn>1873-3573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEFvEzEQhS0EomnhJ4B85LLB9qx31yeEWiiVKpAQnC3HO1scbezi8Qbl3-OQwJWTNdab9958jL2SYi2F7N5u18XNLha3VkK1a6n0oPQTtpJDDw3oHp6ylRBgGiNbccEuibZCCAUCnrMLGFrZQy9XjG4CEfoS4gOfD5Qo7dzM94F8olAOfJoXXxZXQorEQ-Rz2CP3OM_EXRz_jJmX6rEg8V-h_KjfVfeAMaSF-Oe7r0eLlJE8xsIfc9rgC_ZscjPhy_N7xb5__PDt-lNz_-X27vr9feNBQmkkdKA0qt5M2IPfgIGxm_QwGYOy86NuETqjAHw_DVpsXGdAmlH1A6ipxQ6u2JuTb039WfsVu6t31e4uYi1nlQFou1botkr1SepzIso42cccdi4frBT2yNtu7Zm3PfK2J9517_U5YtnscPy39RdwFbw7CbAeug-YLfmA0eMYcsVuxxT-E_EbclGVYw</recordid><startdate>20240515</startdate><enddate>20240515</enddate><creator>Zhang, Yu</creator><creator>Jiang, Qingqing</creator><creator>Wang, Kai</creator><creator>Fang, Yuqi</creator><creator>Zhang, Peng</creator><creator>Wei, Liangchen</creator><creator>Li, Dongpeng</creator><creator>Shu, Wei</creator><creator>Xiao, Haibin</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4888-5181</orcidid></search><sort><creationdate>20240515</creationdate><title>Dissecting lysosomal viscosity fluctuations in live cells and liver tissues with an ingenious NIR fluorescent probe</title><author>Zhang, Yu ; Jiang, Qingqing ; Wang, Kai ; Fang, Yuqi ; Zhang, Peng ; Wei, Liangchen ; Li, Dongpeng ; Shu, Wei ; Xiao, Haibin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c313t-136325e279fe73cb393d6f58f99e16cd54e369233c7f850ba69319d27832f4e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Bioimaging</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fluorescent probe</topic><topic>HeLa Cells</topic><topic>Hep G2 Cells</topic><topic>Humans</topic><topic>Liver</topic><topic>Liver diseases</topic><topic>Lysosomes</topic><topic>Lysosomes - chemistry</topic><topic>Viscosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Jiang, Qingqing</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Fang, Yuqi</creatorcontrib><creatorcontrib>Zhang, Peng</creatorcontrib><creatorcontrib>Wei, Liangchen</creatorcontrib><creatorcontrib>Li, Dongpeng</creatorcontrib><creatorcontrib>Shu, Wei</creatorcontrib><creatorcontrib>Xiao, Haibin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Talanta (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Yu</au><au>Jiang, Qingqing</au><au>Wang, Kai</au><au>Fang, Yuqi</au><au>Zhang, Peng</au><au>Wei, Liangchen</au><au>Li, Dongpeng</au><au>Shu, Wei</au><au>Xiao, Haibin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dissecting lysosomal viscosity fluctuations in live cells and liver tissues with an ingenious NIR fluorescent probe</atitle><jtitle>Talanta (Oxford)</jtitle><addtitle>Talanta</addtitle><date>2024-05-15</date><risdate>2024</risdate><volume>272</volume><spage>125825</spage><epage>125825</epage><pages>125825-125825</pages><artnum>125825</artnum><issn>0039-9140</issn><eissn>1873-3573</eissn><abstract>Viscosity is a pivotal component in the cell microenvironment, while lysosomal viscosity fluctuation is associated with various human diseases, such as tumors and liver diseases. Herein, a near-infrared fluorescent probe (BIMM) based on merocyanine dyes was designed and synthesized for detecting lysosomal viscosity in live cells and liver tissue. The increase in viscosity restricts the free rotation of single bonds, leading to enhanced fluorescence intensity. BIMM exhibits high sensitivity and good selectivity, and is applicable to a wide pH range. BIMM has near-infrared emission, and the fluorescent intensity shows an excellent linear relationship with viscosity. Furthermore, BIMM possessing excellent lysosomes-targeting ability, and can monitor viscosity changes in live cells stimulated by dexamethasone, lipopolysaccharide (LPS), and nigericin, and differentiate between cancer cells and normal cells. Noticeably, BIMM can accurately analyze viscosity changes in various liver disease models with HepG2 cells, and is successfully utilized to visualize variations in viscosity on APAP-induced liver injury. All the results demonstrated that BIMM is a powerful wash-free tool to monitor the viscosity fluctuations in living systems.
[Display omitted]
•An ingenious near-infrared fluorescent probe (BIMM) for sensitively detecting viscosity was reported.•BIMM could effectively target lysosomes and observe changes of lysosomal viscosity in living cells.•BIMM could differentiate between cancer cells and normal cells.•BIMM was successfully used for imaging viscosity variation in liver injury.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38417371</pmid><doi>10.1016/j.talanta.2024.125825</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-4888-5181</orcidid></addata></record> |
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subjects | Bioimaging Fluorescent Dyes - chemistry Fluorescent probe HeLa Cells Hep G2 Cells Humans Liver Liver diseases Lysosomes Lysosomes - chemistry Viscosity |
title | Dissecting lysosomal viscosity fluctuations in live cells and liver tissues with an ingenious NIR fluorescent probe |
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