Development of a Fluorescent Bodipy Probe for Visualization of the Serotonin 5-HT1A Receptor in Native Cells of the Immune System

dc.contributor.authorHernández Torres, Gloria
dc.contributor.authorEnríquez Palacios, Ernesto
dc.contributor.authorMecha Rodríguez, Miriam
dc.contributor.authorFeliú Martínez, Ana
dc.contributor.authorRueda Zubiaurre, Ainoa
dc.contributor.authorAngelina Querencias, Alba
dc.contributor.authorMartín-Fontecha Corrales, María Del Mar
dc.contributor.authorPalomares Gracia, Óscar
dc.contributor.authorGuaza Rodríguez, Carmen
dc.contributor.authorPeña Cabrera, Eduardo
dc.contributor.authorLópez Rodríguez, María Luz
dc.contributor.authorOrtega Gutiérrez, Silvia
dc.contributor.authorMartín De La Cruz, Leticia
dc.date.accessioned2023-06-17T12:28:23Z
dc.date.available2023-06-17T12:28:23Z
dc.date.issued2018-05-07
dc.descriptionThe Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.bioconjchem.8b00228. Received: March 30, 2018; Revised: May 4, 2018; Published: May 7, 2018
dc.description.abstractSerotonin (5-HT) modulates key aspects of the immune system. However, its precise function and the receptors involved in the observed effects have remained elusive. Among the different serotonin receptors, 5-HT1A plays an important role in the immune system given its presence in cells involved in both the innate and adaptive immune responses, but its actual levels of expression under different conditions have not been comprehensively studied due to the lack of suitable tools. To further clarify the role of 5-HT1A receptor in the immune system, we have developed a fluorescent small molecule probe that enables the direct study of the receptor levels in native cells. This probe allows direct profiling of the receptor expression in immune cells using flow cytometry. Our results show that important subsets of immune cells including human monocytes and dendritic cells express functional 5-HT1A and that its activation is associated with anti-inflammatory signaling. Furthermore, application of the probe to the experimental autoimmune encephalomyelitis model of multiple sclerosis demonstrates its potential to detect the specific overexpression of the 5-HT1A receptor in CD4+ T cells. Accordingly, the probe reported herein represents a useful tool whose use can be extended to study the levels of 5-HT1A receptor in ex vivo samples of different immune system conditions.
dc.description.departmentUnidad Docente de Bioquímica y Biología Molecular
dc.description.facultyFac. de Óptica y Optometría
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)
dc.description.sponsorshipRed Española de Esclerosis Múltiple
dc.description.sponsorshipCONACyT
dc.description.sponsorshipUniversidad Complutense de Madrid
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/48271
dc.identifier.doi10.1021/acs.bioconjchem.8b00228
dc.identifier.issn1043-1802
dc.identifier.officialurlhttp://dx.doi.org/10.1021/acs.bioconjchem.8b00228
dc.identifier.relatedurlhttps://pubs.acs.org/doi/pdfplus/10.1021/acs.bioconjchem.8b00228
dc.identifier.urihttps://hdl.handle.net/20.500.14352/12192
dc.issue.number6
dc.journal.titleBioconjugate Chemistry
dc.language.isoeng
dc.page.final2027
dc.page.initial2021
dc.publisherAmerican Chemical Society (ACS)
dc.relation.projectID(SAF2016-76449-R; SAF2016-78792-R; SAF2017-84978-R)
dc.relation.projectIDRD16/0015/0021
dc.relation.projectIDCB-253623
dc.relation.projectIDCB-123732
dc.rights.accessRightsrestricted access
dc.subject.cdu577.27
dc.subject.cdu612.822:616.832-004
dc.subject.cdu577.175.823
dc.subject.keywordFluorescent bodipy probe
dc.subject.keywordSerotonin
dc.subject.keyword5-HT1A
dc.subject.keywordinmune system
dc.subject.keywordMultiple sclerosis
dc.subject.keywordencpphelamyelitits
dc.subject.ucmBioquímica (Química)
dc.subject.ucmInmunología
dc.subject.unesco2412 Inmunología
dc.titleDevelopment of a Fluorescent Bodipy Probe for Visualization of the Serotonin 5-HT1A Receptor in Native Cells of the Immune System
dc.typejournal article
dc.volume.number29
dspace.entity.typePublication
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