Melanin transferred to keratinocytes resides in non-degradative endocytic compartments

Detalhes bibliográficos
Autor(a) principal: Correia, Maria S
Data de Publicação: 2018
Outros Autores: Moreiras, Hugo, Pereira, Francisco J C, Neto, Matilde V, Festas, Tiago C, Tarafder, Abul K, Ramalho, José S, Seabra, Miguel C, Barral, Duarte C
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/149314
Resumo: Funding: We thank the staff from the Unit of Imaging and Cytometry of the Instituto Gulbenkian de Ciência for assistance in microscopy and flow cytometry protocol adjustments, the CEDOC Microscopy Facility for assistance in image acquisition and analysis, Dot Bennett for the kind gift of cell lines, and Alistair Hume for the kind gift of anti-Rab5 antibody. This project was supported by Fundação para a Ciência e a Tecnologia (FCT), Portugal (PTDC/BIA-BCM/ 111735/2009, EXPL/BEX-BCM/0379/2013), MSC and HM were supported by FCT PhD studentships (SFRH/BD/65381/2009 and PD/BD/114118/2015, respectively), FJCP was supported by an FCT postdoctoral fellowship (SFRH/ BPD/70337/2010), and DCB was supported by the FCT Investigator Program (IF/00501/2014/CP1252/CT0001).
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spelling Melanin transferred to keratinocytes resides in non-degradative endocytic compartmentsLAMPlysosomal-associated membrane proteinPARPBSphosphate buffered salineprotease-activated receptorsiRNAsmall interfering RNAFunding: We thank the staff from the Unit of Imaging and Cytometry of the Instituto Gulbenkian de Ciência for assistance in microscopy and flow cytometry protocol adjustments, the CEDOC Microscopy Facility for assistance in image acquisition and analysis, Dot Bennett for the kind gift of cell lines, and Alistair Hume for the kind gift of anti-Rab5 antibody. This project was supported by Fundação para a Ciência e a Tecnologia (FCT), Portugal (PTDC/BIA-BCM/ 111735/2009, EXPL/BEX-BCM/0379/2013), MSC and HM were supported by FCT PhD studentships (SFRH/BD/65381/2009 and PD/BD/114118/2015, respectively), FJCP was supported by an FCT postdoctoral fellowship (SFRH/ BPD/70337/2010), and DCB was supported by the FCT Investigator Program (IF/00501/2014/CP1252/CT0001).Melanin transfer from melanocytes to keratinocytes and subsequent accumulation in the supra-nuclear region is a critical process in skin pigmentation and protection against ultraviolet radiation. We have previously proposed that the main mode of transfer between melanocytes and keratinocytes is through exo/endocytosis of the melanosome core, termed melanocore. In this study, we developed an in vitro uptake assay using melanocores secreted by melanocytes. We show that the uptake of melanocores, but not melanosomes, by keratinocytes is Protease-activated receptor (PAR)-2-dependent. Furthermore, we found that the silencing of the early endocytic regulator Rab5b, but not the late endocytic regulators Rab7a or Rab9a, significantly impairs melanocore uptake by keratinocytes. Following uptake, we observed that melanin accumulates in compartments that are positive for both early and late endocytic markers. We found that melanin does not localize to either highly degradative or acidic organelles, as assessed by LysoTracker and DQ-BSA staining, despite the abundance of these types of organelles within keratinocytes. Therefore, we propose that melanocore uptake leads to storage of melanin within keratinocytes in hybrid endocytic compartments that are not highly acidic or degradative. By avoiding lysosomal degradation, these specialized endosomes may allow melanin to persist within keratinocytes for long periods.NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)Centro de Estudos de Doenças Crónicas (CEDOC)RUNCorreia, Maria SMoreiras, HugoPereira, Francisco J CNeto, Matilde VFestas, Tiago CTarafder, Abul KRamalho, José SSeabra, Miguel CBarral, Duarte C2023-02-16T22:13:43Z2018-032018-03-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10application/pdfhttp://hdl.handle.net/10362/149314eng0022-202XPURE: 3278434https://doi.org/10.1016/j.jid.2017.09.042info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T05:31:15Zoai:run.unl.pt:10362/149314Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:53:42.936966Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Melanin transferred to keratinocytes resides in non-degradative endocytic compartments
title Melanin transferred to keratinocytes resides in non-degradative endocytic compartments
spellingShingle Melanin transferred to keratinocytes resides in non-degradative endocytic compartments
Correia, Maria S
LAMP
lysosomal-associated membrane protein
PAR
PBS
phosphate buffered saline
protease-activated receptor
siRNA
small interfering RNA
title_short Melanin transferred to keratinocytes resides in non-degradative endocytic compartments
title_full Melanin transferred to keratinocytes resides in non-degradative endocytic compartments
title_fullStr Melanin transferred to keratinocytes resides in non-degradative endocytic compartments
title_full_unstemmed Melanin transferred to keratinocytes resides in non-degradative endocytic compartments
title_sort Melanin transferred to keratinocytes resides in non-degradative endocytic compartments
author Correia, Maria S
author_facet Correia, Maria S
Moreiras, Hugo
Pereira, Francisco J C
Neto, Matilde V
Festas, Tiago C
Tarafder, Abul K
Ramalho, José S
Seabra, Miguel C
Barral, Duarte C
author_role author
author2 Moreiras, Hugo
Pereira, Francisco J C
Neto, Matilde V
Festas, Tiago C
Tarafder, Abul K
Ramalho, José S
Seabra, Miguel C
Barral, Duarte C
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)
Centro de Estudos de Doenças Crónicas (CEDOC)
RUN
dc.contributor.author.fl_str_mv Correia, Maria S
Moreiras, Hugo
Pereira, Francisco J C
Neto, Matilde V
Festas, Tiago C
Tarafder, Abul K
Ramalho, José S
Seabra, Miguel C
Barral, Duarte C
dc.subject.por.fl_str_mv LAMP
lysosomal-associated membrane protein
PAR
PBS
phosphate buffered saline
protease-activated receptor
siRNA
small interfering RNA
topic LAMP
lysosomal-associated membrane protein
PAR
PBS
phosphate buffered saline
protease-activated receptor
siRNA
small interfering RNA
description Funding: We thank the staff from the Unit of Imaging and Cytometry of the Instituto Gulbenkian de Ciência for assistance in microscopy and flow cytometry protocol adjustments, the CEDOC Microscopy Facility for assistance in image acquisition and analysis, Dot Bennett for the kind gift of cell lines, and Alistair Hume for the kind gift of anti-Rab5 antibody. This project was supported by Fundação para a Ciência e a Tecnologia (FCT), Portugal (PTDC/BIA-BCM/ 111735/2009, EXPL/BEX-BCM/0379/2013), MSC and HM were supported by FCT PhD studentships (SFRH/BD/65381/2009 and PD/BD/114118/2015, respectively), FJCP was supported by an FCT postdoctoral fellowship (SFRH/ BPD/70337/2010), and DCB was supported by the FCT Investigator Program (IF/00501/2014/CP1252/CT0001).
publishDate 2018
dc.date.none.fl_str_mv 2018-03
2018-03-01T00:00:00Z
2023-02-16T22:13:43Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10362/149314
url http://hdl.handle.net/10362/149314
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0022-202X
PURE: 3278434
https://doi.org/10.1016/j.jid.2017.09.042
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eu_rights_str_mv openAccess
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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