Building endocytic pits without clathrin.
Identifieur interne : 002D70 ( PubMed/Corpus ); précédent : 002D69; suivant : 002D71Building endocytic pits without clathrin.
Auteurs : Ludger Johannes ; Robert G. Parton ; Patricia Bassereau ; Satyajit MayorSource :
- Nature reviews. Molecular cell biology [ 1471-0080 ] ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Actins, Clathrin, Lectins.
- chemistry : Cell Membrane.
- metabolism : Cell Membrane.
- Animals, Endocytosis, Humans, Metabolic Networks and Pathways.
Abstract
How endocytic pits are built in clathrin- and caveolin-independent endocytosis still remains poorly understood. Recent insight suggests that different forms of clathrin-independent endocytosis might involve the actin-driven focusing of membrane constituents, the lectin-glycosphingolipid-dependent construction of endocytic nanoenvironments, and Bin-Amphiphysin-Rvs (BAR) domain proteins serving as scaffolding modules. We discuss the need for different types of internalization processes in the context of diverse cellular functions, the existence of clathrin-independent mechanisms of cargo recruitment and membrane bending from a biological and physical perspective, and finally propose a generic scheme for the formation of clathrin-independent endocytic pits.
DOI: 10.1038/nrm3968
PubMed: 25857812
Links to Exploration step
pubmed:25857812Le document en format XML
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Parton</name><affiliation><nlm:affiliation>University of Queensland, Institute for Molecular Bioscience and Centre for Microscopy and Microanalysis, St Lucia QLD 4072, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Bassereau, Patricia" sort="Bassereau, Patricia" uniqKey="Bassereau P" first="Patricia" last="Bassereau">Patricia Bassereau</name><affiliation><nlm:affiliation>Institut Curie, PSL Research University, Membrane and Cell Functions Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Centre National de la Recherche Scientifique UMR168, 75005 Paris, France; and Université Pierre et Marie Curie, 75252 Paris, France.</nlm:affiliation></affiliation></author><author><name sortKey="Mayor, Satyajit" sort="Mayor, Satyajit" uniqKey="Mayor S" first="Satyajit" last="Mayor">Satyajit Mayor</name><affiliation><nlm:affiliation>National Centre for Biological Sciences, Cellular Organization and Signaling Group, and at Institute for Stem Cell Biology and Regenerative Medicine, UAS-GKVK Campus, 560 065 Bangalore, India.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2015">2015</date><idno type="RBID">pubmed:25857812</idno><idno type="pmid">25857812</idno><idno type="doi">10.1038/nrm3968</idno><idno type="wicri:Area/PubMed/Corpus">002D70</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002D70</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Building endocytic pits without clathrin.</title><author><name sortKey="Johannes, Ludger" sort="Johannes, Ludger" uniqKey="Johannes L" first="Ludger" last="Johannes">Ludger Johannes</name><affiliation><nlm:affiliation>Institut Curie, PSL Research University, Endocytic Trafficking and Therapeutic Delivery Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Centre National de la Recherche Scientifique UMR3666, 75005 Paris, France; and INSERM U1143, 75005 Paris, France.</nlm:affiliation></affiliation></author><author><name sortKey="Parton, Robert G" sort="Parton, Robert G" uniqKey="Parton R" first="Robert G" last="Parton">Robert G. Parton</name><affiliation><nlm:affiliation>University of Queensland, Institute for Molecular Bioscience and Centre for Microscopy and Microanalysis, St Lucia QLD 4072, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Bassereau, Patricia" sort="Bassereau, Patricia" uniqKey="Bassereau P" first="Patricia" last="Bassereau">Patricia Bassereau</name><affiliation><nlm:affiliation>Institut Curie, PSL Research University, Membrane and Cell Functions Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Centre National de la Recherche Scientifique UMR168, 75005 Paris, France; and Université Pierre et Marie Curie, 75252 Paris, France.</nlm:affiliation></affiliation></author><author><name sortKey="Mayor, Satyajit" sort="Mayor, Satyajit" uniqKey="Mayor S" first="Satyajit" last="Mayor">Satyajit Mayor</name><affiliation><nlm:affiliation>National Centre for Biological Sciences, Cellular Organization and Signaling Group, and at Institute for Stem Cell Biology and Regenerative Medicine, UAS-GKVK Campus, 560 065 Bangalore, India.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Nature reviews. Molecular cell biology</title><idno type="eISSN">1471-0080</idno><imprint><date when="2015" type="published">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Actins (metabolism)</term><term>Animals</term><term>Cell Membrane (chemistry)</term><term>Cell Membrane (metabolism)</term><term>Clathrin (metabolism)</term><term>Endocytosis</term><term>Humans</term><term>Lectins (metabolism)</term><term>Metabolic Networks and Pathways</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Actins</term><term>Clathrin</term><term>Lectins</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Cell Membrane</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Cell Membrane</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Endocytosis</term><term>Humans</term><term>Metabolic Networks and Pathways</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">How endocytic pits are built in clathrin- and caveolin-independent endocytosis still remains poorly understood. Recent insight suggests that different forms of clathrin-independent endocytosis might involve the actin-driven focusing of membrane constituents, the lectin-glycosphingolipid-dependent construction of endocytic nanoenvironments, and Bin-Amphiphysin-Rvs (BAR) domain proteins serving as scaffolding modules. We discuss the need for different types of internalization processes in the context of diverse cellular functions, the existence of clathrin-independent mechanisms of cargo recruitment and membrane bending from a biological and physical perspective, and finally propose a generic scheme for the formation of clathrin-independent endocytic pits.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25857812</PMID><DateCreated><Year>2015</Year><Month>04</Month><Day>24</Day></DateCreated><DateCompleted><Year>2015</Year><Month>06</Month><Day>22</Day></DateCompleted><DateRevised><Year>2017</Year><Month>06</Month><Day>06</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1471-0080</ISSN><JournalIssue CitedMedium="Internet"><Volume>16</Volume><Issue>5</Issue><PubDate><Year>2015</Year><Month>05</Month></PubDate></JournalIssue><Title>Nature reviews. Molecular cell biology</Title><ISOAbbreviation>Nat. Rev. Mol. Cell Biol.</ISOAbbreviation></Journal><ArticleTitle>Building endocytic pits without clathrin.</ArticleTitle><Pagination><MedlinePgn>311-21</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1038/nrm3968</ELocationID><Abstract><AbstractText>How endocytic pits are built in clathrin- and caveolin-independent endocytosis still remains poorly understood. Recent insight suggests that different forms of clathrin-independent endocytosis might involve the actin-driven focusing of membrane constituents, the lectin-glycosphingolipid-dependent construction of endocytic nanoenvironments, and Bin-Amphiphysin-Rvs (BAR) domain proteins serving as scaffolding modules. We discuss the need for different types of internalization processes in the context of diverse cellular functions, the existence of clathrin-independent mechanisms of cargo recruitment and membrane bending from a biological and physical perspective, and finally propose a generic scheme for the formation of clathrin-independent endocytic pits.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Johannes</LastName><ForeName>Ludger</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Institut Curie, PSL Research University, Endocytic Trafficking and Therapeutic Delivery Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Centre National de la Recherche Scientifique UMR3666, 75005 Paris, France; and INSERM U1143, 75005 Paris, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Parton</LastName><ForeName>Robert G</ForeName><Initials>RG</Initials><AffiliationInfo><Affiliation>University of Queensland, Institute for Molecular Bioscience and Centre for Microscopy and Microanalysis, St Lucia QLD 4072, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Bassereau</LastName><ForeName>Patricia</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Institut Curie, PSL Research University, Membrane and Cell Functions Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Centre National de la Recherche Scientifique UMR168, 75005 Paris, France; and Université Pierre et Marie Curie, 75252 Paris, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mayor</LastName><ForeName>Satyajit</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>National Centre for Biological Sciences, Cellular Organization and Signaling Group, and at Institute for Stem Cell Biology and Regenerative Medicine, UAS-GKVK Campus, 560 065 Bangalore, India.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType 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