Dynamin-Independent Mechanisms of Endocytosis and Receptor Trafficking

dc.contributor.authorGundu, Chayanika
dc.contributor.authorArruri, Vijay Kumar
dc.contributor.authorYadav, Poonam
dc.contributor.authorNavik, Umashanker
dc.contributor.authorKumar, Ashutosh
dc.contributor.authorAmalkar, Veda Sudhir
dc.contributor.authorVikram, Ajit
dc.contributor.authorGaddam, Ravinder Reddy
dc.date.accessioned2024-01-21T10:55:05Z
dc.date.accessioned2024-08-14T07:44:21Z
dc.date.available2024-01-21T10:55:05Z
dc.date.available2024-08-14T07:44:21Z
dc.date.issued2022-08-18T00:00:00
dc.description.abstractEndocytosis is a fundamental mechanism by which cells perform housekeeping functions. It occurs via a variety of mechanisms and involves many regulatory proteins. The GTPase dynamin acts as a �molecular scissor� to form endocytic vesicles and is a critical regulator among the proteins involved in endocytosis. Some GTPases (e.g., Cdc42, arf6, RhoA), membrane proteins (e.g., flotillins, tetraspanins), and secondary messengers (e.g., calcium) mediate dynamin-independent endocytosis. These pathways may be convergent, as multiple pathways exist in a single cell. However, what determines the specific path of endocytosis is complex and challenging to comprehend. This review summarizes the mechanisms of dynamin-independent endocytosis, the involvement of microRNAs, and factors that contribute to the cellular decision about the specific route of endocytosis. � 2022 by the authors.en_US
dc.identifier.doi10.3390/cells11162557
dc.identifier.issn20734409
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/4333
dc.identifier.urlhttps://www.mdpi.com/2073-4409/11/16/2557
dc.language.isoen_USen_US
dc.publisherMDPIen_US
dc.subjectcalciumen_US
dc.subjectdynaminen_US
dc.subjectendocytosisen_US
dc.subjectmicroRNAsen_US
dc.subjectnon-dynamin GTPasesen_US
dc.titleDynamin-Independent Mechanisms of Endocytosis and Receptor Traffickingen_US
dc.title.journalCellsen_US
dc.typeReviewen_US
dc.type.accesstypeOpen Accessen_US

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