Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Plasma membrane-derived extracellular microvesicles mediate non-canonical intercellular NOTCH signaling
by
Wang, Qiyu
, Lu, Quan
in
631/1647/2067
/ 631/80/313
/ 631/80/86/820
/ Amyloid Precursor Protein Secretases - metabolism
/ Arrestin
/ Arrestin - metabolism
/ Cell Line, Tumor
/ Cell Membrane - ultrastructure
/ Extracellular Vesicles - physiology
/ Gene expression
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Membrane proteins
/ Membrane Proteins - metabolism
/ Metalloproteinase
/ multidisciplinary
/ Notch protein
/ Notch2 protein
/ Plasmas (physics)
/ Protein Transport
/ Proteins
/ Proteomics
/ Receptor, Notch2 - metabolism
/ Receptors
/ Receptors, Notch - physiology
/ Science
/ Science (multidisciplinary)
/ Secretase
/ Signal Transduction
/ Ubiquitin-protein ligase
/ Ubiquitin-Protein Ligases - metabolism
/ Vesicles
2017
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Plasma membrane-derived extracellular microvesicles mediate non-canonical intercellular NOTCH signaling
by
Wang, Qiyu
, Lu, Quan
in
631/1647/2067
/ 631/80/313
/ 631/80/86/820
/ Amyloid Precursor Protein Secretases - metabolism
/ Arrestin
/ Arrestin - metabolism
/ Cell Line, Tumor
/ Cell Membrane - ultrastructure
/ Extracellular Vesicles - physiology
/ Gene expression
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Membrane proteins
/ Membrane Proteins - metabolism
/ Metalloproteinase
/ multidisciplinary
/ Notch protein
/ Notch2 protein
/ Plasmas (physics)
/ Protein Transport
/ Proteins
/ Proteomics
/ Receptor, Notch2 - metabolism
/ Receptors
/ Receptors, Notch - physiology
/ Science
/ Science (multidisciplinary)
/ Secretase
/ Signal Transduction
/ Ubiquitin-protein ligase
/ Ubiquitin-Protein Ligases - metabolism
/ Vesicles
2017
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Plasma membrane-derived extracellular microvesicles mediate non-canonical intercellular NOTCH signaling
by
Wang, Qiyu
, Lu, Quan
in
631/1647/2067
/ 631/80/313
/ 631/80/86/820
/ Amyloid Precursor Protein Secretases - metabolism
/ Arrestin
/ Arrestin - metabolism
/ Cell Line, Tumor
/ Cell Membrane - ultrastructure
/ Extracellular Vesicles - physiology
/ Gene expression
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Membrane proteins
/ Membrane Proteins - metabolism
/ Metalloproteinase
/ multidisciplinary
/ Notch protein
/ Notch2 protein
/ Plasmas (physics)
/ Protein Transport
/ Proteins
/ Proteomics
/ Receptor, Notch2 - metabolism
/ Receptors
/ Receptors, Notch - physiology
/ Science
/ Science (multidisciplinary)
/ Secretase
/ Signal Transduction
/ Ubiquitin-protein ligase
/ Ubiquitin-Protein Ligases - metabolism
/ Vesicles
2017
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Plasma membrane-derived extracellular microvesicles mediate non-canonical intercellular NOTCH signaling
Journal Article
Plasma membrane-derived extracellular microvesicles mediate non-canonical intercellular NOTCH signaling
2017
Request Book From Autostore
and Choose the Collection Method
Overview
ARMMs (arrestin domain-containing protein 1 (ARRDC1)-mediated microvesicles) are extracellular vesicles that bud directly at the plasma membrane; however, little is known about the molecular composition and physiological function of these vesicles. Here we report that ARMMs contain active NOTCH receptors and mediate a non-canonical intercellular NOTCH signaling. We identify over 100 proteins that are significantly enriched in ARMMs, including ARRDC1, TSG101 and multiple ESCRT complex proteins. About a third of ARMMs-enriched proteins are plasma membrane proteins, including the NOTCH2 receptor. The incorporation of NOTCH2 into ARMMs is facilitated by the ITCH E3 ligase and the metalloprotease ADAM10, both of which are also secreted into ARMMs. NOTCH2 in ARMMs can be delivered into recipient cells, and upon activation by γ-secretase cleavage, induces NOTCH-specific gene expression. Together, our findings reveal a role for ARMMs in a novel NOTCH signaling pathway that acts in distance and is independent of direct cell–cell contact.
ARMMs are extracellular vesicles that bud directly at the plasma membrane; their function is poorly understood. Here the authors purify and carryout a proteomics analysis of the protein components of ARMMs, and show that NOTCH receptors are recruited into ARMMs and can be transferred to recipient cells to mediate NOTCH signaling.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ Amyloid Precursor Protein Secretases - metabolism
/ Arrestin
/ Cell Membrane - ultrastructure
/ Extracellular Vesicles - physiology
/ Humanities and Social Sciences
/ Humans
/ Membrane Proteins - metabolism
/ Proteins
/ Receptor, Notch2 - metabolism
/ Receptors, Notch - physiology
/ Science
/ Ubiquitin-Protein Ligases - metabolism
/ Vesicles
This website uses cookies to ensure you get the best experience on our website.