Adaptor Protein2 (AP2) Orchestrates CXCR2‐Mediated Cell Migration. (April 2014)
- Record Type:
- Journal Article
- Title:
- Adaptor Protein2 (AP2) Orchestrates CXCR2‐Mediated Cell Migration. (April 2014)
- Main Title:
- Adaptor Protein2 (AP2) Orchestrates CXCR2‐Mediated Cell Migration
- Authors:
- Raman, Dayanidhi
Sai, Jiqing
Hawkins, Oriana
Richmond, Ann - Abstract:
- <abstract abstract-type="main" id="tra12154-abs-0001"> <title>Abstract</title> <p id="tra12154-para-0001">The chemokine receptor CXCR2 is vital for inflammation, wound healing, angiogenesis, cancer progression and metastasis. Adaptor protein 2 (AP2), a clathrin binding heterotetrameric protein comprised of α, β2, μ2 and σ2 subunits, facilitates clathrin‐mediated endocytosis. Mutation of the LLKIL motif in the CXCR2 carboxyl‐terminal domain (CTD) results in loss of AP2 binding to the receptor and loss of ligand‐mediated receptor internalization and chemotaxis. AP2 knockdown also results in diminished ligand‐mediated CXCR2 internalization, polarization and chemotaxis. Using knockdown/rescue approaches with AP2‐μ2 mutants, the binding domains were characterized in reference to CXCR2 internalization and chemotaxis. When in an open conformation, μ2 Patch 1 and Patch 2 domains bind tightly to membrane PIP2 phospholipids. When AP2‐μ2, is replaced with μ2 mutated in Patch 1 and/or Patch 2 domains, ligand‐mediated receptor binding and internalization are not lost. However, chemotaxis requires AP2‐μ2 Patch 1, but not Patch 2. AP2‐σ2 has been demonstrated to bind dileucine motifs to facilitate internalization. Expression of AP2‐σ2 V88D and V98S dominant negative mutants resulted in loss of CXCR2 mediated chemotaxis. Thus, AP2 binding to both membrane phosphatidylinositol phospholipids and dileucine motifs is crucial for directional migration or chemotaxis. Moreover, AP2‐mediated<abstract abstract-type="main" id="tra12154-abs-0001"> <title>Abstract</title> <p id="tra12154-para-0001">The chemokine receptor CXCR2 is vital for inflammation, wound healing, angiogenesis, cancer progression and metastasis. Adaptor protein 2 (AP2), a clathrin binding heterotetrameric protein comprised of α, β2, μ2 and σ2 subunits, facilitates clathrin‐mediated endocytosis. Mutation of the LLKIL motif in the CXCR2 carboxyl‐terminal domain (CTD) results in loss of AP2 binding to the receptor and loss of ligand‐mediated receptor internalization and chemotaxis. AP2 knockdown also results in diminished ligand‐mediated CXCR2 internalization, polarization and chemotaxis. Using knockdown/rescue approaches with AP2‐μ2 mutants, the binding domains were characterized in reference to CXCR2 internalization and chemotaxis. When in an open conformation, μ2 Patch 1 and Patch 2 domains bind tightly to membrane PIP2 phospholipids. When AP2‐μ2, is replaced with μ2 mutated in Patch 1 and/or Patch 2 domains, ligand‐mediated receptor binding and internalization are not lost. However, chemotaxis requires AP2‐μ2 Patch 1, but not Patch 2. AP2‐σ2 has been demonstrated to bind dileucine motifs to facilitate internalization. Expression of AP2‐σ2 V88D and V98S dominant negative mutants resulted in loss of CXCR2 mediated chemotaxis. Thus, AP2 binding to both membrane phosphatidylinositol phospholipids and dileucine motifs is crucial for directional migration or chemotaxis. Moreover, AP2‐mediated receptor internalization can be dissociated from AP2‐mediated chemotaxis.</p> <p> <inline-graphic xlink:href="ark:/27927/pgg4swwqjsm" mimetype="image" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /> </p> </abstract> … (more)
- Is Part Of:
- Traffic. Volume 15:Number 4(2014:Apr.)
- Journal:
- Traffic
- Issue:
- Volume 15:Number 4(2014:Apr.)
- Issue Display:
- Volume 15, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 15
- Issue:
- 4
- Issue Sort Value:
- 2014-0015-0004-0000
- Page Start:
- 451
- Page End:
- 469
- Publication Date:
- 2014-04
- Subjects:
- Biological transport -- Periodicals
571.6 - Journal URLs:
- http://www.blackwell-synergy.com/Journals/member/institutions/issuelist.asp?journal=tra ↗
http://www.blackwellpublishing.com/journal.asp?ref=1398-9219&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-0854 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/tra.12154 ↗
- Languages:
- English
- ISSNs:
- 1398-9219
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8881.575000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3717.xml