Signaling through the epidermal growth factor receptor (EGFR) has critical roles in development and in diseases such as cancer. All ligands of the EGFR are made as membrane-anchored precursors whose ectodomain must be proteolytically released or """"""""shed"""""""" to trigger EGFR-signaling. EGFR-ligand shedding is therefore crucial for EGFR- signaling. The membrane-anchored metalloproteinase ADAM17 has emerged as the principal regulator of the bioavailability of EGFR-ligands. Mice lacking ADAM17 phenotypically resemble those lacking the EGFR, providing unequivocal genetic evidence for the essential role of ADAM17 in EGFR signaling and establishing ADAM17 as an important potential target for the treatment of EGFR-dependent cancers. ADAM17 activity is highly regulated and is influenced by numerous signaling pathways. How these pathways functionally intersect with ADAM17 and how ADAM17 is activated are key questions that are the subject of this application. Our results show that a mutant of ADAM17 that lacks its cytoplasmic domain and therefore has no potential phosphorylation sites, responds normally to all physiological stimuli of ectodomain shedding tested to date. Moreover, substitution of the ADAM17 transmembrane domain (TMD) domain with that from other integral membrane proteins abolished ADAM17 activation. This points to a novel mechanism of ADAM17 regulation via its TMD. We hypothesize that the ADAM17 TMD integrates and interprets signals that drive ADAM activation and is the critical regulatory entity mediating the regulation of EGFR-ligand shedding by ADAM17.
Aim 1 is focused on defining the role of the TMD in activating ADAM17 through structure/function studies. The main goal of aim 2 is to define the major signaling effectors that activate ADAM17 via its TMD by combining inhibition experiments using pharmacological compounds and siRNA technology with activation of signaling pathways by forced expression of relevant signaling molecules. The experiments in aim 3 will rigorously test the role of the ADAM17 cytoplasmic domain in EGFR signaling in vivo in a new knock-in mouse model lacking the ADAM17 cytoplasmic domain. Together, these aims will resolve the most pressing current questions regarding the regulation of ADAM17, a major cellular sheddase that is a critical molecule in EGFR signaling and a target for treatment of cancer.

Public Health Relevance

All ligands of the EGFR, a tyrosine kinase receptor with important roles in development and diseases such as cancer, must be proteolytically released to trigger EGFR- signaling. This proposal is focused on the principal metalloproteinase responsible for EGFR-ligand activation, ADAM17 (a disintegrin and metalloproteinase 17), and on understanding its regulation and function in the context of EGFR-signaling using cel- based assays and genetically modified mice.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM064750-13
Application #
8664870
Study Section
Molecular and Integrative Signal Transduction Study Section (MIST)
Program Officer
Nie, Zhongzhen
Project Start
2002-02-01
Project End
2015-05-31
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
13
Fiscal Year
2014
Total Cost
$351,000
Indirect Cost
$151,000
Name
Hospital for Special Surgery
Department
Type
DUNS #
622146454
City
New York
State
NY
Country
United States
Zip Code
10021
Qing, Xiaoping; Chinenov, Yurii; Redecha, Patricia et al. (2018) iRhom2 promotes lupus nephritis through TNF-? and EGFR signaling. J Clin Invest 128:1397-1412
Schaal, Justin B; Maretzky, Thorsten; Tran, Dat Q et al. (2018) Macrocyclic ?-defensins suppress tumor necrosis factor-? (TNF-?) shedding by inhibition of TNF-?-converting enzyme. J Biol Chem 293:2725-2734
Urriola-Muñoz, Paulina; Li, Xue; Maretzky, Thorsten et al. (2018) The xenoestrogens biphenol-A and nonylphenol differentially regulate metalloprotease-mediated shedding of EGFR ligands. J Cell Physiol 233:2247-2256
Brummer, Tobias; Pigoni, Martina; Rossello, Armando et al. (2018) The metalloprotease ADAM10 (a disintegrin and metalloprotease 10) undergoes rapid, postlysis autocatalytic degradation. FASEB J 32:3560-3573
Farber, Gregory; Hurtado, Romulo; Loh, Sarah et al. (2018) Glomerular endothelial cell maturation depends on ADAM10, a key regulator of Notch signaling. Angiogenesis 21:335-347
Farber, Gregory; Parks, Matthew M; Lustgarten Guahmich, Nicole et al. (2018) ADAM10 controls the differentiation of the coronary arterial endothelium. Angiogenesis :
Shipman, William D; Chyou, Susan; Ramanathan, Anusha et al. (2018) A protective Langerhans cell-keratinocyte axis that is dysfunctional in photosensitivity. Sci Transl Med 10:
Li, Xue; Maretzky, Thorsten; Perez-Aguilar, Jose Manuel et al. (2017) Structural modeling defines transmembrane residues in ADAM17 that are crucial for Rhbdf2-ADAM17-dependent proteolysis. J Cell Sci 130:868-878
Alabi, Rolake O; Glomski, Krzysztof; Haxaire, Coline et al. (2016) ADAM10-Dependent Signaling Through Notch1 and Notch4 Controls Development of Organ-Specific Vascular Beds. Circ Res 119:519-31
Qing, Xiaoping; Rogers, Lindsay; Mortha, Arthur et al. (2016) iRhom2 regulates CSF1R cell surface expression and non-steady state myelopoiesis in mice. Eur J Immunol 46:2737-2748

Showing the most recent 10 out of 58 publications