Journal Article DZNE-2021-01394

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The pseudoprotease iRhom1 controls ectodomain shedding of membrane proteins in the nervous system.

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2021
Wiley Hoboken, NJ

The FASEB journal 35(11), e21962 () [10.1096/fj.202100936R]

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Abstract: Proteolytic ectodomain shedding of membrane proteins is a fundamental mechanism to control the communication between cells and their environment. A key protease for membrane protein shedding is ADAM17, which requires a non-proteolytic subunit, either inactive Rhomboid 1 (iRhom1) or iRhom2 for its activity. While iRhom1 and iRhom2 are co-expressed in most tissues and appear to have largely redundant functions, the brain is an organ with predominant expression of iRhom1. Yet, little is known about the spatio-temporal expression of iRhom1 in mammalian brain and about its function in controlling membrane protein shedding in the nervous system. Here, we demonstrate that iRhom1 is expressed in mouse brain from the prenatal stage to adulthood with a peak in early postnatal development. In the adult mouse brain iRhom1 was widely expressed, including in cortex, hippocampus, olfactory bulb, and cerebellum. Proteomic analysis of the secretome of primary neurons using the hiSPECS method and of cerebrospinal fluid, obtained from iRhom1-deficient and control mice, identified several membrane proteins that require iRhom1 for their shedding in vitro or in vivo. One of these proteins was 'multiple-EGF-like-domains protein 10' (MEGF10), a phagocytic receptor in the brain that is linked to the removal of amyloid β and apoptotic neurons. MEGF10 was further validated as an ADAM17 substrate using ADAM17-deficient mouse embryonic fibroblasts. Taken together, this study discovers a role for iRhom1 in controlling membrane protein shedding in the mouse brain, establishes MEGF10 as an iRhom1-dependent ADAM17 substrate and demonstrates that iRhom1 is widely expressed in murine brain.

Keyword(s): ADAM17 Protein: metabolism (MeSH) ; Animals (MeSH) ; Brain: metabolism (MeSH) ; Membrane Proteins: metabolism (MeSH) ; Membrane Proteins: physiology (MeSH) ; Mice (MeSH) ; Mice, Inbred C57BL (MeSH) ; Mice, Knockout (MeSH) ; Mouse Embryonic Stem Cells (MeSH) ; ADAM17 ; CSF ; hiSPECS ; iRhom1 ; myelination ; secretome ; Megf10 protein, mouse ; Membrane Proteins ; iRhom1 protein, mouse ; ADAM17 Protein ; Adam17 protein, mouse

Classification:

Contributing Institute(s):
  1. Neuroproteomics (AG Lichtenthaler)
  2. Molecular Neurobiology (AG Simons)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)
  2. 351 - Brain Function (POF4-351) (POF4-351)

Appears in the scientific report 2021
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Medline ; Creative Commons Attribution-NonCommercial CC BY-NC 4.0 ; OpenAccess ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Wiley ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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Institute Collections > M DZNE > M DZNE-AG Lichtenthaler
Document types > Articles > Journal Article
Institute Collections > M DZNE > M DZNE-AG Simons
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 Record created 2021-11-18, last modified 2023-09-15


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