ALFY localizes to early endosomes and cellular protrusions to facilitate directional cell migration.
Kristiane SørengSerhiy PankivCamilla BergsmarkEllen M HaugstenAnette K DahlLaura R de la BallinaAi YamamotoAlf H LystadAnne SimonsenPublished in: Journal of cell science (2022)
Cell migration is a complex process underlying physiological and pathological processes such as brain development and cancer metastasis. The autophagy-linked FYVE protein (ALFY; also known as WDFY3), an autophagy adaptor protein known to promote clearance of protein aggregates, has been implicated in brain development and neural migration during cerebral cortical neurogenesis in mice. However, a specific role of ALFY in cell motility and extracellular matrix adhesion during migration has not been investigated. Here, we reveal a novel role for ALFY in the endocytic pathway and in cell migration. We show that ALFY localizes to RAB5- and EEA1-positive early endosomes in a PtdIns(3)P-dependent manner and is highly enriched in cellular protrusions at the leading and lagging edge of migrating cells. We find that cells lacking ALFY have reduced attachment and altered protein levels and glycosylation of integrins, resulting in the inability to form a proper leading edge and loss of directional cell motility.
Keyphrases
- cell migration
- induced apoptosis
- extracellular matrix
- single cell
- protein protein
- endoplasmic reticulum stress
- cell death
- cell cycle arrest
- signaling pathway
- oxidative stress
- binding protein
- cerebral ischemia
- amino acid
- biofilm formation
- stem cells
- resting state
- genome wide
- young adults
- mesenchymal stem cells
- escherichia coli
- metabolic syndrome
- gene expression
- squamous cell carcinoma
- blood brain barrier
- cell proliferation
- pseudomonas aeruginosa
- papillary thyroid
- multiple sclerosis
- brain injury
- bone marrow
- pi k akt
- high fat diet induced
- neural stem cells
- atomic force microscopy
- lymph node metastasis
- insulin resistance