Suppression of PI3K signaling is linked to autophagy activation and the spatiotemporal induction of the lens organelle free zone
The terminal steps of lens cell differentiation require elimination of all organelles to create a central Organelle Free Zone (OFZ) that is required for lens function of focusing images on the retina. Previous studies show that the spatiotemporal elimination of these organelles during development is...
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Published in | Experimental cell research Vol. 412; no. 2; p. 113043 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
15.03.2022
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Online Access | Get full text |
ISSN | 0014-4827 1090-2422 1090-2422 |
DOI | 10.1016/j.yexcr.2022.113043 |
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Abstract | The terminal steps of lens cell differentiation require elimination of all organelles to create a central Organelle Free Zone (OFZ) that is required for lens function of focusing images on the retina. Previous studies show that the spatiotemporal elimination of these organelles during development is autophagy-dependent. We now show that the inhibition of PI3K signaling in lens organ culture results in the premature induction of autophagy within 24 h, including a significant increase in LAMP1+ lysosomes, and the removal of lens organelles from the center of the lens. Specific inhibition of just the PI3K/Akt signaling axis was directly linked to the elimination of mitochondria and ER, while pan-PI3K inhibitors that block all PI3K downstream signaling removed all organelles, including nuclei. Therefore, blocking the PI3K/Akt pathway was alone insufficient to remove nuclei. RNAseq analysis revealed increased mRNA levels of the endogenous inhibitor of PI3K activation, PIK3IP1, in differentiating lens fiber cells preceding the induction of OFZ formation. Co-immunoprecipitation confirmed that PIK3IP1 associates with multiple PI3K p110 isoforms just prior to formation of the OFZ, providing a likely endogenous mechanism for blocking all PI3K signaling and activating the autophagy pathway required to form the OFZ during lens development.
•PI3K inhibition is linked to spatiotemporal autophagy induction in embryonic lenses.•PI3K inhibition induces premature formation of the lens Organelle Free Zone (OFZ).•Suppression of the PI3K/Akt axis induces mitochondria and ER loss in OFZ formation.•Blocking Akt is alone insufficient to induce nuclear elimination in OFZ formation. |
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AbstractList | The terminal steps of lens cell differentiation require elimination of all organelles to create a central Organelle Free Zone (OFZ) that is required for lens function of focusing images on the retina. Previous studies show that the spatiotemporal elimination of these organelles during development is autophagy-dependent. We now show that the inhibition of PI3K signaling in lens organ culture results in the premature induction of autophagy within 24 h, including a significant increase in LAMP1+ lysosomes, and the removal of lens organelles from the center of the lens. Specific inhibition of just the PI3K/Akt signaling axis was directly linked to the elimination of mitochondria and ER, while pan-PI3K inhibitors that block all PI3K downstream signaling removed all organelles, including nuclei. Therefore, blocking the PI3K/Akt pathway was alone insufficient to remove nuclei. RNAseq analysis revealed increased mRNA levels of the endogenous inhibitor of PI3K activation, PIK3IP1, in differentiating lens fiber cells preceding the induction of OFZ formation. Co-immunoprecipitation confirmed that PIK3IP1 associates with multiple PI3K p110 isoforms just prior to formation of the OFZ, providing a likely endogenous mechanism for blocking all PI3K signaling and activating the autophagy pathway required to form the OFZ during lens development.The terminal steps of lens cell differentiation require elimination of all organelles to create a central Organelle Free Zone (OFZ) that is required for lens function of focusing images on the retina. Previous studies show that the spatiotemporal elimination of these organelles during development is autophagy-dependent. We now show that the inhibition of PI3K signaling in lens organ culture results in the premature induction of autophagy within 24 h, including a significant increase in LAMP1+ lysosomes, and the removal of lens organelles from the center of the lens. Specific inhibition of just the PI3K/Akt signaling axis was directly linked to the elimination of mitochondria and ER, while pan-PI3K inhibitors that block all PI3K downstream signaling removed all organelles, including nuclei. Therefore, blocking the PI3K/Akt pathway was alone insufficient to remove nuclei. RNAseq analysis revealed increased mRNA levels of the endogenous inhibitor of PI3K activation, PIK3IP1, in differentiating lens fiber cells preceding the induction of OFZ formation. Co-immunoprecipitation confirmed that PIK3IP1 associates with multiple PI3K p110 isoforms just prior to formation of the OFZ, providing a likely endogenous mechanism for blocking all PI3K signaling and activating the autophagy pathway required to form the OFZ during lens development. The terminal steps of lens cell differentiation require elimination of all organelles to create a central Organelle Free Zone (OFZ) that is required for lens function of focusing images on the retina. Previous studies show that the spatiotemporal elimination of these organelles during development is autophagy-dependent. We now show that the inhibition of PI3K signaling in lens organ culture results in the premature induction of autophagy within 24 hours, including a significant increase in LAMP1+ lysosomes, and the removal of lens organelles from the center of the lens. Specific inhibition of just the PI3K/Akt signaling axis was directly linked to the elimination of mitochondria and ER, while pan-PI3K inhibitors that block all PI3K downstream signaling removed all organelles, including nuclei. Therefore, blocking the PI3K/Akt pathway was alone insufficient to remove nuclei. RNAseq analysis revealed increased mRNA levels of the endogenous inhibitor of PI3K activation, PIK3IP1, in differentiating lens fiber cells preceding the induction of OFZ formation. Co-immunoprecipitation confirmed that PIK3IP1 associates with multiple PI3K p110 isoforms just prior to formation of the OFZ, providing a likely endogenous mechanism for blocking all PI3K signaling and activating the autophagy pathway required to form the OFZ during lens development. The terminal steps of lens cell differentiation require elimination of all organelles to create a central Organelle Free Zone (OFZ) that is required for lens function of focusing images on the retina. Previous studies show that the spatiotemporal elimination of these organelles during development is autophagy-dependent. We now show that the inhibition of PI3K signaling in lens organ culture results in the premature induction of autophagy within 24 h, including a significant increase in LAMP1+ lysosomes, and the removal of lens organelles from the center of the lens. Specific inhibition of just the PI3K/Akt signaling axis was directly linked to the elimination of mitochondria and ER, while pan-PI3K inhibitors that block all PI3K downstream signaling removed all organelles, including nuclei. Therefore, blocking the PI3K/Akt pathway was alone insufficient to remove nuclei. RNAseq analysis revealed increased mRNA levels of the endogenous inhibitor of PI3K activation, PIK3IP1, in differentiating lens fiber cells preceding the induction of OFZ formation. Co-immunoprecipitation confirmed that PIK3IP1 associates with multiple PI3K p110 isoforms just prior to formation of the OFZ, providing a likely endogenous mechanism for blocking all PI3K signaling and activating the autophagy pathway required to form the OFZ during lens development. The terminal steps of lens cell differentiation require elimination of all organelles to create a central Organelle Free Zone (OFZ) that is required for lens function of focusing images on the retina. Previous studies show that the spatiotemporal elimination of these organelles during development is autophagy-dependent. We now show that the inhibition of PI3K signaling in lens organ culture results in the premature induction of autophagy within 24 h, including a significant increase in LAMP1+ lysosomes, and the removal of lens organelles from the center of the lens. Specific inhibition of just the PI3K/Akt signaling axis was directly linked to the elimination of mitochondria and ER, while pan-PI3K inhibitors that block all PI3K downstream signaling removed all organelles, including nuclei. Therefore, blocking the PI3K/Akt pathway was alone insufficient to remove nuclei. RNAseq analysis revealed increased mRNA levels of the endogenous inhibitor of PI3K activation, PIK3IP1, in differentiating lens fiber cells preceding the induction of OFZ formation. Co-immunoprecipitation confirmed that PIK3IP1 associates with multiple PI3K p110 isoforms just prior to formation of the OFZ, providing a likely endogenous mechanism for blocking all PI3K signaling and activating the autophagy pathway required to form the OFZ during lens development. •PI3K inhibition is linked to spatiotemporal autophagy induction in embryonic lenses.•PI3K inhibition induces premature formation of the lens Organelle Free Zone (OFZ).•Suppression of the PI3K/Akt axis induces mitochondria and ER loss in OFZ formation.•Blocking Akt is alone insufficient to induce nuclear elimination in OFZ formation. |
ArticleNumber | 113043 |
Author | Gheyas, Rifah Chauss, Daniel Kantorow, Marc Ortega-Alvarez, Ramon Menko, A. Sue |
AuthorAffiliation | 2 Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL 1 Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35101390$$D View this record in MEDLINE/PubMed |
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Keywords | Organelle free zone (OFZ) p-p70S6K DMSO LC3B R123 JNK pmTOR RTK FP Autophagy TUNEL PI3K Development mTOR EC OFZ pJNK pRAPTOR Akt EQ ER RAPTOR PIK3IP1 GPCR Lens mTORC1 FC P70S6K |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 A.S.M. – Conceptualization, Funding acquisition, Methodology, Project Administration, Supervision, Writing-original draft; R.G. – Data curation, Formal analysis, Investigation, Validation, Visualization, Writing-original draft; M.K. – Funding acquisition, Methodology, Writing-review & editing; R.O-A. – Data curation, Investigation; D.C. – Data curation, Formal analysis, Investigation, Writing-review & editing AUTHOR CONTRIBUTIONS present address: Immunoregulation Section, Kidney Diseases Branch, NIDDK, NIH, Bethesda, MD |
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SubjectTerms | Akt Animals Autophagy Autophagy - physiology Cell Differentiation - physiology Cell Nucleus - metabolism Cell Nucleus - physiology Chick Embryo Development Epithelial Cells - metabolism Epithelial Cells - physiology Eye - metabolism Eye - physiopathology Lens Lens, Crystalline - metabolism Lens, Crystalline - physiology Mitochondria - metabolism Mitochondria - physiology Organelle free zone (OFZ) Phosphatidylinositol 3-Kinases - metabolism PI3K Proto-Oncogene Proteins c-akt - metabolism Signal Transduction - physiology |
Title | Suppression of PI3K signaling is linked to autophagy activation and the spatiotemporal induction of the lens organelle free zone |
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