Caitlin M. Lange

ORCID: 0000-0003-4146-5288
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About
Contact & Profiles
Research Areas
  • Autophagy in Disease and Therapy
  • Genetics, Aging, and Longevity in Model Organisms
  • Endoplasmic Reticulum Stress and Disease
  • Aging, Elder Care, and Social Issues
  • Sirtuins and Resveratrol in Medicine

Sanford Burnham Prebys Medical Discovery Institute
2022-2024

Discovery Institute
2024

A decline in macroautophagic/autophagic activity with age contributes to the accumulation of damaged molecules and is associated impairment neuronal functions onset age-related diseases, particularly neurodegenerative disorders. To learn about neuronal-specific roles autophagy genes aging, we specifically inhibited pan-neuronally

10.1080/15548627.2024.2322420 article EN Autophagy 2024-02-27

ABSTRACT While autophagy is key to maintain cellular homeostasis, tissue-specific roles of individual genes are less understood. To study neuronal in vivo , we inhibited specifically C. elegans neurons, and unexpectedly found that knockdown early-acting genes, i.e., involved formation the autophagosome, except for atg-16.2 decreased PolyQ aggregates increased lifespan, albeit independently degradation autophagosomal cargo. Neuronal can be secreted from neurons via vesicles called exophers,...

10.1101/2022.12.12.520171 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2022-12-14

10.1016/j.cophys.2022.100591 article EN Current Opinion in Physiology 2022-09-26
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