Newt-derived extracellular vesicles promote mammalian nerve growth

Author:

Middleton Ryan1,Liao Ke1,Liu Weixin1,de Couto Geoff1,Garcia Nahuel2,Antes Travis1,Wang Yizhou3,Wu Di3,Li Xinling3,Tourtellotte Warren3,Marbán Eduardo1

Affiliation:

1. Cedars-Sinai Smidt Heart Institute

2. Gecorp

3. Cedars-Sinai Medical Center

Abstract

Abstract Newts have the extraordinary ability for regeneration, including the ability to regrow nerve and retinal tissue, and even amputated limbs. In contrast, mammals lack broad regenerative capabilities. While the molecular basis of newts’ regenerative ability is the subject of active study, the underlying paracrine signaling factors remain largely uncharacterized. Extracellular vesicles (EVs) play an important role in cell-to-cell communication via EV cargo-mediated regulation of gene expression patterns within the recipient cells. Here, we report that newt myogenic precursor cells (A1 cells) secrete EVs (A1EVs) that contain messenger RNAs associated with early embryonic development, neuronal differentiation, and cell survival. Exposure of rat primary superior cervical ganglion (SCG) neurons to A1EVs increased neurite outgrowth, facilitated by increases in mitochondrial respiration. Canonical pathway analysis pinpointed activation of NGF/ERK5 signaling in SCG neurons exposed to A1EV, which we validated experimentally. Thus, newt EVs drive mammalian neurite growth and complexity.

Publisher

Research Square Platform LLC

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