AI Article Synopsis

  • The study confirms that NEUROD1 can successfully reprogram reactive astrocytes into neurons in vitro at an efficiency of 13.4%.
  • It identifies a total of 1952 proteins, with 92 exhibiting differential expression, highlighting 11 candidate proteins linked to the reprogramming process.
  • The NEUROD1-CSNK2A2-PNN pathway plays a crucial role in the conversion, as indicated by increased expression levels of CSNK2A2 and PNN in the reprogrammed astrocytes.

Article Abstract

Our previous study has confirmed that astrocytes overexpressing neurogenic differentiation factor 1 (NEUROD1) in the spinal cord can be reprogrammed into neurons under in vivo conditions. However, whether they can also be reprogrammed into neurons under in vitro conditions remains unclear, and the mechanisms of programmed conversion from astrocytes to neurons have not yet been clarified. In the present study, we prepared reactive astrocytes from newborn rat spinal cord astrocytes using the scratch method and infected them with lentivirus carrying NEUROD1. The results showed that NEUROD1 overexpression reprogrammed the cultured reactive astrocytes into neurons in vitro with an efficiency of 13.4%. Using proteomic and bioinformatic analyses, 1952 proteins were identified, of which 92 were differentially expressed. Among these proteins, 11 were identified as candidate proteins in the process of reprogramming based on their biological functions and fold-changes in the bioinformatic analysis. Furthermore, western blot assay revealed that casein kinase II subunit alpha (CSNK2A2) and pinin (PNN) expression in NEUROD1-overexpressing reactive astrocytes was significantly increased, suggesting that NEUROD1 can directly reprogram spinal cord-derived reactive astrocytes into neurons in vitro, and that the NEUROD1-CSNK2A2-PNN pathway is involved in this process. This study was approved by the Animal Ethics Committee of Fujian Medical University, China (approval No. 2016-05) on April 18, 2016.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354129PMC
http://dx.doi.org/10.4103/1673-5374.310697DOI Listing

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