AI Article Synopsis

  • Membrane progesterone receptors (mPRs) were found in Schwann cells and may promote regeneration; this study explores their role in human adipose stem cells (ASC) converted to Schwann cell-like cells (SCL-ASC).
  • Both undifferentiated and differentiated ASCs expressed mPRs, with differentiation increasing mPR levels; activating mPRα enhanced cell movement, shape changes, and differentiation of SCL-ASC.
  • mPRα activation also boosted the expression and secretion of BDNF, a key growth factor for nerve healing, and was linked to the Src and PI3K-Akt signaling pathways, indicating mPRα's potential as a target for nerve regeneration therapies.

Article Abstract

Membrane progesterone receptors (mPRs) were recently found to be present and active in Schwann cells, where they have a potentially pro-regenerative activity. In this study, we investigated the role of mPRs in human adipose stem cells (ASC) differentiated into Schwann cell-like cells (SCL-ASC), which represent a promising alternative to Schwann cells for peripheral nerve regeneration. Our findings show that mPRs are present both in undifferentiated and differentiated ASC, and that the differentiation protocol upregulates mPR expression. Activation of mPRα promoted cell migration and differentiation in SCL-ASC, alongside with changes in cell morphology and mPRα localization. Moreover, it increased the expression and release of BDNF, a neurotrophin with pro-regenerative activity. Further analysis showed that Src and PI3K-Akt signaling pathways are involved in mPRα activity in SCL-ASC. These findings suggest that mPRα could play a pro-regenerative role in SCL-ASC and may be a promising target for the promotion of peripheral nerve regeneration.

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Source
http://dx.doi.org/10.1016/j.mce.2021.111298DOI Listing

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