Abstract

Embryonic Dissociated Dorsal Root Ganglia (DRG) cultures are often used to investigate the role of novel molecular pathways or drugs in Schwann cell development and myelination. These cultures largely recapitulate the order of cellular and molecular events that occur in Schwann cells of embryonic nerves. However, the timing of Schwann cell developmental transitions, notably the transition from Schwann Cell Precursors (SCP) to immature Schwann cells (iSC) and then to myelinating Schwann cells, has not been estimated so far in this culture system. In this study, we determined the expression profiles of Schwann cell developmental genes during the first week of culture and then compared our data to the expression profiles of these genes in developing spinal nerves. This helped in identifying that SCP transition into iSC between the 5th and 7th day in vitro. Furthermore, we also investigated the transition of immature cells into pro-myelinating and myelinating Schwann cells upon the induction of myelination in vitro. Our results suggest that Schwann cell differentiation beyond the immature stage can be observed as early as 4 days post the induction of myelination in cocultures. Finally, we compared the myelinating potential of coculture-derived Schwann cell monocultures to cultures established from neonatal sciatic nerves and found that both these culture systems exhibit similar myelinating phenotypes. In effect, our results allow for a better understanding and interpretation of coculture experiments especially in studies that aim to elucidate the role of a novel actor in Schwann cell development and myelination.

Highlights

  • Dissociated Dorsal Root Ganglia (DRG) cultures from mouse embryos have long been utilized as a resourceful model for exploring the nuances of Schwann cell development in vitro (Taveggia and Bolino, 2018)

  • We observed the presence of Oct6+ and Krox20+ Schwann cells located on top of the axons once the differentiation process is stimulated by Ascorbic Acid (AA) addition. These results show that SC at Days in vitro 7 (DIV7) differentiate into pro-myelinating Schwann cells (mSC) and mSC after AA supplementation which is comparable to the perinatal immature Schwann cells (iSC)/mSC transition in vivo

  • These results suggest that SC monocultures established from DIV7 cocultures are comparable to primary cultures established from neonatal sciatic nerves with regard to the change in SC phenotype upon cAMP addition. We observed that these monocultures do not express the Schwann Cell Precursors (SCP) marker Tfap2α at the protein level. These results provide further evidence that DIV7 SC are phenotypically different from SCP that arise in DRG/SC cocultures between DIV1 and DIV5 and they are rather similar to neonatal SC in culture

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Summary

Introduction

Dissociated Dorsal Root Ganglia (DRG) cultures from mouse embryos have long been utilized as a resourceful model for exploring the nuances of Schwann cell development in vitro (Taveggia and Bolino, 2018). The co-culture system provides a solid experimental framework to study different aspects of Schwann cell development such as proliferation, migration, differentiation, and myelination of axons (Päiväläinen et al, 2008; Taveggia and Bolino, 2018). It SCP/iSC/mSC Transition in DRG Cultures recapitulates the different aspects of Schwann cell development that are observed in vivo. It is well known that temporal differences exist between Schwann cell development in Dissociated DRG/SC coculture in vitro, and in developing spinal nerves in vivo. At around E15.5 in mice, SCPs undergo a transition into immature Schwann cells (iSC) that further differentiate into either myelinating or non-myelinating Schwann cells, perinatally (Monk et al, 2015; Fledrich et al, 2019; Jessen and Mirsky, 2019)

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