COUP‐TFII plays a role in cAMP‐induced Schwann cell differentiation and in vitro myelination by up‐regulating Krox20

Abstract

AbstractSchwann cells (SCs) are known to produce myelin for saltatory nerve conduction in the peripheral nervous system (PNS). Schwann cell differentiation and myelination processes are controlled by several transcription factors including Sox10, Oct6/Pou3f1, and Krox20/Egr2. Chicken ovalbumin upstream promoter‐transcription factor II (COUP‐TFII/NR2F2) is an orphan receptor that plays a role in the development and differentiation. However, the role of COUP‐TFII in the transcriptional regulatory network of SC differentiation has not been fully identified yet. Thus, the objective of this study was to investigate the role and molecular hierarchy of COUP‐TFII during cAMP‐induced SC differentiation. Our results showed that dibutyryl‐cAMP (db‐cAMP) increased expression levels of COUP‐TFII along with the expressions of Oct6, Krox20, and myelin‐related genes known to be related to SC differentiation. Our mechanistic studies showed that COUP‐TFII acted downstream of Hsp90/ErbB2/Gab1/ERK‐AKT pathway during db‐cAMP‐induced SC differentiation. In addition, we found that COUP‐TFII induced Krox20 expression by directly binding to Krox20‐MSE8 as revealed by chromatin immunoprecipitation assay and promoter activity assay. In line with this, the expression of COUP‐TFII was increased before up‐regulation of Oct6, Krox20, and myelin‐related genes in the sciatic nerves during early postnatal myelination period. Finally, COUP‐TFII knockdown by COUP‐TFII siRNA or via AAV‐COUP‐TFII shRNA in SCs inhibited db‐cAMP‐induced SC differentiation and in vitro myelination of sensory axons, respectively. Taken together, these findings indicate that COUP‐TFII might be involved in postnatal myelination through induction of Krox20 in SCs. Our results present a new insight into the transcriptional regulatory mechanism in SC differentiation and myelination.image