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SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 60 (P60)

ABSTRACT: Single cell RNA sequencing of sorted mouse Schwann cells expressing eYFP due to P0Cre-mediated recombination.

ORGANISM(S): Mus musculus

PROVIDER: GSE138453 | GEO | 2021/04/22

REPOSITORIES: GEO

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SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 1 (P1)

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SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 5 (P5)

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SNAT - Single cell RNA sequencing of mouse cells sorted from sciatic nerves at postnatal day 1 (P1) and P60

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SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 60 (P60)

Project description:SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 60 (P60)

| PRJNA575892 | ENA

SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 1 (P1)

Project description:SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 1 (P1)

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SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 5 (P5)

Project description:SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 5 (P5)

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SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 14 (P14)

Project description:SNAT - Single cell RNA sequencing of mouse sorted Schwann cells at postnatal day 14 (P14)

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Functions of HDAC1 and HDAC2 in Schwann cells during postnatal

Project description:The aim of our study is to determine the functions of histone deacetylases (HDACs) 1 and 2 in Schwann cells during postnatal development of the peripheral nervous system (PNS). Schwann cells are the myelinating glial cells of the PNS. At birth, mouse sciatic nerves mature in 2 subsequent phases: 1/ big caliber axons get sorted into a 1 to 1 relationship with Schwann cells, 2/ Schwann cells build a myelin sheath around sorted axons. In mice where both HDAC1 & HDAC2 have been specifically knocked out in Schwann cells, both phases are impaired. HDACs are chromatin remodeling enzymes, they can thus alter gene expression directly. We want to identify which genes controlled by HDAC1 and HDAC2 in Schwann cells are necessary for the maturation of sciatic nerves. Because HDAC1 and HDAC2 can compensate for each other loss to some extend, we will first analyze changes of gene expression in HDAC1/HDAC2 double KO animals. We expect to gain critical insights into the molecular mechanisms controlling Schwann cell differentiation and myelination. This knowledge is of key importance for the success of regenerative medicine in peripheral neuropathies, nerve tumors, and transplantation paradigms in non-regenerative CNS lesions and in large PNS injuries. 3 double knockout mutants for HDAC1 and HDAC2 and 3 control littermates were analyzed. Tissues analyzed: sciatic nerves of 2 day-old mouse pups

2011-02-25 | E-GEOD-27451 | biostudies-arrayexpress

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