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Heterogeneous Cardiac- and Neural Crest-Derived Aortic Smooth Muscle Cells have Similar Transcriptional Changes after TGFβ Signaling Disruption [scRNA-seq-of-Wnt1-Cre2-mTmG]

ABSTRACT: Heterogeneous Cardiac- and Neural Crest-Derived Aortic Smooth Muscle Cells have Similar Transcriptional Changes after TGFβ Signaling Disruption [scRNA-seq-of-Wnt1-Cre2-mTmG]

PROVIDER: PRJNA1067701 | ENA |

REPOSITORIES: ENA

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Heterogeneous Cardiac- and Neural Crest-Derived Aortic Smooth Muscle Cells have Similar Transcriptional Changes after TGFβ Signaling Disruption [scRNA-seq-of-Wnt1-Cre2-mTmG]

Project description:We report single-cell RNA-seq data of Wnt1-Cre2 lineage marked, integrin alpha 8 labeled smooth muscle cells (SMCs) from murine aortas at 12 weeks of age

2025-02-27 | GSE253930 | GEO

TGFβ signaling controls neural crest developmental plasticity via Smad2/3

Project description:The neural crest is a highly plastic stem cell population that represents a notable exception to the germ layer theory. Despite being of ectodermal origin, these cells can differentiate into skeletal derivatives like cartilage and bone, tissues that are typically formed by mesoderm. The inductive program that endows the neural crest with these unique properties is still poorly understood. Here, we report that Smad2/3-mediated TGFβ signaling endows cranial neural crest cells with enhanced developmental potential. Our results show that TGFβ signaling modulates neural crest axial identity and directly activates the gene circuits that support skeletal differentiation. Cooperation between TGFβ and low levels of WNT-signaling in the embryonic head activates cranial-specific cis-regulatory elements of anterior genes. Activation of the TGFβ pathway allowed reprogramming of trunk neural crest cells to adopt an anterior identity and led to the development of an improved protocol for the generation of human cranial neural crest cells. Our findings indicate TGFβ signaling is required for the specification of cranial neural crest cells, endowing them with the potential to give rise to the craniofacial skeleton.

2025-01-19 | GSE175808 | GEO

TGFβ signaling controls neural crest developmental plasticity via Smad2/3

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Heterogeneous Cardiac- and Neural Crest-Derived Aortic Smooth Muscle Cells have Similar Transcriptional Changes after TGFβ Signaling Disruption [scRNA-seq-of-human-aortic-cells]

Project description:Heterogeneous Cardiac- and Neural Crest-Derived Aortic Smooth Muscle Cells have Similar Transcriptional Changes after TGFβ Signaling Disruption [scRNA-seq-of-human-aortic-cells]

| PRJNA1067703 | ENA

TGFβ signaling controls neural crest developmental plasticity via Smad2/3 [ATAC-seq]

2025-01-19 | GSE278072 | GEO

TGFβ signaling controls neural crest developmental plasticity via Smad2/3 [RNA-seq]

2025-01-19 | GSE278071 | GEO

TGFβ signaling controls neural crest developmental plasticity via Smad2/3

Project description:TGFβ signaling controls neural crest developmental plasticity via Smad2/3

| PRJNA733778 | ENA

TGFβ signaling controls neural crest developmental plasticity via Smad2/3

Project description:TGFβ signaling controls neural crest developmental plasticity via Smad2/3

| PRJNA733779 | ENA

TGFβ signaling controls neural crest developmental plasticity via Smad2/3

Project description:TGFβ signaling controls neural crest developmental plasticity via Smad2/3

| PRJNA733780 | ENA

miR-302 is a temporal regulator of neural crest development [Mouse miRNA-seq]

Project description:We analyzed wildtype and miR-302 knockout embryos at E7.5 and sorted neural crest using Wnt1-Cre at E8.5 and Sox9 at E9.5 to capture miRNA differences during neural crest development

2020-03-09 | GSE137240 | GEO

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