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IL-13 promotes sensory-sympathetic neurons crosstalk in asthma [RNA-seq II]

ABSTRACT: IL-13 promotes sensory-sympathetic neurons crosstalk in asthma

ORGANISM(S): Mus musculus

PROVIDER: GSE227968 | GEO | 2023/03/23

REPOSITORIES: GEO

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IL-13 promotes sensory-sympathetic neurons crosstalk in asthma

Project description:IL-13 promotes sensory-sympathetic neurons crosstalk in asthma

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IL-13 promotes sensory-sympathetic neurons crosstalk in asthma [RNA-seq II]

Project description:IL-13 promotes sensory-sympathetic neurons crosstalk in asthma [RNA-seq II]

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IL-13 promotes sensory-sympathetic neurons crosstalk in asthma [RNA-seq I]

Project description:IL-13 promotes sensory-sympathetic neurons crosstalk in asthma [RNA-seq I]

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IL-13 promotes sensory-sympathetic neurons crosstalk in asthma

Project description:This SuperSeries is composed of the SubSeries listed below.

2023-03-23 | GSE228028 | GEO

IL-13 promotes sensory-sympathetic neurons crosstalk in asthma [RNA-seq I]

Project description:Sequencing of different cell populations of the Jugular-nodose complex (JNC) in a mouse model of Allergic inflammation, and sequencing of cultured JNC nociceptors exposed to IL-13.

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Diversity of satellite glia in sympathetic and sensory ganglia

Project description:Satellite glia are the major glial type found in ganglia of the peripheral nervous system that wrap around cell bodies of sympathetic and sensory neurons that are very diverse. Other than their close physical association with peripheral neurons, little is known about this glial population. Here, we performed single cell RNA sequencing analysis and identified five different populations of satellite glia from sympathetic and sensory ganglia. We identify three shared populations of satellite glia enriched in immune-response genes, immediate-early genes and ion channels/ECM-interactors, respectively. Sensory- and sympathetic-specific satellite glia are differentially enriched for modulators of lipid metabolism. Sensory glia are also specifically enriched for genes involved in glutamate turnover. Further, satellite glia and Schwann cells can be distinguished by unique transcriptional signatures. This study reveals remarkable heterogeneity of satellite glia in the peripheral nervous system.

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PGA Murine IL-13 Asthma

Project description:The IL-13 is a central mediator of allergic asthma. This project investigates the mechanisms by which IL-13 elicits the symptoms of asthma. Keywords: other

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Motor nerves direct the development of the sympathetic nervous system

Project description:The sympathetic nervous system controls a wide spectrum of bodily functions including operation of vessels, cardiac rhythm, and the “flight or fight response”. Sympathetic neurons, which are neural crest-derived, develop in coordination with presynaptic motor nerves extending from the central nervous system (CNS). By using nerve-selective genetic ablations, we revealed that sympathetic ganglia development depends on CNS-derived motor innervation. In the absence of preganglionic motor nerves, trunk sympathetic chain ganglia were fragmented and smaller in size, while cervical ganglia were severely misshapen. Sympathetic neurons were misplaced along sensory fibers and projected towards abnormal paths, in some cases invading the sensory dorsal root ganglia. The misplaced progenitors of sympathoblasts corresponded to the nerve-associated, neural crest-derived Schwann cell precursors (SCPs). Notably, we found that SCPs activate the autonomic marker PHOX2B while migrating along motor nerves towards the region of the dorsal aorta in wildtype embryos, suggesting that SCP differentiate into sympathetic neurons while still nerve-associated in motor-ablated embryos. Ligand-receptor prediction from single cell transcriptomic data coupled with functional studies identified Semaphorin 3A/3F as candidate motor nerve-derived signals influencing neural crest migration along axons. Thus, motor nerves control the placement of sympathoblasts and their subsequent axonal navigation during critical periods of sympathetic chain development.

2024-07-14 | GSE261748 | GEO

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