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Wieland, B. A.

Publications and source records attributed to Wieland, B. A..

2 recordsLinked to original sources

Enteric glial cells of the two plexi of the enteric nervous system exhibit phenotypic and functional inter-and intra-heterogeneity

Enteric glial cells (EGC) are a prominent cell type of all layers of the gut wall, virtually controlling all gastrointestinal functions. While the development of transgenic mice has led to major advances in understanding EGC biology, in vitro models are still fairly limited and do not allow for the robust and reproducible establishment of primary cultures discriminating EGC from the inner versus outer layers of the gut wall. Here we report a novel method to separately grow EGC from the inner and outer layers of the intestinal wall from the same mouse with a high degree of purity and cell heterogeneity. Our results indicate that EGC from the inner layers of the gut wall exhibit higher calcium response to ATP when compared to EGC from the outer layers. We also show that inner EGC cultures express lower levels of the transcription factor Sox 10 as compared to outer EGC cultures, which mirrors in situ differential expression of Sox10 in submucosal (inner) versus myenteric (outer) plexus assessed using wholemounts. Confocal microscopy analyses of wholemounts further demonstrate that a majority of calretinin-expressing ganglionic cells of the submucosal plexus express the EGC marker S-100{beta}, while this population is marginally represented in ganglia of the myenteric plexus. Altogether this study describes a novel method of EGC primary cultures permitting for the first time to compare inner versus outer EGC and provides in vitro and ex vivo evidence that inner EGC and outer EGC are phenotypically and functionally distinct.

neuroscience↗

GFAP-directed Inactivation of Men1 Exploits Glial Cell Plasticity in Favor of Neuroendocrine Reprogramming

BACKGROUND & AIMSEfforts to characterize the signaling mechanisms that underlie gastroenteropancreatic neoplasms (GEP-NENs) are precluded by a lack of comprehensive model systems that recapitulate pathogenesis. Investigation into a potential cell-of-origin for gastrin-secreting NENs revealed a role for enteric glia in neuroendocrine cell specification. Here we investigated the hypothesis that loss of menin in glial cells stimulated neuroendocrine differentiation and tumorigenesis. METHODSUsing Cre-lox technology, we generated a conditional glial fibrillary acidic protein-directed Men1 knockout (GFAP{Delta}Men1) mouse model. Cre specificity was confirmed using a tdTomato reporter. GFAP{Delta}Men1 mice were evaluated for GEP-NEN development and neuroendocrine cell hyperplasia. siRNA-mediated Men1 silencing in a rat enteric glial cell line was performed in parallel. RESULTSGFAP{Delta}Men1 mice developed pancreatic NENs, in addition to pituitary prolactinomas that phenocopied the human MEN1 syndrome. GFAP{Delta}Men1 mice exhibited gastric neuroendocrine hyperplasia that coincided with a significant loss of GFAP expression. Mechanistically, Men1 deletion induced reprogramming from a mature glial phenotype toward a neuroendocrine lineage. Furthermore, blockade of Hedgehog signaling in enteric glia attenuated neuroendocrine hyperplasia by restricting the neuroendocrine cell fate. CONCLUSIONSGFAP-directed Men1 inactivation exploits glial cell plasticity in favor of neuroendocrine differentiation. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=65 SRC="FIGDIR/small/479845v1_ufig1.gif" ALT="Figure 1"> View larger version (21K): org.highwire.dtl.DTLVardef@1118702org.highwire.dtl.DTLVardef@1b6cc3forg.highwire.dtl.DTLVardef@1b4949org.highwire.dtl.DTLVardef@168704b_HPS_FORMAT_FIGEXP M_FIG C_FIG

cancer biology↗