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  1. Article ; Online: Loss of ZNF148 enhances insulin secretion in human pancreatic β cells

    Eleonora de Klerk / Yini Xiao / Christopher H. Emfinger / Mark P. Keller / David I. Berrios / Valentina Loconte / Axel A. Ekman / Kate L. White / Rebecca L. Cardone / Richard G. Kibbey / Alan D. Attie / Matthias Hebrok

    JCI Insight, Vol 8, Iss

    2023  Volume 11

    Abstract: Insulin secretion from pancreatic β cells is essential to the maintenance of glucose homeostasis. Defects in this process result in diabetes. Identifying genetic regulators that impair insulin secretion is crucial for the identification of novel ... ...

    Abstract Insulin secretion from pancreatic β cells is essential to the maintenance of glucose homeostasis. Defects in this process result in diabetes. Identifying genetic regulators that impair insulin secretion is crucial for the identification of novel therapeutic targets. Here, we show that reduction of ZNF148 in human islets, and its deletion in stem cell–derived β cells (SC–β cells), enhances insulin secretion. Transcriptomics of ZNF148-deficient SC–β cells identifies increased expression of annexin and S100 genes whose proteins form tetrameric complexes involved in regulation of insulin vesicle trafficking and exocytosis. ZNF148 in SC–β cells prevents translocation of annexin A2 from the nucleus to its functional place at the cell membrane via direct repression of S100A16 expression. These findings point to ZNF148 as a regulator of annexin-S100 complexes in human β cells and suggest that suppression of ZNF148 may provide a novel therapeutic strategy to enhance insulin secretion.
    Keywords Metabolism ; Stem cells ; Medicine ; R
    Subject code 571
    Language English
    Publishing date 2023-06-01T00:00:00Z
    Publisher American Society for Clinical investigation
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Single-cell transcriptional profiling of human thymic stroma uncovers novel cellular heterogeneity in the thymic medulla

    Jhoanne L. Bautista / Nathan T. Cramer / Corey N. Miller / Jessica Chavez / David I. Berrios / Lauren E. Byrnes / Joe Germino / Vasilis Ntranos / Julie B. Sneddon / Trevor D. Burt / James M. Gardner / Chun J. Ye / Mark S. Anderson / Audrey V. Parent

    Nature Communications, Vol 12, Iss 1, Pp 1-

    2021  Volume 15

    Abstract: The thymus supports T cell immunity by providing the environment for thymocyte differentiation. Here the authors profile human thymic stroma at the single cell level, identifying ionocytes as a new medullary population and defining tissue specific ... ...

    Abstract The thymus supports T cell immunity by providing the environment for thymocyte differentiation. Here the authors profile human thymic stroma at the single cell level, identifying ionocytes as a new medullary population and defining tissue specific antigen expression in multiple stromal cell types.
    Keywords Science ; Q
    Language English
    Publishing date 2021-02-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Single-cell transcriptome analysis defines heterogeneity of the murine pancreatic ductal tree

    Audrey M Hendley / Arjun A Rao / Laura Leonhardt / Sudipta Ashe / Jennifer A Smith / Simone Giacometti / Xianlu L Peng / Honglin Jiang / David I Berrios / Mathias Pawlak / Lucia Y Li / Jonghyun Lee / Eric A Collisson / Mark S Anderson / Gabriela K Fragiadakis / Jen Jen Yeh / Chun Jimmie Ye / Grace E Kim / Valerie M Weaver /
    Matthias Hebrok

    eLife, Vol

    2021  Volume 10

    Abstract: To study disease development, an inventory of an organ's cell types and understanding of physiologic function is paramount. Here, we performed single-cell RNA-sequencing to examine heterogeneity of murine pancreatic duct cells, pancreatobiliary cells, ... ...

    Abstract To study disease development, an inventory of an organ's cell types and understanding of physiologic function is paramount. Here, we performed single-cell RNA-sequencing to examine heterogeneity of murine pancreatic duct cells, pancreatobiliary cells, and intrapancreatic bile duct cells. We describe an epithelial-mesenchymal transitory axis in our three pancreatic duct subpopulations and identify osteopontin as a regulator of this fate decision as well as human duct cell dedifferentiation. Our results further identify functional heterogeneity within pancreatic duct subpopulations by elucidating a role for geminin in accumulation of DNA damage in the setting of chronic pancreatitis. Our findings implicate diverse functional roles for subpopulations of pancreatic duct cells in maintenance of duct cell identity and disease progression and establish a comprehensive road map of murine pancreatic duct cell, pancreatobiliary cell, and intrapancreatic bile duct cell homeostasis.
    Keywords scRNA-seq ; pancreatic duct ligation ; Osteopontin ; Geminin ; duct heterogeneity ; Medicine ; R ; Science ; Q ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2021-05-01T00:00:00Z
    Publisher eLife Sciences Publications Ltd
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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