Transcription and Signaling Regulators in Developing Neuronal Subtypes of Mouse and Human Enteric Nervous System

被引:61
|
作者
Memic, Fatima [1 ]
Knoflach, Viktoria [1 ]
Morarach, Khomgrit [1 ]
Sadler, Rebecca [1 ]
Laranjeira, Catia [2 ]
Hjerling-Leffler, Jens [1 ]
Sundstrom, Erik [3 ,4 ]
Pachnis, Vassilis [5 ]
Marklund, Ulrika [1 ]
机构
[1] Karolinska Inst, Div Mol Neurobiol, Dept Med Biochem & Biophys, Scheeles Vag 1, SE-17177 Stockholm, Sweden
[2] MRC, Natl Inst Med Res, Div Mol Neurobiol, London, England
[3] Karolinska Inst, Div Neurodegenerat, Dept Neurobiol Care Sci & Soc, Stockholm, Sweden
[4] Stockholms Sjukhem, Stockholm, Sweden
[5] Francis Crick Inst, London, England
基金
英国医学研究理事会; 英国惠康基金; 瑞典研究理事会;
关键词
HOX; Tyrosine Hydroxylase; Gastric Motility; Neural Crest; DOPAMINERGIC-NEURONS; CELL THERAPY; DIFFERENTIATION; NEUROGENESIS; PROMOTES; IDENTITY; LINEAGE; GENES; SOX6;
D O I
10.1053/j.gastro.2017.10.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: The enteric nervous system (ENS) regulates gastrointestinal function via different subtypes of neurons, organized into fine-tuned neural circuits. It is not clear how cell diversity is created within the embryonic ENS; information required for development of cell-based therapies and models of enteric neuropathies. We aimed to identify proteins that regulate ENS differentiation and network formation. METHODS: We generated and compared RNA expression profiles of the entire ENS, ENS progenitor cells, and non-ENS gut cells of mice, collected at embryonic days 11.5 and 15.5, when different subtypes of neurons are formed. Gastrointestinal tissues from R26ReYFP reporter mice crossed to Sox10-CreER(T2) or Wnt1-Cre mice were dissected and the 6 populations of cells were isolated by flow cytometry. We used histochemistry to map differentially expressed proteins in mouse and human gut tissues at different stages of development, in different regions. We examined enteric neuronal diversity and gastric function in Wnt1-Cre x Sox6(fl/fl) mice, which do not express the Sox6 gene in the ENS. RESULTS: We identified 147 transcription and signaling factors that varied in spatial and temporal expression during development of the mouse ENS. Of the factors also analyzed in human ENS, most were conserved. We uncovered 16 signaling pathways (such as fibroblast growth factor and Eph/ephrin pathways). Transcription factors were grouped according to their specific expression in enteric progenitor cells (such as MEF2C), enteric neurons (such as SOX4), or neuron sub-populations (such as SATB1 and SOX6). Lack of SOX6 in the ENS reduced the numbers of gastric dopamine neurons and delayed gastric emptying. CONCLUSIONS: Using transcriptome and histochemical analyses of the developing mouse and human ENS, we mapped expression patterns of transcription and signaling factors. Further studies of these candidate determinants might elucidate the mechanisms by which enteric stem cells differentiate into neuronal subtypes and form distinct connectivity patterns during ENS development. We found expression of SOX6 to be required for development of gastric dopamine neurons.
引用
收藏
页码:624 / 636
页数:13
相关论文
共 50 条
  • [41] Expression and function of Neuregulin 1 and its signaling system ERBB2/3 in the enteric nervous system
    Barrenschee, Martina
    Lange, Christina
    Cossais, Francois
    Egberts, Jan-Hendrik
    Becker, Thomas
    Wedel, Thilo
    Boettner, Martina
    FRONTIERS IN CELLULAR NEUROSCIENCE, 2015, 9
  • [42] Thrombopoietin gene expression in the developing human central nervous system
    Dame, C
    Wolber, EM
    Freitag, P
    Hofmann, D
    Bartmann, P
    Fandrey, J
    DEVELOPMENTAL BRAIN RESEARCH, 2003, 143 (02): : 217 - 223
  • [43] Expression of the Wnt Receptor Frizzled-4 in the Human Enteric Nervous System of Infants
    Nothelfer, Katharina
    Obermayr, Florian
    Belz, Nadine
    Reinartz, Ellen
    Bareiss, Petra M.
    Buehring, Hans-Joerg
    Beschorner, Rudi
    Just, Lothar
    STEM CELLS INTERNATIONAL, 2016, 2016
  • [44] The distribution of the proteoglycan FORSE-1 in the developing mouse central nervous system
    Kelly, Albert
    O'Malley, Aisling
    Redha, Mohammad
    O'Keeffe, Gerard W.
    Barry, Denis S.
    JOURNAL OF ANATOMY, 2019, 234 (02) : 216 - 226
  • [45] Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new players
    Bondurand, Nadege
    Southard-Smith, E. Michelle
    DEVELOPMENTAL BIOLOGY, 2016, 417 (02) : 139 - 157
  • [46] Ibuprofen slows migration and inhibits bowel colonization by enteric nervous system precursors in zebrafish, chick and mouse
    Schill, Ellen Merrick
    Lake, Jonathan I.
    Tusheva, Olga A.
    Nagy, Nandor
    Bery, Saya K.
    Foster, Lynne
    Avetisyan, Marina
    Johnson, Stephen L.
    Stenson, William F.
    Goldstein, Allan M.
    Heuckeroth, Robert O.
    DEVELOPMENTAL BIOLOGY, 2016, 409 (02) : 473 - 488
  • [47] Human enteric nervous system progenitor transplantation improves functional responses in Hirschsprung disease patient-derived tissue
    Jevans, Benjamin
    Cooper, Fay
    Fatieieva, Yuliia
    Gogolou, Antigoni
    Kang, Yi-Ning
    Restuadi, Restuadi
    Moulding, Dale
    Vanden Berghe, Pieter
    Adameyko, Igor
    Thapar, Nikhil
    Andrews, Peter W.
    De Coppi, Paolo
    Tsakiridis, Anestis
    McCann, Conor J.
    GUT, 2024, 73 (09) : 1441 - 1453
  • [48] SoxD transcription factor deficiency in Schwann cells delays myelination in the developing peripheral nervous system
    Ittner, Ella
    Hartwig, Anna C.
    Elsesser, Olga
    Wuest, Hannah M.
    Froeb, Franziska
    Wedel, Miriam
    Schimmel, Margit
    Tamm, Ernst R.
    Wegner, Michael
    Sock, Elisabeth
    SCIENTIFIC REPORTS, 2021, 11 (01)
  • [49] Expression pattern of BM88 in the developing nervous system of the chick and mouse embryo
    Politis, Panaglotis K.
    Rohrer, Hermann
    Matsas, Rebecca
    GENE EXPRESSION PATTERNS, 2007, 7 (1-2) : 165 - 177
  • [50] Expression of proliferating cell nuclear antigen (PCNA) in the adult and developing mouse nervous system
    Ino, H
    Chiba, T
    MOLECULAR BRAIN RESEARCH, 2000, 78 (1-2): : 163 - 174