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Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans
Thuy-Linh Le, … , Jeanne Amiel, Nadège Bondurand
Thuy-Linh Le, … , Jeanne Amiel, Nadège Bondurand
Published January 26, 2021
Citation Information: J Clin Invest. 2021;131(6):e145837. https://doi.org/10.1172/JCI145837.
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Research Article Development Gastroenterology

Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans

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Abstract

Hirschsprung disease (HSCR) is the most frequent developmental anomaly of the enteric nervous system, with an incidence of 1 in 5000 live births. Chronic intestinal pseudo-obstruction (CIPO) is less frequent and classified as neurogenic or myogenic. Isolated HSCR has an oligogenic inheritance with RET as the major disease-causing gene, while CIPO is genetically heterogeneous, caused by mutations in smooth muscle–specific genes. Here, we describe a series of patients with developmental disorders including gastrointestinal dysmotility, and investigate the underlying molecular bases. Trio-exome sequencing led to the identification of biallelic variants in ERBB3 and ERBB2 in 8 individuals variably associating HSCR, CIPO, peripheral neuropathy, and arthrogryposis. Thorough gut histology revealed aganglionosis, hypoganglionosis, and intestinal smooth muscle abnormalities. The cell type–specific ErbB3 and ErbB2 function was further analyzed in mouse single-cell RNA sequencing data and in a conditional ErbB3-deficient mouse model, revealing a primary role for ERBB3 in enteric progenitors. The consequences of the identified variants were evaluated using quantitative real-time PCR (RT-qPCR) on patient-derived fibroblasts or immunoblot assays on Neuro-2a cells overexpressing WT or mutant proteins, revealing either decreased expression or altered phosphorylation of the mutant receptors. Our results demonstrate that dysregulation of ERBB3 or ERBB2 leads to a broad spectrum of developmental anomalies, including intestinal dysmotility.

Authors

Thuy-Linh Le, Louise Galmiche, Jonathan Levy, Pim Suwannarat, Debby M.E.I. Hellebrekers, Khomgrit Morarach, Franck Boismoreau, Tom E.J. Theunissen, Mathilde Lefebvre, Anna Pelet, Jelena Martinovic, Antoinette Gelot, Fabien Guimiot, Amanda Calleroz, Cyril Gitiaux, Marie Hully, Olivier Goulet, Christophe Chardot, Severine Drunat, Yline Capri, Christine Bole-Feysot, Patrick Nitschké, Sandra Whalen, Linda Mouthon, Holly E. Babcock, Robert Hofstra, Irenaeus F.M. de Coo, Anne-Claude Tabet, Thierry J. Molina, Boris Keren, Alice Brooks, Hubert J.M. Smeets, Ulrika Marklund, Christopher T. Gordon, Stanislas Lyonnet, Jeanne Amiel, Nadège Bondurand

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Figure 4

Histology of skeletal muscles, the anterior horn of the spinal cord and dorsal root ganglia of fetuses with ERBB3 mutations.

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Histology of skeletal muscles, the anterior horn of the spinal cord and ...
(A–C) H&E-stained sections of muscle specimens from F3:II-1 (A, quadriceps femoris muscle at 16 WG), F3:II-3 (B, deltoid muscle at 15 WG), and F4:II-1 (C, psoas muscle at 18 WG). Note the presence of the unequal caliber of muscle fibers with the presence of numerous myotubes characterized by central nuclei (blue arrows) compared with the control muscles (C-16WG, C-15WG, and C-18WG psoas muscles), where muscle fibers are homogeneous in size and density with most nuclei positioned at the periphery of mature fibers. (D) Analysis at the ultrastructural level by electron microscopy shows isolated primary myotubes (M1) in fetus F4:II-1, while in the control, secondary myotubes (M2) were observed apposed to the primary myotube (M1). (E) Immunohistochemical analyses using NCL-MHCs and NCL-MHCf antibodies (staining slow and fast myosin heavy chains, respectively) showed the presence of type I and II myotubes, respectively. (F) Preserved cyto-architecture of cervical spinal cord of fetus F4:II-1. AH: anterior horn; DRG: dorsal root ganglion. (G) Higher magnification of boxed regions in F. At the cellular level, both motoneurons in the anterior horn (blue arrows in AH) and sensory neurons in the dorsal root ganglia (blue arrows in DRG) displayed normal morphology and density. Scale bars: 100 μm in A–C, E–G; 2 μm in D.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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