Literature DB >> 31200143

Neurturin-containing laminin matrices support innervated branching epithelium from adult epithelial salispheres.

K H Vining1, I M A Lombaert2, V N Patel3, S E Kibbey3, S Pradhan-Bhatt4, R L Witt5, M P Hoffman6.   

Abstract

Cell transplantation of autologous adult biopsies, grown ex vivo as epithelial organoids or expanded as spheroids, are proposed treatments to regenerate damaged branching organs. However, it is not clear whether transplantation of adult organoids or spheroids alone is sufficient to initiate a fetal-like program of branching morphogenesis in which coordinated branching of multiple cell types including nerves, mesenchyme and blood vessels occurs. Yet this is an essential concept for the regeneration of branching organs such as lung, pancreas, and lacrimal and salivary glands. Here, we used factors identified from fetal organogenesis to maintain and expand adult murine and human epithelial salivary gland progenitors in non-adherent spheroid cultures, called salispheres. These factors stimulated critical developmental pathways, and increased expression of epithelial progenitor markers such as Keratin5, Keratin14, FGFR2b and KIT. Moreover, physical recombination of adult salispheres in a laminin-111 extracellular matrix with fetal salivary mesenchyme, containing endothelial and neuronal cells, only induced branching morphogenesis when neurturin, a neurotrophic factor, was added to the matrix. Neurturin was essential to improve neuronal survival, axon outgrowth, innervation of the salispheres, and resulted in the formation of branching structures with a proximal-distal axis that mimicked fetal branching morphogenesis, thus recapitulating organogenesis. Epithelial progenitors were also maintained, and developmental differentiation programs were initiated, showing that the fetal microenvironment provides a template for adult epithelial progenitors to initiate branching and differentiation. Further delineation of secreted and physical cues from the fetal niche will be useful to develop novel regenerative therapies that instruct adult salispheres to resume a developmental-like program in vitro and to regenerate branching organs in vivo. Published by Elsevier Ltd.

Entities:  

Keywords:  Adult epithelial progenitors; Bioengineering; Branching morphogenesis; Ex vivo expansion; Fetal microenvironment; Regenerative medicine; Salivary gland

Mesh:

Substances:

Year:  2019        PMID: 31200143      PMCID: PMC6720117          DOI: 10.1016/j.biomaterials.2019.119245

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  54 in total

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Authors:  Eckhard Lammert; Ondine Cleaver; Douglas Melton
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Journal:  Science       Date:  1953-07-10       Impact factor: 47.728

3.  Identification and characterization of a novel prespheroid 3-dimensional hepatocyte monolayer on galactosylated substratum.

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4.  FGFR2b signaling regulates ex vivo submandibular gland epithelial cell proliferation and branching morphogenesis.

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Journal:  Development       Date:  2005-02-16       Impact factor: 6.868

5.  Keratin 14 immunoreactive cells in pleomorphic adenomas and adenoid cystic carcinomas of salivary glands.

Authors:  Y Ogawa; S Toyosawa; T Ishida; N Ijuhin
Journal:  Virchows Arch       Date:  2000-07       Impact factor: 4.064

6.  EGF-dependent lobule formation and FGF7-dependent stalk elongation in branching morphogenesis of mouse salivary epithelium in vitro.

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Journal:  Dev Dyn       Date:  1999-06       Impact factor: 3.780

7.  Gene targeting reveals a critical role for neurturin in the development and maintenance of enteric, sensory, and parasympathetic neurons.

Authors:  R O Heuckeroth; H Enomoto; J R Grider; J P Golden; J A Hanke; A Jackman; D C Molliver; M E Bardgett; W D Snider; E M Johnson; J Milbrandt
Journal:  Neuron       Date:  1999-02       Impact factor: 17.173

8.  Retarded growth and deficits in the enteric and parasympathetic nervous system in mice lacking GFR alpha2, a functional neurturin receptor.

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Journal:  Neuron       Date:  1999-02       Impact factor: 17.173

9.  Distribution of p63, cytokeratins 5/6 and cytokeratin 14 in 51 normal and 400 neoplastic human tissue samples using TARP-4 multi-tumor tissue microarray.

Authors:  Jorge S Reis-Filho; Pete T Simpson; Albino Martins; Ana Preto; Fátima Gärtner; Fernando C Schmitt
Journal:  Virchows Arch       Date:  2003-07-16       Impact factor: 4.064

10.  Establishment, characterization, and long-term maintenance of cultures of human fetal hepatocytes.

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Review 4.  Tissue Engineered Neurovascularization Strategies for Craniofacial Tissue Regeneration.

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5.  Development of a functional salivary gland tissue chip with potential for high-content drug screening.

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7.  CERE-120 Prevents Irradiation-Induced Hypofunction and Restores Immune Homeostasis in Porcine Salivary Glands.

Authors:  Isabelle M A Lombaert; Vaishali N Patel; Christina E Jones; Derrick C Villier; Ashley E Canada; Matthew R Moore; Elsa Berenstein; Changyu Zheng; Corinne M Goldsmith; John A Chorini; Daniel Martin; Lee Zourelias; Mark G Trombetta; Paul C Edwards; Kathleen Meyer; Dale Ando; Michael J Passineau; Matthew P Hoffman
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