Literature DB >> 24675920

Sensory neurons and osteoblasts: close partners in a microfluidic platform.

Estrela Neto1, Cecília J Alves, Daniela M Sousa, Inês S Alencastre, Ana H Lourenço, Luís Leitão, Hyun R Ryu, Noo L Jeon, Rui Fernandes, Paulo Aguiar, Ramiro D Almeida, Meriem Lamghari.   

Abstract

Innervation has proven to be critical in bone homeostasis/regeneration due to the effect of soluble factors, produced by nerve fibers, associated with changes in the activity of bone cells. Thus, in this study, we have established and characterized a coculture system comprising sensory neurons and osteoblasts to mimic the in vivo scenario where nerve fibers can be found in a bone microenvironment. Embryonic or adult primary dorsal root ganglion (DRG) and MC3T3-E1 osteoblastic cells were cocultured in compartmentalized microfluidic platforms and morphological and functional tests were performed. The time of adhesion and readout of axonal outgrowth were improved by the alignment of DRG with the axis of microgrooves, which showed to be a crucial step for the designed experiments. Cocultures of entire DRG from adult origin with osteoblasts were performed, showing extended DRG projections towards the axonal compartment, reaching osteoblastic cells. Immunocytochemistry showed that the neurites present within the osteoblastic compartment were immunoreactive to synapsin and calcitonin gene-related peptide suggesting the presence of specialized structures involved in this crosstalk. This evidence was further confirmed by electron microscopy where varicosities were detected as well as electron dense structures in neurite membranes. Aiming to mimic the properties of tissue extracellular matrices, MC3T3-E1 cells were seeded in the axonal side upon laminin, collagen or within 3D functionalized alginate matrices and axonal outgrowth was clearly observed. In order to analyze and quantify data with reproducible image analysis, a semi-automated algorithm was also developed. The collagen and laminin substrates displayed a higher amount of axons reaching the axonal side. Overall, the established method revealed to be a suitable tool to study the interaction between the peripheral nervous system and bone cells in different contexts mimicking the in vivo scenario.

Entities:  

Mesh:

Year:  2014        PMID: 24675920     DOI: 10.1039/c4ib00035h

Source DB:  PubMed          Journal:  Integr Biol (Camb)        ISSN: 1757-9694            Impact factor:   2.192


  18 in total

1.  Analysis of Developing Tooth Germ Innervation Using Microfluidic Co-culture Devices.

Authors:  Pierfrancesco Pagella; Shayee Miran; Tim Mitsiadis
Journal:  J Vis Exp       Date:  2015-08-14       Impact factor: 1.355

Review 2.  Advances in ex vivo models and lab-on-a-chip devices for neural tissue engineering.

Authors:  Sahba Mobini; Young Hye Song; Michaela W McCrary; Christine E Schmidt
Journal:  Biomaterials       Date:  2018-05-11       Impact factor: 12.479

3.  Osteoblasts are inherently programmed to repel sensory innervation.

Authors:  Luís Leitão; Estrela Neto; Francisco Conceição; Ana Monteiro; Marina Couto; Cecília J Alves; Daniela M Sousa; Meriem Lamghari
Journal:  Bone Res       Date:  2020-05-13       Impact factor: 13.567

4.  Microfluidic neurite guidance to study structure-function relationships in topologically-complex population-based neural networks.

Authors:  Thibault Honegger; Moritz I Thielen; Soheil Feizi; Neville E Sanjana; Joel Voldman
Journal:  Sci Rep       Date:  2016-06-22       Impact factor: 4.379

5.  Axonal outgrowth, neuropeptides expression and receptors tyrosine kinase phosphorylation in 3D organotypic cultures of adult dorsal root ganglia.

Authors:  Estrela Neto; Cecília J Alves; Luís Leitão; Daniela M Sousa; Inês S Alencastre; Francisco Conceição; Meriem Lamghari
Journal:  PLoS One       Date:  2017-07-24       Impact factor: 3.240

6.  Mesenchymal stem cells secretome-induced axonal outgrowth is mediated by BDNF.

Authors:  Luís F Martins; Rui O Costa; Joana R Pedro; Paulo Aguiar; Sofia C Serra; Fabio G Teixeira; Nuno Sousa; António J Salgado; Ramiro D Almeida
Journal:  Sci Rep       Date:  2017-06-23       Impact factor: 4.379

7.  Activation of microglia bolsters synapse formation.

Authors:  Gonçalo Cristovão; Maria J Pinto; Rodrigo A Cunha; Ramiro D Almeida; Catarina A Gomes
Journal:  Front Cell Neurosci       Date:  2014-06-02       Impact factor: 5.505

8.  Microfluidics co-culture systems for studying tooth innervation.

Authors:  Pierfrancesco Pagella; Estrela Neto; Lucia Jiménez-Rojo; Meriem Lamghari; Thimios A Mitsiadis
Journal:  Front Physiol       Date:  2014-08-25       Impact factor: 4.566

9.  The proteasome controls presynaptic differentiation through modulation of an on-site pool of polyubiquitinated conjugates.

Authors:  Maria J Pinto; Pedro L Alves; Luís Martins; Joana R Pedro; Hyun R Ryu; Noo Li Jeon; Anne M Taylor; Ramiro D Almeida
Journal:  J Cell Biol       Date:  2016-03-28       Impact factor: 10.539

10.  Visualizing K48 Ubiquitination during Presynaptic Formation By Ubiquitination-Induced Fluorescence Complementation (UiFC).

Authors:  Maria J Pinto; Joana R Pedro; Rui O Costa; Ramiro D Almeida
Journal:  Front Mol Neurosci       Date:  2016-06-10       Impact factor: 5.639

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