Three Dimensional Conjugation of Recombinant N-Cadherin to a Hydrogel for In Vitro Anisotropic Neural Growth.

Living cells are extensively being studied to build functional tissues that are useful for both fundamental and applied bioscience studies. Increasing evidence suggests that cell-cell adhesion controlled by intercellular cadherin junction plays important roles in the quality of the resulting engineered tissue. These findings prompted efforts to interrogate biological effects of cadherin at a molecular scale; however, few efforts were made to harness the effects of cadherin on cells cultured in an in vivo-like three dimensional matrix. To this end, this study reports a hydrogel matrix three dimensionally functionalized with a controlled number of Fc-tagged recombinant N-cadherins (N-Cad-Fc). To retain the desired conformation of N-Cad, these cadherins were immobilized and oriented to the gel by anti-Fc-antibodies chemically coupled to gels. The gels were processed to present N-Cad-Fc in uniaxially aligned microchannels or randomly oriented micropores. Culturing cortical cells in the functionalized gels generated a large fraction of neurons that are functional as indicated by increased intracellular calcium ion concentrations with the microchanneled gel. In contrast, direct N-Cad-Fc immobilization to microchannel or micropore walls of the gel limited the growth of neurons and increased the glial to neuron ratio. The results of this study will be highly useful to organize a wide array of cadherin molecules in a series of biomaterials used for three-dimensional cell culture and to regulate phenotypic activities of tissue-forming cells in an elaborate manner.

[1]  S. Willerth,et al.  Approaches to neural tissue engineering using scaffolds for drug delivery. , 2007, Advanced drug delivery reviews.

[2]  Marja-Leena Linne,et al.  Astrocyte-neuron interactions: from experimental research-based models to translational medicine. , 2014, Progress in molecular biology and translational science.

[3]  Bruce C Wheeler,et al.  Neuronal network structuring induces greater neuronal activity through enhanced astroglial development , 2006, Journal of neural engineering.

[4]  S. Skaper Neuronal growth-promoting and inhibitory cues in neuroprotection and neuroregeneration. , 2012, Methods in molecular biology.

[5]  Hynek Wichterle,et al.  Combined microfluidics/protein patterning platform for pharmacological interrogation of axon pathfinding. , 2010, Lab on a chip.

[6]  R. Bashir,et al.  Glacier Moraine Formation‐Mimicking Colloidal Particle Assembly in Microchanneled, Bioactive Hydrogel for Guided Vascular Network Construction , 2015, Advanced healthcare materials.

[7]  E. Newman New roles for astrocytes: Regulation of synaptic transmission , 2003, Trends in Neurosciences.

[8]  Bruce C. Wheeler,et al.  Designing Neural Networks in Culture , 2010, Proceedings of the IEEE.

[9]  Y. Fujii,et al.  Flash freezing route to mesoporous polymer nanofibre networks , 2013, Nature Communications.

[10]  R. Mège,et al.  Immobilized dimers of N-cadherin-Fc chimera mimic cadherin-mediated cell contact formation: contribution of both outside-in and inside-out signals. , 2000, Journal of cell science.

[11]  Emma East,et al.  Engineering an integrated cellular interface in three-dimensional hydrogel cultures permits monitoring of reciprocal astrocyte and neuronal responses. , 2012, Tissue engineering. Part C, Methods.

[12]  R. D. Mastro,et al.  Intracellular Calcium Assays in Dissociated Primary Cortical Neurons , 2009 .

[13]  C. Kay,et al.  Multiple cadherin extracellular repeats mediate homophilic binding and adhesion , 2001, The Journal of cell biology.

[14]  T. Kennedy,et al.  Engineered cell culture substrates for axon guidance studies: moving beyond proof of concept. , 2013, Lab on a chip.

[15]  D. Leckband,et al.  Recapitulating cell-cell adhesion using N-cadherin biologically tethered to substrates. , 2014, Biomacromolecules.

[16]  W Shain,et al.  Fabrication and optimization of alginate hydrogel constructs for use in 3D neural cell culture , 2011, Biomedical materials.

[17]  Peter D. Kwong,et al.  Structural basis of cell-cell adhesion by cadherins , 1995, Nature.

[18]  Mark F Bear,et al.  NMDA Induces Long-Term Synaptic Depression and Dephosphorylation of the GluR1 Subunit of AMPA Receptors in Hippocampus , 1998, Neuron.

[19]  Robert H. Lee,et al.  Three-dimensional neural constructs: a novel platform for neurophysiological investigation , 2008, Journal of neural engineering.

[20]  J. Bixby,et al.  N-cadherin and integrins: Two receptor systems that mediate neuronal process outgrowth on astrocyte surfaces , 1988, Neuron.

[21]  Christine E Schmidt,et al.  Neural tissue engineering: strategies for repair and regeneration. , 2003, Annual review of biomedical engineering.

[22]  G. Radice N-cadherin-mediated adhesion and signaling from development to disease: lessons from mice. , 2013, Progress in molecular biology and translational science.

[23]  D. Leckband,et al.  Direct molecular force measurements of multiple adhesive interactions between cadherin ectodomains. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[24]  M. Takeichi,et al.  Cadherins in neuronal morphogenesis and function , 2008, Development, growth & differentiation.

[25]  Ali Khademhosseini,et al.  Controlling the porosity and microarchitecture of hydrogels for tissue engineering. , 2010, Tissue engineering. Part B, Reviews.

[26]  Yadong Wang,et al.  Materials for central nervous system regeneration: bioactive cues , 2011 .

[27]  D. Mooney,et al.  Alginate: properties and biomedical applications. , 2012, Progress in polymer science.

[28]  Zhifeng Shao,et al.  Fc-fusion proteins: new developments and future perspectives , 2012, EMBO molecular medicine.

[29]  Christian Obinger,et al.  Engineered IgG1‐Fc – one fragment to bind them all , 2016, Immunological reviews.