A long-term goal of the research in our laboratory is to re-create the components and compartments of mammalian systems, and in particular human systems, to engineer functional hybrid models. The initial period for this Bioengineering Research Grant (BRG) was to investigate the motoneuron to muscle segment of the reflex arc to understand in vitro what are possible outcomes when a human stem cell is implanted in a rat model and then apply it to improve the outcomes in an in vivo system. We have made a number of breakthroughs with this model system that move us closer to the goal of creating a functional in vitro model of the reflex arc: 1) We have cultivated embryonic and adult rat motoneurons as well as motoneurons derived from human fetal stem cells (hFSC). 2) We have demonstrated neuromuscular junction formation between these rat and human derived motoneurons with myotubes derived from both rat and human adult satellite cells. However, we have also created mature myotubes that exhibit sarcomere formation, express myosin heavy chain, have established the EC coupling apparatus as well as Type I and Type II muscle isoforms. We have also differentiated the myotubes into intrafusal fibers and integrated then with the MEMS constructs and demonstrated that these are functional mechanoreceptor synapses. 3) Glial cells have been incorporated into our model system and we have demonstrated Schwann cell myelination of motoneurons, with complete Node of Ranvier formation, and derived pure populations of MBP (myelin basic protein) positive oligodendrocytes from human mesenchymal stem cells. 4) We have successfully demonstrated in vivo integration of the differentiated hFSC derived motoneurons into an adult rat spinal cord injury model and shown significant locomotor recovery as accessed via the BBB test scoring system. This renewal BRG application seeks to complete the development of the entire reflex arc in vitro using primary rat cells and then with cells derived from human stem cells. We will also initiate experiments to increase the throughput of first the motoneurons to muscle segment of the stretch reflex are and then for the entire reflex arc. The Hypothesis is that we can recreate a functional in vitro model of the reflex arc with primary rat cells and achieve the same result with cells derived from human stem cells that will be a prototype for the next generation screens for drug discovery and toxicology. The continuation of the grant will enable advances for 1) the creation of a human cell based reflex arc in a defined, serum-free environment and 2) the development of new technology for utilization in the next level of Systems Biology and high-information content screens. Our expertise in surface chemistry, Micro-ElectroMechanical Systems (MEMS) fabrication and developmental/cellular/molecular biology has now allowed the construction of complex functional neuronal systems in vitro. Our team possesses the necessary expertise in all aspects of this project, as well as the facilities to effectively and successfully perform the research.
The goal of this project is to engineer a system to model one of the most fundamental motor circuits in the human body, the spinal reflex arc. We will use nanotechnology and microelectronics in combination with biomedical engineering techniques to build this hybrid biological/non-biological system. Potential benefits include prevention, diagnosis, and treatment of developmental abnormalities in the spinal cord, rehabilitation of chronic neurological/muscle disorders and accompanying pain, and new strategies for prosthetic and orthotic design and evaluation.
|Berry, Bonnie J; Smith, Alec S T; Long, Christopher J et al. (2018) Physiological A? Concentrations Produce a More Biomimetic Representation of the Alzheimer's Disease Phenotype in iPSC Derived Human Neurons. ACS Chem Neurosci 9:1693-1701|
|Santhanam, Navaneetha; Kumanchik, Lee; Guo, Xiufang et al. (2018) Stem cell derived phenotypic human neuromuscular junction model for dose response evaluation of therapeutics. Biomaterials 166:64-78|
|Wang, Ying I; Carmona, Carlos; Hickman, James J et al. (2018) Multiorgan Microphysiological Systems for Drug Development: Strategies, Advances, and Challenges. Adv Healthc Mater 7:|
|Lavado, Andrea; Guo, Xiufang; Smith, Alec St et al. (2017) Evaluation of Holistic Treatment for ALS Reveals Possible Mechanism and Therapeutic Potential. Int J Pharm Pharm Res 11:348-374|
|Guo, Xiufang; Colon, Alisha; Akanda, Nesar et al. (2017) Tissue engineering the mechanosensory circuit of the stretch reflex arc with human stem cells: Sensory neuron innervation of intrafusal muscle fibers. Biomaterials 122:179-187|
|Colón, A; Guo, X; Akanda, N et al. (2017) Functional analysis of human intrafusal fiber innervation by human ?-motoneurons. Sci Rep 7:17202|
|McAleer, Christopher W; Rumsey, John W; Stancescu, Maria et al. (2015) Functional myotube formation from adult rat satellite cells in a defined serum-free system. Biotechnol Prog 31:997-1003|
|Thakore, Vaibhav; Hickman, James J (2015) Charge Relaxation Dynamics of an Electrolytic Nanocapacitor. J Phys Chem C Nanomater Interfaces 119:2121-2132|
|Wilson, Kerry A; Finch, Craig A; Anderson, Phillip et al. (2015) Combining an optical resonance biosensor with enzyme activity kinetics to understand protein adsorption and denaturation. Biomaterials 38:86-96|
|Sung, Jong Hwan; Srinivasan, Balaji; Esch, Mandy Brigitte et al. (2014) Using physiologically-based pharmacokinetic-guided ""body-on-a-chip"" systems to predict mammalian response to drug and chemical exposure. Exp Biol Med (Maywood) 239:1225-39|
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