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A Lab-On-A-Chip Platform for Stimulating Osteocyte Mechanotransduction and Analyzing Functional Outcomes of Bone Remodeling
Published on: May 21, 2020
Bone on-a-chip: a 3D dendritic network in a screening platform for osteocyte-targeted drugs
Maria Veronica Lipreri1, Gemma Di Pompo2, Elisa Boanini3
1Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Abstract:
Age-related musculoskeletal disorders, including osteoporosis, are frequent and associated with long lasting morbidity, in turn significantly impacting on healthcare system sustainability. There is therefore a compelling need to develop reliable preclinical models of disease and drug screening to validate novel drugs possibly on a personalized basis, without the need ofin vivoassay. In the context of bone tissue, although the osteocyte (Oc) network is a well-recognized therapeutic target, currentin vitropreclinical models are unable to mimic its physiologically relevant and highly complex structure. To this purpose, several features are needed, including an osteomimetic extracellular matrix, dynamic perfusion, and mechanical cues (e.g. shear stress) combined with a three-dimensional (3D) culture of Oc. Here we describe, for the first time, a high throughput microfluidic platform based on 96-miniaturized chips for large-scale preclinical evaluation to predict drug efficacy. We bioengineered a commercial microfluidic device that allows real-time visualization and equipped with multi-chips by the development and injection of a highly stiff bone-like 3D matrix, made of a blend of collagen-enriched natural hydrogels loaded with hydroxyapatite nanocrystals. The microchannel, filled with the ostemimetic matrix and Oc, is subjected to passive perfusion and shear stress. We used scanning electron microscopy for preliminary material characterization. Confocal microscopy and fluorescent microbeads were used after material injection into the microchannels to detect volume changes and the distribution of cell-sized objects within the hydrogel. The formation of a 3D dendritic network of Oc was monitored by measuring cell viability, evaluating phenotyping markers (connexin43, integrin alpha V/CD51, sclerostin), quantification of dendrites, and responsiveness to an anabolic drug. The platform is expected to accelerate the development of new drug aimed at modulating the survival and function of osteocytes.
Insights
This study introduces a novel microfluidic platform for high-throughput drug screening to combat age-related bone disorders. The system effectively models the complex osteocyte network, accelerating the development of new osteoporosis treatments.
Area of Science:
- Biomaterials Engineering
- Musculoskeletal Research
- Drug Discovery
Background:
- Age-related musculoskeletal disorders like osteoporosis pose a significant healthcare burden.
- Current in vitro models fail to replicate the complex osteocyte network, hindering drug development.
- There is a need for advanced preclinical models for personalized drug screening.
Purpose of the Study:
- To develop a high-throughput microfluidic platform for preclinical evaluation of drugs targeting osteocytes.
- To create an osteomimetic 3D matrix within a microfluidic device that incorporates dynamic perfusion and mechanical cues.
- To enable large-scale drug screening for osteoporosis and related bone diseases.
Main Methods:
- Bioengineered a 96-miniaturized chip microfluidic platform with a bone-like 3D matrix (collagen-hydroxyapatite hydrogel).
- Incorporated osteocytes (Oc) within the matrix, subjected to passive perfusion and shear stress.
- Utilized scanning electron microscopy, confocal microscopy, and cell phenotyping markers to analyze the osteocyte network and drug response.
Main Results:
- Successfully created a 3D osteocyte network within an osteomimetic matrix in a microfluidic system.
- Demonstrated real-time monitoring of cell viability, dendrite formation, and phenotyping markers.
- Validated the platform's responsiveness to an anabolic drug, showing potential for predicting drug efficacy.
Conclusions:
- The developed microfluidic platform offers a novel, high-throughput method for preclinical drug evaluation in bone tissue engineering.
- This osteocyte-focused model can significantly accelerate the discovery of drugs targeting musculoskeletal disorders.
- The platform facilitates personalized drug screening, potentially improving treatment strategies for osteoporosis.
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