Noninvasive quantification of in vitro osteoblastic differentiation in 3D engineered tissue constructs using spectral ultrasound imaging

• Published in: PloS one 2014-01, Vol.9 (1), p.e85749-e85749
• Main Authors: Gudur, Madhu Sudhan Reddy, Rao, Rameshwar R, Peterson, Alexis W, Caldwell, David J, Stegemann, Jan P, Deng, Cheri X
• Format: Article
• Language: English
• Subjects: 3T3 Cells; Acoustic attenuation; Acoustic impedance; Acoustics; Animals; Apoptosis; Biocompatibility; Biology; Biomedical engineering; Biomedical materials; Bones; Calcium; Calcium - metabolism; Calcium content; Cell Culture Techniques - instrumentation; Cell Culture Techniques - methods; Cell Differentiation; Cell Size; Cell Survival; Collagen; Collagen - metabolism; Construction engineering; Cytology; Deoxyribonucleic acid; Deposition; Differentiation; DNA; Engineering; Extracellular matrix; Hydrogels; Image resolution; Materials Science; Measurement techniques; Medical imaging; Medicine; Mice; Monitoring; NMR; Nuclear magnetic resonance; Osteoblastogenesis; Osteoblasts; Osteoblasts - cytology; Osteoblasts - diagnostic imaging; Osteoblasts - metabolism; Osteogenesis; Physical properties; Prostate; Quantitation; Reproducibility of Results; Stem cells; Time Factors; Tissue engineering; Tissue Engineering - instrumentation; Tissue Engineering - methods; Ultrasonic imaging; Ultrasonography; Ultrasound; Ultrasound imaging
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0085749

Non-destructive monitoring of engineered tissues is needed for translation of these products from the lab to the clinic. In this study, non-invasive, high resolution spectral ultrasound imaging (SUSI) was used to monitor the differentiation of MC3T3 pre-osteoblasts seeded within collagen hydrogels. SUSI was used to measure the diameter, concentration and acoustic attenuation of scatterers within such constructs cultured in either control or osteogenic medium over 21 days. Conventional biochemical assays were used on parallel samples to determine DNA content and calcium deposition. Construct volume and morphology were accurately imaged using ultrasound. Cell diameter was estimated to be approximately 12.5-15.5 µm using SUSI, which corresponded well to measurements of fluorescently stained cells. The total number of cells per construct assessed by quantitation of DNA content decreased from 5.6±2.4×10(4) at day 1 to 0.9±0.2×10(4) at day 21. SUSI estimation of the equivalent number of acoustic scatters showed a similar decreasing trend, except at day 21 in the osteogenic samples, which showed a marked increase in both scatterer number and acoustic impedance, suggestive of mineral deposition by the differentiating MC3T3 cells. Estimation of calcium content by SUSI was 41.7±11.4 µg/ml, which agreed well with the biochemical measurement of 38.7±16.7 µg/ml. Color coded maps of parameter values were overlaid on B-mode images to show spatiotemporal changes in cell diameter and calcium deposition. This study demonstrates the use of non-destructive ultrasound imaging to provide quantitative information on the number and differentiated state of cells embedded within 3D engineered constructs, and therefore presents a valuable tool for longitudinal monitoring of engineered tissue development.