Three-Dimensional Cell Culture Micro-CT Visualization within Collagen Scaffolds in an Aqueous Environment

• Published in: Cells (Basel, Switzerland) Switzerland), 2024-08, Vol.13 (15), p.1234
• Main Authors: Tkachev, Sergey, Chepelova, Natalia, Galechyan, Gevorg, Ershov, Boris, Golub, Danila, Popova, Elena, Antoshin, Artem, Giliazova, Aliia, Voloshin, Sergei, Efremov, Yuri, Istranova, Elena, Timashev, Peter
• Format: Article
• Language: English
• Subjects: Acids; Animals; Biocompatibility; Biodegradability; bioinspired materials; Cartilage; Cell culture; Cell Culture Techniques, Three Dimensional - methods; Cells; Collagen; Collagen - chemistry; Collagen - metabolism; collagen scaffolds; Computed tomography; confocal microscopy; Contrast agents; Contrast media; CT imaging; Humans; in vitro models; International economic relations; micro-CT; Microscopy; Phosphates; Pores; Porosity; Scientific equipment and supplies industry; spatial biology; Tissue culture; Tissue engineering; Tissue Engineering - methods; Tissue Scaffolds - chemistry; Tungsten compounds; Ultrasonic imaging; Visualization; Visualization (Computers); Water - chemistry; X-Ray Microtomography - methods
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells13151234

Among all of the materials used in tissue engineering in order to develop bioequivalents, collagen shows to be the most promising due to its superb biocompatibility and biodegradability, thus becoming one of the most widely used materials for scaffold production. However, current imaging techniques of the cells within collagen scaffolds have several limitations, which lead to an urgent need for novel methods of visualization. In this work, we have obtained groups of collagen scaffolds and selected the contrasting agents in order to study pores and patterns of cell growth in a non-disruptive manner via X-ray computed microtomography (micro-CT). After the comparison of multiple contrast agents, a 3% aqueous phosphotungstic acid solution in distilled water was identified as the most effective amongst the media, requiring 24 h of incubation. The differences in intensity values between collagen fibers, pores, and masses of cells allow for the accurate segmentation needed for further analysis. Moreover, the presented protocol allows visualization of porous collagen scaffolds under aqueous conditions, which is crucial for the multimodal study of the native structure of samples.