Harnessing three-dimensional (3D) cell culture models for pulmonary infections: State of the art and future directions

• Published in: Naunyn-Schmiedeberg's archives of pharmacology Vol. 396; no. 11; pp. 2861 - 2880
• Main Authors: Shah, Disha D., Raghani, Neha R., Chorawala, Mehul R., Singh, Sudarshan, Prajapati, Bhupendra G.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.11.2023; Springer Nature B.V
• Subjects: Animal models; Animals; Biomedical and Life Sciences; Biomedicine; Cell culture; Cell Culture Techniques - methods; Cell interactions; COVID-19; Embryo cells; Infections; Kidneys; Lung; Mammals; Morbidity; Neurosciences; Organoids; Pharmacology/Toxicology; Pluripotency; Respiratory syncytial virus; Respiratory tract infection; Review; SARS-CoV-2; Severe acute respiratory syndrome coronavirus 2; Structure-function relationships; Vaccine development; Pulmonary infections; SARS-CoV-2; Organoids; 2D cell culture; Respiratory viruses; 3D cell culture; Spheroids
• ISSN: 0028-1298; 1432-1912
• DOI: 10.1007/s00210-023-02541-2

Pulmonary infections have been a leading etiology of morbidity and mortality worldwide. Upper and lower respiratory tract infections have multifactorial causes, which include bacterial, viral, and rarely, fungal infections. Moreover, the recent emergence of SARS-CoV-2 has created havoc and imposes a huge healthcare burden. Drug and vaccine development against these pulmonary pathogens like respiratory syncytial virus, SARS-CoV-2, Mycobacteria , etc., requires a systematic set of tools for research and investigation. Currently, in vitro 2D cell culture models are widely used to emulate the in vivo physiologic environment. Although this approach holds a reasonable promise over pre-clinical animal models, it lacks the much-needed correlation to the in vivo tissue architecture, cellular organization, cell-to-cell interactions, downstream processes, and the biomechanical milieu. In view of these inadequacies, 3D cell culture models have recently acquired interest. Mammalian embryonic and induced pluripotent stem cells may display their remarkable self-organizing abilities in 3D culture, and the resulting organoids replicate important structural and functional characteristics of organs such the kidney, lung, gut, brain, and retina. 3D models range from scaffold-free systems to scaffold-based and hybrid models as well. Upsurge in organs-on-chip models for pulmonary conditions has anticipated encouraging results. Complexity and dexterity of developing 3D culture models and the lack of standardized working procedures are a few of the setbacks, which are expected to be overcome in the coming times. Herein, we have elaborated the significance and types of 3D cell culture models for scrutinizing pulmonary infections, along with the in vitro techniques, their applications, and additional systems under investigation. Graphical Abstract