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Item Can Salivary Innate Immune Molecules Provide Clue on Taste Dysfunction in COVID-19?(Frontiers, 2021-10) Ermel, Aaron; Thyvalikakath, Thankam Paul; Foroud, Tatiana; Khan, Babar; Srinivasan, Mythily; Medicine, School of MedicineEmerging concerns following the severe acute respiratory syndrome coronavirus-2 (SARS-CoV2) pandemic are the long-term effects of coronavirus disease (COVID)-19. Dysgeusia in COVID-19 is supported by the abundant expression of the entry receptor, angiotensin-converting enzyme-2 (ACE2), in the oral mucosa. The invading virus perturbs the commensal biofilm and regulates the host responses that permit or suppress viral infection. We correlated the microbial recognition receptors and soluble ACE2 (sACE2) with the SARS-CoV2 measures in the saliva of COVID-19 patients. Data indicate that the toll-like receptor-4, peptidoglycan recognition protein, and sACE2 are elevated in COVID-19 saliva and correlate moderately with the viral load.Item Osteoglophonic dysplasia: A ‘common’ mutation in a rare disease(Wiley Online Library, 2010-08) Sow, AJ; Ramli, R.; Latiff, ZA; Ichikawa, S.; Gray, AK; Nordin, R.; Abd Jabar, MN; Primuharsa Putra, SHA; Siar, CH; Econs, MJ; Department of Medicine, IU School of MedicineItem A Proximal Culture Method to Study Paracrine Signaling Between Cells(MyJove Corporation, 2018-08-28) Dasari, Subramanyam; Pandhiri, Taruni; Haley, James; Lenz, Dean; Mitra, Anirban K.; Medical and Molecular Genetics, School of MedicineIntercellular interactions play an important role in many biological processes, including tumor progression, immune responses, angiogenesis, and development. Paracrine or juxtacrine signaling mediates such interactions. The use of a conditioned medium and coculture studies are the most common methods to discriminate between these two types of interactions. However, the effect of localized high concentrations of secreted factors in the microenvironment during the paracrine interactions is not accurately recapitulated by conditioned medium and, thus, may lead to imprecise conclusions. To overcome this problem, we have devised a proximal culture method to study paracrine signaling. The two cell types are grown on either surface of a 10 µm-thick polycarbonate membrane with 0.4 µm pores. The pores allow the exchange of secreted factors and, at the same time, inhibit juxtacrine signaling. The cells can be collected and lysed at the endpoint to determine the effects of the paracrine signaling. In addition to allowing for localized concentration gradients of secreted factors, this method is amenable to experiments involving prolonged periods of culture, as well as the use of inhibitors. While we use this method to study the interactions between ovarian cancer cells and the mesothelial cells they encounter at the site of metastasis, it can be adapted to any two adherent cell types for researchers to study paracrine signaling in various fields, including tumor microenvironment, immunology, and development.