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Engineering water exchange is a safe and effective method for magnetic resonance imaging in diverse cell types

Authors :
Miller, Austin DC
Miller, Austin DC
Chowdhury, Soham P
Hanson, Hadley W
Linderman, Sarah K
Ghasemi, Hannah I
Miller, Wyatt D
Morrissey, Meghan A
Richardson, Chris D
Gardner, Brooke M
Mukherjee, Arnab
Miller, Austin DC
Miller, Austin DC
Chowdhury, Soham P
Hanson, Hadley W
Linderman, Sarah K
Ghasemi, Hannah I
Miller, Wyatt D
Morrissey, Meghan A
Richardson, Chris D
Gardner, Brooke M
Mukherjee, Arnab
Source :
Journal of Biological Engineering; vol 18, iss 1, 30; 1754-1611
Publication Year :
2024

Abstract

Aquaporin-1 (Aqp1), a water channel, has garnered significant interest for cell-based medicine and in vivo synthetic biology due to its ability to be genetically encoded to produce magnetic resonance signals by increasing the rate of water diffusion in cells. However, concerns regarding the effects of Aqp1 overexpression and increased membrane diffusivity on cell physiology have limited its widespread use as a deep-tissue reporter. In this study, we present evidence that Aqp1 generates strong diffusion-based magnetic resonance signals without adversely affecting cell viability or morphology in diverse cell lines derived from mice and humans. Our findings indicate that Aqp1 overexpression does not induce ER stress, which is frequently associated with heterologous expression of membrane proteins. Furthermore, we observed that Aqp1 expression had no detrimental effects on native biological activities, such as phagocytosis, immune response, insulin secretion, and tumor cell migration in the analyzed cell lines. These findings should serve to alleviate any lingering safety concerns regarding the utilization of Aqp1 as a genetic reporter and should foster its broader application as a noninvasive reporter for in vivo studies.

Details

Database :
OAIster
Journal :
Journal of Biological Engineering; vol 18, iss 1, 30; 1754-1611
Notes :
application/pdf, Journal of Biological Engineering vol 18, iss 1, 30 1754-1611
Publication Type :
Electronic Resource
Accession number :
edsoai.on1449594624
Document Type :
Electronic Resource