Fugetaxis of Cell-in-Catalytic-Coat Nanobiohybrids in Glucose Gradients

Authors
Rheem, Hyeong BinChoi, HyunwooYang, SeoinHan, SolRhee, Su YeonJeong, HyeongseopLee, Kyung-BokLee, YejiKim, In-SanLee, HojaeChoi, Insung S. S.
Issue Date
2023-10
Publisher
Wiley - V C H Verlag GmbbH & Co.
Citation
Small, v.19, no.41
Abstract
Manipulation and control of cell chemotaxis remain an underexplored territory despite vast potential in various fields, such as cytotherapeutics, sensors, and even cell robots. Herein is achieved the chemical control over chemotactic movement and direction of Jurkat T cells, as a representative model, by the construction of cell-in-catalytic-coat structures in single-cell nanoencapsulation. Armed with the catalytic power of glucose oxidase (GOx) in the artificial coat, the nanobiohybrid cytostructures, denoted as Jurkat([Lipo_GOx]), exhibit controllable, redirected chemotactic movement in response to d-glucose gradients, in the opposite direction to the positive-chemotaxis direction of naive, uncoated Jurkat cells in the same gradients. The chemically endowed, reaction-based fugetaxis of Jurkat([Lipo_GOx]) operates orthogonally and complementarily to the endogenous, binding/recognition-based chemotaxis that remains intact after the formation of a GOx coat. For instance, the chemotactic velocity of Jurkat([Lipo_GOx]) can be adjusted by varying the combination of d-glucose and natural chemokines (CXCL12 and CCL19) in the gradient. This work offers an innovative chemical tool for bioaugmenting living cells at the single-cell level through the use of catalytic cell-in-coat structures.
Keywords
VASCULAR SMOOTH-MUSCLE; SIGNALING PATHWAYS; CHEMOTAXIS; MIGRATION; RECEPTOR; CXCL12; ACTIVATION; MOVEMENT; MOTILITY; CCL19; catalysis; chemokines; chemotaxis; liposomes; single-cell nanoencapsulation
ISSN
1613-6810
URI
https://pubs.kist.re.kr/handle/201004/113248
DOI
10.1002/smll.202301431
Appears in Collections:
KIST Article > 2023
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