TY - JOUR
T1 - Delivering DNA Aptamers Across the Blood-Brain Barrier Reveals Heterogeneous Decreased ATP in Different Brain Regions of Alzheimer’s Disease Mouse Models
AU - Banik, Mandira
AU - Ledray, Aaron P.
AU - Wu, Yuting
AU - Lu, Yi
N1 - This material is based on work supported by the US National Institute of Health (GM141931 to Y.L.) and the Allen Distinguished Investigator Award (to Y.L.), a Paul G. Allen Frontiers Group advised grant of the Paul G. Allen Family Foundation. M.B. is supported by NIH Chemistry-Biology Interface Training Grant at the University of Illinois Urbana\u2013Champaign (T32GM136629) and the NSF Graduate Research Fellowship. We also thank the Welch Foundation (grant F-0020) for supporting the Y.L. group research. The images in this work were collected at the Biomedical Imaging Center (RRID: SCR_021898) and the Microscopy and Imaging Facility (RRID: SCR_021756), core facilities within the Center for Biomedical Research Support at the University of Texas at Austin.
PY - 2024/8/28
Y1 - 2024/8/28
N2 - DNA aptamers have been developed as sensors to detect metabolites with high sensitivity, selectivity, and biocompatibility. While they are effective in sensing important targets in the brain, the lack of methods for their efficient delivery across the blood-brain barrier (BBB) has significantly hindered their applications in brain research. To address this issue, we herein report the development of brain cell-derived exosomes as endogenous BBB delivery vehicles to deliver an ATP-responsive aptamer across the BBB of live mice for noninvasive live brain imaging. We found that the system uses endosome recycling to transfer the sensors between the delivered exosomes and native recycling endosomes, resulting in high delivery efficiencies. Using this system, we observed unique signal distributions for ATP across different brain regions, with significant accumulation in the subiculum and cortex in healthy mice. In an Alzheimer’s disease transgenic mouse model, ATP levels decreased in the subiculum and cortex, demonstrating this method’s capability to determine metabolite location and relative abundance with high spatial resolution in vivo. Since DNA aptamers have been obtained for many other targets, the method developed in this work can be applied to deliver sensors across the BBB to image a wide range of other brain-related metabolites.
AB - DNA aptamers have been developed as sensors to detect metabolites with high sensitivity, selectivity, and biocompatibility. While they are effective in sensing important targets in the brain, the lack of methods for their efficient delivery across the blood-brain barrier (BBB) has significantly hindered their applications in brain research. To address this issue, we herein report the development of brain cell-derived exosomes as endogenous BBB delivery vehicles to deliver an ATP-responsive aptamer across the BBB of live mice for noninvasive live brain imaging. We found that the system uses endosome recycling to transfer the sensors between the delivered exosomes and native recycling endosomes, resulting in high delivery efficiencies. Using this system, we observed unique signal distributions for ATP across different brain regions, with significant accumulation in the subiculum and cortex in healthy mice. In an Alzheimer’s disease transgenic mouse model, ATP levels decreased in the subiculum and cortex, demonstrating this method’s capability to determine metabolite location and relative abundance with high spatial resolution in vivo. Since DNA aptamers have been obtained for many other targets, the method developed in this work can be applied to deliver sensors across the BBB to image a wide range of other brain-related metabolites.
UR - https://www.scopus.com/pages/publications/85200371499
UR - https://www.scopus.com/inward/citedby.url?scp=85200371499&partnerID=8YFLogxK
U2 - 10.1021/acscentsci.4c00563
DO - 10.1021/acscentsci.4c00563
M3 - Article
C2 - 39220690
AN - SCOPUS:85200371499
SN - 2374-7943
VL - 10
SP - 1585
EP - 1593
JO - ACS Central Science
JF - ACS Central Science
IS - 8
ER -