Near- infrared nanosensors enable optical imaging of oxytocin with selectivity over vasopressin in acute mouse brain slices
成果类型:
Article
署名作者:
Mun, Jaewan; Navarro, Nicole; Jeong, Sanghwa; Ouassil, Nicholas; Leem, Esther; Beyene, Abraham G.; Landry, Markita P.; Murphy, Catherine
署名单位:
University of California System; University of California Berkeley; University of California System; University of California Berkeley; University of California System; University of California Berkeley; Pusan National University; Howard Hughes Medical Institute; Chan Zuckerberg Initiative (CZI)
刊物名称:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
ISSN/ISSBN:
0027-10244
DOI:
10.1073/pnas.2314795121
发表日期:
2024-06-25
关键词:
thyrotropin-releasing-hormone
electrical-stimulation
paraventricular nucleus
cerebrospinal-fluid
male-rats
dopamine
receptor
binding
plasma
modulation
摘要:
Oxytocin plays a critical role in regulating social behaviors, yet our understanding of its function in both neurological health and disease remains incomplete. Real - time oxytocin imaging probes with spatiotemporal resolution relevant to its endogenous signaling are required to fully elucidate oxytocin's role in the brain. Herein, we describe a nearinfrared oxytocin nanosensor (nIROXT), a synthetic probe capable of imaging oxytocin in the brain without interference from its structural analogue, vasopressin. nIROXT leverages the inherent tissue - transparent fluorescence of single - walled carbon nanotubes (SWCNT) and the molecular recognition capacity of an oxytocin receptor peptide fragment to selectively and reversibly image oxytocin. We employ these nanosensors to monitor electrically stimulated oxytocin release in brain tissue, revealing oxytocin release sites with a median size of 3 i.t m in the paraventricular nucleus of C57BL/6 mice, which putatively represents the spatial diffusion of oxytocin from its point of release. These data demonstrate that covalent SWCNT constructs, such as nIROXT, are powerful optical tools that can be leveraged to measure neuropeptide release in brain tissue.