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Sökning: id:"swepub:oai:lup.lub.lu.se:66eeaed9-0ac9-44f3-a57c-59063c6eb143" > Combining CRISPR-Ca...

Combining CRISPR-Cas9 and brain imaging to study the link from genes to molecules to networks

Marciano, Sabina (författare)
University of Tübingen
Ionescu, Tudor M. (författare)
University of Tübingen
Saw, Ran Sing (författare)
University of Tübingen
visa fler...
Cheong, Rachel Y. (författare)
Lund University,Lunds universitet,Brain Repair and Imaging in Neural Systems (BRAINS),Forskargrupper vid Lunds universitet,Lund University Research Groups
Kirik, Deniz (författare)
Lund University,Lunds universitet,Brain Repair and Imaging in Neural Systems (BRAINS),Forskargrupper vid Lunds universitet,Lund University Research Groups
Maurer, Andreas (författare)
University of Tübingen
Pichler, Bernd J. (författare)
University of Tübingen
Herfert, Kristina (författare)
University of Tübingen
visa färre...
 (creator_code:org_t)
2022-09-26
2022
Engelska.
Ingår i: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 0027-8424. ; 119:40
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Receptors, transporters, and ion channels are important targets for therapy development in neurological diseases, but their mechanistic role in pathogenesis is often poorly understood. Gene editing and in vivo imaging approaches will help to identify the molecular and functional role of these targets and the consequence of their regional dysfunction on the whole-brain level. We combine CRISPR-Cas9 gene editing with in vivo positron emission tomography (PET) and functional MRI (fMRI) to investigate the direct link between genes, molecules, and the brain connectome. The extensive knowledge of the Slc18a2 gene encoding the vesicular monoamine transporter (VMAT2), involved in the storage and release of dopamine, makes it an excellent target for studying the gene network relationships while structurally preserving neuronal integrity and function. We edited the Slc18a2 in the substantia nigra pars compacta of adult rats and used in vivo molecular imaging besides behavioral, histological, and biochemical assessments to characterize the CRISPR-Cas9–mediated VMAT2 knockdown. Simultaneous PET/fMRI was performed to investigate molecular and functional brain alterations. We found that stage-specific adaptations of brain functional connectivity follow the selective impairment of presynaptic dopamine storage and release. Our study reveals that recruiting different brain networks is an early response to the dopaminergic dysfunction preceding neuronal cell loss. Our combinatorial approach is a tool to investigate the impact of specific genes on brain molecular and functional dynamics, which will help to develop tailored therapies for normalizing brain function.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Nyckelord

CRISPR-Cas9
dopamine
PET
resting-state functional MRI
VMAT2

Publikations- och innehållstyp

art (ämneskategori)
ref (ämneskategori)

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