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Ziegler, K.A.* ; Ahles, A.* ; Dueck, A.* ; Esfandyari, D.* ; Pichler, P.* ; Weber, K.* ; Kotschi, S.* ; Bartelt, A. ; Sinicina, I.* ; Graw, M.* ; Leonhardt, H.* ; Weckbach, L.T.* ; Massberg, S.* ; Schifferer, M.* ; Simons, M.* ; Höher, L. ; Luo ; Ertürk, A. ; Schiattarella, G.G.* ; Sassi, Y.* ; Misgeld, T.* ; Engelhardt, S.*

Immune-mediated denervation of the pineal gland underlies sleep disturbance in cardiac disease.

Science 381, 285-290 (2023)
Verlagsversion DOI PMC
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Disruption of the physiologic sleep-wake cycle and low melatonin levels frequently accompany cardiac disease, yet the underlying mechanism has remained enigmatic. Immunostaining of sympathetic axons in optically cleared pineal glands from humans and mice with cardiac disease revealed their substantial denervation compared with controls. Spatial, single-cell, nuclear, and bulk RNA sequencing traced this defect back to the superior cervical ganglia (SCG), which responded to cardiac disease with accumulation of inflammatory macrophages, fibrosis, and the selective loss of pineal gland-innervating neurons. Depletion of macrophages in the SCG prevented disease-associated denervation of the pineal gland and restored physiological melatonin secretion. Our data identify the mechanism by which diurnal rhythmicity in cardiac disease is disturbed and suggest a target for therapeutic intervention.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Superior Cervical-ganglion; Expression; Transgene; Melatonin; Neurons; Atrial
Sprache englisch
Veröffentlichungsjahr 2023
HGF-Berichtsjahr 2023
ISSN (print) / ISBN 0036-8075
e-ISSN 1095-9203
Zeitschrift Science
Quellenangaben Band: 381, Heft: 6655, Seiten: 285-290 Artikelnummer: , Supplement: ,
Verlag American Association for the Advancement of Science (AAAS)
Verlagsort 1200 New York Ave, Nw, Washington, Dc 20005 Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Diabetes and Cancer (IDC)
Institute for Tissue Engineering and Regenerative Medicine (ITERM)
POF Topic(s) 90000 - German Center for Diabetes Research
30205 - Bioengineering and Digital Health
Forschungsfeld(er) Helmholtz Diabetes Center
Enabling and Novel Technologies
PSP-Element(e) G-501900-251
G-505800-001
Förderungen TUM
European Research Council
Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)
DZHK (German Centre for Cardiovascular Research)
DFG
German Cardiac Society
Munich Center for Systems Neurology
ERC under the European Union
German Center for Neurodegenerative Diseases (DZNE)
BMBF
DOI 10.1126/science.abn6366
WOS ID 001046763100024
Scopus ID 85165488796
PubMed ID 37471539
Erfassungsdatum 2023-10-06
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