Schalla, Martha A.Martha A.SchallaOerter, SabrinaSabrinaOerterCubukova, AlevtinaAlevtinaCubukovaMetzger, MarcoMarcoMetzgerAppelt-Menzel, AntjeAntjeAppelt-MenzelStengel, AndreasAndreasStengel2023-09-142023-09-142023-07https://publica.fraunhofer.de/handle/publica/45067210.3390/brainsci13070980Phoenixin-14 is a recently discovered peptide regulating appetite. Interestingly, it is expressed in the gastrointestinal tract; however, its supposed receptor, GPR173, is predominantly found in hypothalamic areas. To date, it is unknown how peripherally secreted phoenixin-14 is able to reach its centrally located receptor. To investigate whether phoenixin is able to pass the blood-brain barrier, we used an in vitro mono-culture blood-brain barrier (BBB) model consisting of brain capillary-like endothelial cells derived from human induced-pluripotent stem cells (hiPSC-BCECs). The passage of 1 nMol and 10 nMol of phoenixin-14 via the mono-culture was measured after 30, 60, 90, 120, 150, 180, 210, and 240 min using a commercial ELISA kit. The permeability coefficients (PC) of 1 nMol and 10 nMol phoenixin-14 were 0.021 ± 0.003 and 0.044 ± 0.013 µm/min, respectively. In comparison with the PC of solutes known to cross the BBB in vivo, those of phoenixin-14 in both concentrations are very low. Here, we show that phoenixin-14 alone is not able to cross the BBB, suggesting that the effects of peripherally secreted phoenixin-14 depend on a co-transport mechanism at the BBB in vivo. The mechanisms responsible for phoenixin-14′s orexigenic property along the gut-brain axis warrant further research.enappetite regulationblood-brain barrierbrain-gut axisgastrointestinal tracthypothalamusin vitro techniquesinduced pluripotent stem cellspeptidesphoenixin-14journal article