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Brain pericytes from stress-susceptible pigs increase blood-brain barrier permeability in vitroKeywords: Blood–brain barrier, Endothelial permeability, Neurovascular unit, Pericytes, Perivascular spaces, Porcine stress syndrome Abstract: In the present work, histological and ultrastructural analyses of brain capillaries from wild type and ryr1 mutated pigs were conducted to investigate the potential impairment of pericytes, in this pathology. In addition, brain pericytes were isolated from the three porcine genotypes (wild-type NN pigs; Nn and nn pigs, bearing one or two (n) mutant ryr1/hal alleles, respectively), and tested in vitro for their influence on the permeability of BBB endothelial monolayers.Enlarged perivascular spaces were observed in ryr1-mutant samples, corresponding to a partial or total detachment of the astrocytic endfeet. These spaces were electron lucent and sometimes filled with lipid deposits and swollen astrocytic feet. At the ultrastructural level, brain pericytes did not seem to be affected because they showed regular morphology and characteristics, so we aimed to check their ability to maintain BBB properties in vitro. Our results indicated that pericytes from the three genotypes of pigs had differing influences on the BBB. Unlike pericytes from NN pigs, pericytes from Nn and nn pigs were not able to maintain low BBB permeability.Electron microscopy observations demonstrated brain capillary modifications in PSS condition, but no change in pericyte morphology. Results from in vitro experiments suggest that brain pericytes from ryr1 mutated pigs, even if they are not affected by this condition at the ultrastructural level, are not able to maintain BBB integrity in comparison with pericytes from wild-type animals.The porcine stress syndrome (PSS) is linked to a single point mutation in the skeletal muscle ryr gene, which leads to the replacement of a cytosine by a thymine molecule at nucleotide 1843 [1]. Upon slaughter, pigs carrying the halothane sensitivity (n) allele at the ryr1 locus can exhibit rapid-onset, severe malignant hyperthermia (MH), experiencing a range of symptoms, including skeletal muscle rigidity, metabolic acidosis, tachycardia and fever, which are due to a
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