TY - JOUR
T1 - MTOR plays an important role in cow's milk allergy-associated behavioral and immunological deficits
AU - Wu, Jiangbo
AU - De Theije, Caroline M G
AU - Da Silva, Sofia Lopes
AU - Van Der Horst, Hilma
AU - Reinders, Margot T M
AU - Broersen, Laus M.
AU - Willemsen, Linette E M
AU - Kas, Martien J H
AU - Garssen, Johan
AU - Kraneveld, Aletta D.
PY - 2015/6/27
Y1 - 2015/6/27
N2 - Autism spectrum disorder (ASD) is multifactorial, with both genetic as well as environmental factors working in concert to develop the autistic phenotype. Immunological disturbances in autistic individuals have been reported and a role for food allergy has been suggested in ASD. Single gene mutations in mammalian target of rapamycin (mTOR) signaling pathway are associated with the development of ASD and enhanced mTOR signaling plays a central role in directing immune responses towards allergy as well. Therefore, the mTOR pathway may be a pivotal link between the immune disturbances and behavioral deficits observed in ASD. In this study it was investigated whether the mTOR pathway plays a role in food allergy-induced behavioral and immunological deficits. Mice were orally sensitized and challenged with whey protein. Meanwhile, cow's milk allergic (CMA) mice received daily treatment of rapamycin. The validity of the CMA model was confirmed by showing increased allergic immune responses. CMA mice showed reduced social interaction and increased repetitive self-grooming behavior. Enhanced mTORC1 activity was found in the brain and ileum of CMA mice. Inhibition of mTORC1 activity by rapamycin improved the behavioral and immunological deficits of CMA mice. This effect was associated with increase of Treg associated transcription factors in the ileum of CMA mice. These findings indicate that mTOR activation may be central to both the intestinal, immunological, and psychiatric ASD-like symptoms seen in CMA mice. It remains to be investigated whether mTOR can be seen as a therapeutic target in cow's milk allergic children suffering from ASD-like symptoms.
AB - Autism spectrum disorder (ASD) is multifactorial, with both genetic as well as environmental factors working in concert to develop the autistic phenotype. Immunological disturbances in autistic individuals have been reported and a role for food allergy has been suggested in ASD. Single gene mutations in mammalian target of rapamycin (mTOR) signaling pathway are associated with the development of ASD and enhanced mTOR signaling plays a central role in directing immune responses towards allergy as well. Therefore, the mTOR pathway may be a pivotal link between the immune disturbances and behavioral deficits observed in ASD. In this study it was investigated whether the mTOR pathway plays a role in food allergy-induced behavioral and immunological deficits. Mice were orally sensitized and challenged with whey protein. Meanwhile, cow's milk allergic (CMA) mice received daily treatment of rapamycin. The validity of the CMA model was confirmed by showing increased allergic immune responses. CMA mice showed reduced social interaction and increased repetitive self-grooming behavior. Enhanced mTORC1 activity was found in the brain and ileum of CMA mice. Inhibition of mTORC1 activity by rapamycin improved the behavioral and immunological deficits of CMA mice. This effect was associated with increase of Treg associated transcription factors in the ileum of CMA mice. These findings indicate that mTOR activation may be central to both the intestinal, immunological, and psychiatric ASD-like symptoms seen in CMA mice. It remains to be investigated whether mTOR can be seen as a therapeutic target in cow's milk allergic children suffering from ASD-like symptoms.
KW - Autism spectrum disorder (ASD)
KW - Cow's milk allergy (CMA)
KW - Mammalian target of rapamycin (mTOR)
KW - Rapamycin
KW - Regulatory T (Treg) cells
UR - http://www.scopus.com/inward/record.url?scp=84933036410&partnerID=8YFLogxK
U2 - 10.1016/j.neuropharm.2015.04.035
DO - 10.1016/j.neuropharm.2015.04.035
M3 - Article
C2 - 26027949
AN - SCOPUS:84933036410
SN - 0028-3908
VL - 97
SP - 220
EP - 232
JO - Neuropharmacology
JF - Neuropharmacology
ER -