mTORC1 in classical monocytes: Links to human size variation and neuropsychiatric disease

mTORC1 in classical monocytes: Links to human size variation and neuropsychiatric disease
published in Aging.

In this new study, researchers Karl Berner, Naci Oz, Alaattin Kaya, Animesh Acharjee, and Jon Berner from Woodinville Psychiatric Associates, Virginia Commonwealth University, University of Birmingham, University Hospitals Birmingham, and MRC Health Data Research UK, aimed to measure phosphorylated p70S6K, a marker for mTORC1 activity, in individuals with psychiatric disease to determine whether phosphorylated p70S6K could predict medication response.






Their results showed that mTORC1 activity correlated highly with classical biometrics (height, macrocephaly, pupil distance) and specific neuropsychiatric disease profiles (anxiety and autism).

“Our suggest that human variability of mTORC1 gain of function observed during the differentiation of stem-like monocytes into vascular tissue-resident macrophages correlates with physical size, subsets of , and clinical ketamine or rapamycin response,” the researchers state.

More information:
Karl Berner et al, mTORC1 activation in presumed classical monocytes: observed correlation with human size variation and neuropsychiatric disease, Aging (2024). DOI: 10.18632/aging.206033

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mTORC1 in classical monocytes: Links to human size variation and neuropsychiatric disease (2024, August 7)
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