Conditioned medium from the stem cells of human dental pulp improves cognitive function in a mouse model of Alzheimer’s disease
•Intranasal administration of SHED-CM improves cognition in a mouse model of AD.•SHED-CM converts the pro-inflammatory AD environment to an anti-inflammatory one.•SHED-CM induces the accumulation of M2 microglia in the mouse AD brain.•SHEDs secrete multiple factors beneficial for the treatment of AD...
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Veröffentlicht in: | Behavioural brain research 2015-10, Vol.293, p.189-197 |
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Sprache: | eng |
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Zusammenfassung: | •Intranasal administration of SHED-CM improves cognition in a mouse model of AD.•SHED-CM converts the pro-inflammatory AD environment to an anti-inflammatory one.•SHED-CM induces the accumulation of M2 microglia in the mouse AD brain.•SHEDs secrete multiple factors beneficial for the treatment of AD.
Alzheimer’s disease (AD) is a progressive, neurodegenerative disease characterized by a decline in cognitive abilities and the appearance of β-amyloid plaques in the brain. Although the pathogenic mechanisms associated with AD are not fully understood, activated microglia releasing various neurotoxic factors, including pro-inflammatory cytokines and oxidative stress mediators, appear to play major roles. Here, we investigated the therapeutic benefits of a serum-free conditioned medium (CM) derived from the stem cells of human exfoliated deciduous teeth (SHEDs) in a mouse model of AD. The intranasal administration of SHEDs in these mice resulted in substantially improved cognitive function. SHED-CM contained factors involved in multiple neuroregenerative mechanisms, such as neuroprotection, axonal elongation, neurotransmission, the suppression of inflammation, and microglial regulation. Notably, SHED-CM attenuated the pro-inflammatory responses induced by β-amyloid plaques, and generated an anti-inflammatory/tissue-regenerating environment, which was accompanied by the induction of anti-inflammatory M2-like microglia. Our data suggest that SHED-CM may provide significant therapeutic benefits for AD. |
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ISSN: | 0166-4328 1872-7549 |
DOI: | 10.1016/j.bbr.2015.07.043 |