|Publication Type||Journal Article|
|Year of Publication||2017|
|Authors||Tripathi, P, Rodriguez-Muela, N, Klim, JR, A de Boer, S, Agrawal, S, Sandoe, J, Lopes, CS, Ogliari, KSassi, Williams, LA, Shear, M, Rubin, LL, Eggan, K, Zhou, Q|
|Journal||Stem Cell Reports|
|Date Published||2017 Aug 08|
Amyotrophic lateral sclerosis (ALS) is a fatal and rapidly progressing motor neuron disease. Astrocytic factors are known to contribute to motor neuron degeneration and death in ALS. However, the role of astrocyte in promoting motor neuron protein aggregation, a disease hallmark of ALS, remains largely unclear. Here, using culture models of human motor neurons and primary astrocytes of different genotypes (wild-type or SOD1 mutant) and reactive states (non-reactive or reactive), we show that reactive astrocytes, regardless of their genotypes, reduce motor neuron health and lead to moderate neuronal loss. After prolonged co-cultures of up to 2 months, motor neurons show increased axonal and cytoplasmic protein inclusions characteristic of ALS. Reactive astrocytes induce protein aggregation in part by releasing transforming growth factor β1 (TGF-β1), which disrupts motor neuron autophagy through the mTOR pathway. These results reveal the important contribution of reactive astrocytes in promoting aspects of ALS pathology independent of genetic influences.
|Alternate Journal||Stem Cell Reports|
|PubMed Central ID||PMC5549875|