Single-Cell Detection of Secreted Aβ and sAPPα from Human IPSC-Derived Neurons and Astrocytes.
Mei-Chen LiaoChristina R MuratoreTodd M GierahnSarah E SullivanPriya SrikanthPhilip L De JagerJ Christopher LoveTracy L Young-PearsePublished in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2016)
We have established a technology that, for the first time, detects secreted analytes from single human neurons and astrocytes. We examine secretion of the Alzheimer's disease-relevant factors amyloid β (Aβ) and soluble amyloid precursor protein-alpha (sAPPα) and present novel findings that could not have been observed without a single-cell analytical platform. First, we identify a previously unappreciated subpopulation that secretes high levels of Aβ in the absence of detectable sAPPα. Further, we show that multiple cell types secrete high levels of Aβ and sAPPα, but cells expressing GABAergic neuronal markers are overrepresented. Finally, we show that astrocytes are competent to secrete high levels of Aβ and therefore may be a significant contributor to Aβ accumulation in the brain.
Keyphrases
- single cell
- endothelial cells
- rna seq
- induced pluripotent stem cells
- high throughput
- spinal cord
- induced apoptosis
- cerebral ischemia
- cognitive decline
- stem cells
- oxidative stress
- signaling pathway
- mesenchymal stem cells
- protein protein
- loop mediated isothermal amplification
- mild cognitive impairment
- amino acid
- blood brain barrier
- mass spectrometry
- resting state
- bone marrow
- quantum dots
- wild type