We isolate them through low-stress dissociation optimized for stromal preservation, followed by marker-based enrichment for CD45, CD11b, and MHC-II. Functional screens validate cytokine responsiveness and antigen-presentation profiles, ensuring they reflect the CP stroma's specialized immune surveillance role relevant to CSF barrier research.
Yes. Their preserved inflammatory-response behavior and barrier-associated signaling make them suitable for modeling age-linked CP dysfunction, including altered cytokine secretion, diminished antigen-presentation efficiency, and impaired CSF immune filtration. They provide a relevant platform for mechanistic studies on neuroimmune aging.
Yes. Their stromal origin equips them to tolerate physiological shear levels. We verify performance under controlled flow conditions, confirming stable morphology and preserved cytokine responsiveness, making them ideal for advanced CSF-chip systems or dynamic barrier-interaction studies.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.