Composition for treating ischemic diseases or neurogenic inflammation, containing, as active ingredient, neural progenitor cells or secretome thereof
A technology for neural precursor cells and ischemic diseases, which can be used in medical preparations containing active ingredients, nervous system cells, cardiovascular system diseases, etc. Effects on number and microvascular concentration
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Embodiment 1
[0078] Example 1. The therapeutic effect of polysialic acid neural cell adhesion molecule-positive neural precursor cells on ischemic diseases and neuroinflammatory diseases
[0079] experimental method
[0080] NPC derived from human mesenchymal stem cells and human embryonic stem cells PSA-NCAM+ Cell Culture and Differentiation
[0081] The use of human cells was approved by the Institutional Review Board (IRB No. 4-2008-0643). Human bone marrow was harvested from the posterior iliac crest of healthy adult volunteers who gave informed consent. The acquisition method is briefly explained as follows, that is, bone marrow mononuclear cells are separated by density gradient centrifugation (GE Healthcare, Uppsala, Sweden), and the bone marrow is placed in DMEM fed with 10% fasting blood sugar (FBS) (Gibco, Grand Island, NY). After monocytes are incubated at a temperature of 37 °C in an atmosphere containing 5% CO 2 cultured in humidified air. After 24 hours, wash and remove ...
Embodiment 2
[0122] Example 2. The therapeutic effect of ischemic diseases and neuroinflammatory diseases targeting the secretome of neural precursor cells
[0123] Experimental materials and experimental methods
[0124] NPCs derived from human embryonic stem cells PSA-NCAM+ Acquisition of cells
[0125] The use of human cells was approved by the Institutional Review Board (IRB No. 4-2008-0643). For neural induction, on human embryonic stem cell medium (Invitrogen) without basic fibroblast growth factor, in the presence of 5 μM free base (Sigma, St. Louis, MO) and 5-10 μM SB431542 (Calbiochem, SanDiego, CA) suspension cultured various embryoid bodies (embryoid bodies, EBs) derived from human embryonic stem cells and iPSCs for 4 days, after inputting The 1XN2 (Invitrogen) medium of basic fibroblast growth factor was adsorbed on matrigel-coated culture dishes (BD Biosciences, Bedford, MA) for about 5 days (Kim, D.S., Lee, D.R., Kim, H.S., et al. al. (2012). Highly pure and expandable PS...
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