Перегляд вихідного коду сторінки Notch Signaling Neuronal Differentiation

Investigation of gene expression by quantitative RT-PCR comparing three dimensional cultures with cells from planar surfaces revealed that the keratinocytes both alone and along with fibroblasts up-regulated Dll-4 expression significantly (p[http://www.ncbi.nlm.nih.gov/pubmed/16574785 16574785] kDa band and actin (40 kDa band) was used for normalization (Figure 6D).TREC analysisTo further confirm the in vitro commitment of the progenitors used to the T cell lineage we analysed TREC levels in both an aliquot of cord blood CD34+ cells seeded into the skin construct and some CD3 cells generated from these after 10 days of co-culture. Our results from three independent experiments revealed a band corresponding to the TREC amplicon observed only from newly generated T cells and not from the original population of seeding cells. Moreover we quantified TREC levels from both CD3 cells generated from the skin systems and separated from cord blood and the concentration resulted to be 1.51?0.16 per new generated cell and 0.39?0.09 per cord peripheral T cell (p [http://www.ncbi.nlm.nih.gov/pubmed/ 23727046   23727046] in the CD34 cells subsets composition.doi: 10.1371/journal.pone.0069572.gmatrix system. In all the conditions tested the adult CD34+ cells died within the first 72 hours of culture [http://www.medchemexpress.com/MG-132.html order 133407-82-6] whereas the cord blood progenitors actively proliferated and generated thymocytes. All the cultures were maintained for up to two weeks. Our phenotypic analysis of the cells from either source showed distinct differences. In adult blood 88 ?4   CD34 cells were CD38 versus 63 ?3   in cord blood (p