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In (B ), the ratio between the division indexes of wild-type (B6) and MHC-II KO lymph node transplant recovered CD4+Foxp3+ Tregs and CD4+Foxp3− conventional T cells is shown.
The cell division indexes in SLE T cells stimulated with anti-CD3/CD28 plus control IgG and with anti-CD3/CD28 plus anti-CD200R1 attibody at 20 ng/ml or 100 ng/ml were 0.87 ± 0.54, 1.43 ± 0.92, and 2.34 ± 1.85, respectively (P < 0.05).
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The division index of proliferated cultures was derived by the formula: Division Index = (Proliferation Index)×(Percent Divided), where the proliferation index is the average number of cell divisions of the responder cells.
Therefore, this number serves as the division index for the VLC case.
In the FLC case, there is only one table and the division index is zero.
These included patch density (PD), edge density (ED), landscape division index (DIVISION), contagion (CONTAG), Shannon's evenness index (SHEI), and Shannon's diversity index (SHDI).
Correlations were identified between indicators of cash crop expansion (total area and total production of cash crops) and a family of landscape fragmentation metrics (patch density, edge density, landscape division index, effective mesh size, splitting index, Shannon's diversity index, and aggregation index).
The software was used to calculate percent divided, as well as division index.
The division history of CD4+CD90.2+CD45.1+CD45.2−7AAD− responder cells was analyzed using Flowjo v8.8.6 (TreeStar, Stanford, US) and the division index (mean divisions per divided cell) plotted.
For FACS based suppression assays, proliferation was calculated by division index (DI), with suppression calculated as previously described [24].
The division index represents the average number of cell divisions of all cells in the population (i.e. it includes the undivided cells).
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