Figure 1.
Figure 1. Schematic representation of the model concept for a chimeric situation. Cellular development within the stem cell compartment (left) is characterized by the possibility of individual cells (black and white circles) to reside in 2 different growth environments (GE-A, gray; GE-Ω, white). The affinity (a) of cells to reside in GE-A can reversibly change depending on the actual GE (gain in GE-A, loss in GE-Ω). The processes of a-loss/gain and of transition between the 2 growth environments (characterized by the model parameters d, r, and fα, fω, respectively) are assumed to be strain specific, illustrated by the D2/B6 superscripts. The same holds for the process of proliferation (amplification due to cell division), which is described by the average generation time τc. Cells that have lost the potential to change to GE-A and, therefore to regain a (denoted as differentiated cells), will pass through different precursor stages to become mature leukocytes. Regulation processes of precursor and mature cell stages are neglected in the current model version.

Schematic representation of the model concept for a chimeric situation. Cellular development within the stem cell compartment (left) is characterized by the possibility of individual cells (black and white circles) to reside in 2 different growth environments (GE-A, gray; GE-Ω, white). The affinity (a) of cells to reside in GE-A can reversibly change depending on the actual GE (gain in GE-A, loss in GE-Ω). The processes of a-loss/gain and of transition between the 2 growth environments (characterized by the model parameters d, r, and fα, fω, respectively) are assumed to be strain specific, illustrated by the D2/B6 superscripts. The same holds for the process of proliferation (amplification due to cell division), which is described by the average generation time τc. Cells that have lost the potential to change to GE-A and, therefore to regain a (denoted as differentiated cells), will pass through different precursor stages to become mature leukocytes. Regulation processes of precursor and mature cell stages are neglected in the current model version.

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