Open AccessMATRIX SIMULATION OF DUODENAL CRYPT CELL KINETICS
Author(s) -
Roti Joseph L. Roti,
Dethlefsen Lyle A.
Publication year - 1975
Publication title -
cell proliferation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.647
H-Index - 74
eISSN - 1365-2184
pISSN - 0960-7722
DOI - 10.1111/j.1365-2184.1975.tb01498.x
Subject(s) - crypt , mitosis , cell cycle , compartment (ship) , kinetics , cell division , matrix (chemical analysis) , cell , microfold cell , cell growth , microbiology and biotechnology , chemistry , biophysics , biology , immunology , biochemistry , physics , endocrinology , chromatography , oceanography , quantum mechanics , antigen , geology
The perturbed cellular kinetics of the duodenal crypt following a single injection of hydroxyurea (HU) have been simulated using matrix algebra. Following the direct effects of HU (S‐phase cytotoxicity and a G 1 /S block) the crypt cell kinetics undergo several alterations. Previously documented alterations include: (1) a temporary partial synchronization of the surviving cells, (2) a shortening of the cell‐cycle transit time, and (3) recruitment of normally non‐proliferating cells into active proliferation. These conclusions have been extended by constructing several different complex but theoretically possible recovery models and the validity of each of these models has been evaluated by simulating the following biological data: the number of cells in the S and M‐phase of the cell cycle, total viable cells per crypt, and the per cent labeled mitosis and the number of labeled cells following 3 H‐TdR injections at 9 and 21 hr after HU treatment. The model which showed visually the best overall agreement with all sets of the data was chosen as ‘most probable’ and leads to the following interpretations. Immediately after the end of the HU block (i.e. 5 hr after HU injection) the modal cell‐cycle transit time is reduced to 8 hr. By 17 hr after HU, the modal transit time is increased to 10 hr. Repopulation of the proliferating compartment, i.e. restoration of the proliferating compartment back to the control value, occurs between 12 and 17 hr after HU injection and probably consists of both recycling of the proliferating cells (i.e. they do not progress up into the non‐proliferating compartment) and recruitment of the non‐proliferating cells into active proliferation. Also, the rate at which the non‐proliferating cells move onto the villi is reduced temporarily. The overall recovery process results in a crypt which temporarily is larger than control and produces villi cells at a rate which is faster than the control. The time when the crypt size and villus cell production rate return to normal cannot be established using the available data.