Fig. 1.
Fig. 1. (A) Kinetics of appearance after TM injection of peritoneal cells and of adherent peritoneal cells that enter S phase in response to CSF-1. At various times after intraperitoneal injection of TM, peritoneal cell numbers were counted (□; see the Materials and Methods). Data are the mean values ± SEM and are pooled from 5 experiments, each with 8 mice. Also, at various times after intraperitoneal injection of TM, adherent cells were treated in vitro for 4 days with CSF-1 and [3H]-TdR (•; see the Materials and Methods). Autoradiography was used to measure the number of S-phase cells (see the Materials and Methods). Data are the mean values ± SEM from triplicate cultures and are from a representative experiment that was repeated a total of 3 times. (B) Kinetics of appearance of peritoneal M-CFCs. At various times after intraperitoneal injection of TM, M-CFCs were measured as agar colonies (1,000 cells plated; see the Materials and Methods). Data are plotted as the number of M-CFCs in the peritoneal cavity (▵) using the total cell numbers presented in (A) and as a percentage of the peritoneal cells (•; mean values ± SEM from triplicate cultures) and are from a representative experiment that was repeated a total of 3 times. When error bars are not presented, the errors are smaller than the size of the symbol.

(A) Kinetics of appearance after TM injection of peritoneal cells and of adherent peritoneal cells that enter S phase in response to CSF-1. At various times after intraperitoneal injection of TM, peritoneal cell numbers were counted (□; see the Materials and Methods). Data are the mean values ± SEM and are pooled from 5 experiments, each with 8 mice. Also, at various times after intraperitoneal injection of TM, adherent cells were treated in vitro for 4 days with CSF-1 and [3H]-TdR (•; see the Materials and Methods). Autoradiography was used to measure the number of S-phase cells (see the Materials and Methods). Data are the mean values ± SEM from triplicate cultures and are from a representative experiment that was repeated a total of 3 times. (B) Kinetics of appearance of peritoneal M-CFCs. At various times after intraperitoneal injection of TM, M-CFCs were measured as agar colonies (1,000 cells plated; see the Materials and Methods). Data are plotted as the number of M-CFCs in the peritoneal cavity (▵) using the total cell numbers presented in (A) and as a percentage of the peritoneal cells (•; mean values ± SEM from triplicate cultures) and are from a representative experiment that was repeated a total of 3 times. When error bars are not presented, the errors are smaller than the size of the symbol.

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