| Autor: |
Grinev VV; a Belarusian State University , F. Skoriny Avenue-4, 220050 Minsk , Belarus., Grigorovich SA; b Hematology and Blood Transfusion Research Institute , 160 Dolginovski Trakt, 223059 Minsk , Belarus., Shman TV; c Belarussian Center for Pediatric Oncology and Hematology, P.O Lesnoye-2, Minsk District , 223052 Belarus., Sheleg SV; b Hematology and Blood Transfusion Research Institute , 160 Dolginovski Trakt, 223059 Minsk , Belarus., Smolnikova VV; b Hematology and Blood Transfusion Research Institute , 160 Dolginovski Trakt, 223059 Minsk , Belarus., Potapnev MP; c Belarussian Center for Pediatric Oncology and Hematology, P.O Lesnoye-2, Minsk District , 223052 Belarus., Svirnovski AI; b Hematology and Blood Transfusion Research Institute , 160 Dolginovski Trakt, 223059 Minsk , Belarus. |
| Abstrakt: |
Two models of in vitro induction of human IM-9 lymphoblastoid cell line resistance to LAK cell-mediated killing were compared. IM-9 cell line variants were selected in vitro by prolonged exposure to LAK cells or to etoposide. Sensitivity to killing by LAK cells or by etoposide, conjugation with LAK cells and surface marker patterns were compared. Both LAK-cell-selected cell subline (IM-9/SL-15) and etoposide-selected cell subline (IM-9/ER) have acquired resistance to LAK cell-mediated death. IM-9/ER cells, but not IM-9/SL-15 cells, were 3.2-fold less sensitive to etoposide as compared to parental IM-9 cells. IM-9/SL-15 cells revealed decreased conjugation with LAK cells and augmented CDlla/CD18 surface molecule expression as compared to IM-9 line. In contrast, IM-9/ER cells displayed a level of conjugation with LAK cells equal to IM-9 cells, but loss of CD11a/C18 expression. Our results suggest different mechanisms of acquired resistance to LAK cells are operative in etoposide- or LAK-selected sublines, involving deterioration of LFA-1 molecule expression and altered conjugation properties, respectively. |
