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Characterization of the early and late stages of myelomonocytic leukemia induced by friend helper‐independent virus F‐MuLV: Isolation and induction of friend myelomonocytic leukemic cell lines
Author(s) -
Shibuya Tsunefumi,
Mak Tak W.
Publication year - 1983
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041170302
Subject(s) - leukemia , acute myelomonocytic leukemia , biology , cell culture , progenitor cell , k562 cells , microbiology and biotechnology , haematopoiesis , murine leukemia virus , virus , immunology , virology , stem cell , genetics
With the use of cloned helper‐independent Friend leukemia virus (F‐MuLV), we have induced a high incidence (∼ 70%) of myelomonocytic leukemia in mice resistant ( Fv‐6 rr or Fv‐6 rs ) to erythroleukemia induction by this virus. The spleen cells from these mice (DBA/2 or BALB/c × DBA/2) were found to contain a high level of progenitor cells capable of forming granulocytic and macrophage colonies (CFU‐GM). These CFU‐GM, however, were different from those in the speens of uninfected mice, as they were either very sensitive to or independent of conditioned medium. No erythroid progenitor bursts (BFU‐E) or precursor (CFU‐E) cells were detected in the speens of these diseased animals. If these mice with myelomonocytic leukemia were kept alive by transfusion of red blood cells from uninfected mice, tumorigenic cell lines, capable of being transplanted, into adult mice can be isolated. Three such cell lines TTA‐1, TTA‐3, and TTA‐9 have been established, and they retain their morphology of monocytes and macrophages as well as being positive for the monocyte‐specific stain α‐naphtyl‐acetate esterase. These myelomonocytic leukemia cell lines can also be induced in culture by speen cell‐conditioned medium to differentiate into macrophages. Other conditioned media such as L‐cell‐conditioned medium, phytophemmaglutinin‐stimulated leukocyte‐conditioned medium, and WEHI‐3 conditioned medium were less effective in their abilities to stimulate differentiation in these myelomonocytic leukemia cell lines.