Proto-oncogene expression during early myeloid differentiation of normal peripheral blood progenitor cells

Peripheral blood mononuclear cells cultured in liquid medium with fetal calf serum undergo differentiation to myeloblasts (7 days) and then mature granulocytes (14–21 days). This culture system was used to study proto-oncogene expression during pre-myeloblast myeloid differentiation. c- myc mRNA was...

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Veröffentlicht in:Leukemia research 1989, Vol.13 (2), p.165,171-169,172
Hauptverfasser: Baer, Maria R., Xue Zhi Gao, Sato, Hiroshi, Singh, Pradeep, Preisler, Harvey D.
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container_end_page 169,172
container_issue 2
container_start_page 165,171
container_title Leukemia research
container_volume 13
creator Baer, Maria R.
Xue Zhi Gao
Sato, Hiroshi
Singh, Pradeep
Preisler, Harvey D.
description Peripheral blood mononuclear cells cultured in liquid medium with fetal calf serum undergo differentiation to myeloblasts (7 days) and then mature granulocytes (14–21 days). This culture system was used to study proto-oncogene expression during pre-myeloblast myeloid differentiation. c- myc mRNA was present in the peripheral blood mononuclear cells placed into culture, fell during the first 2–4 days of culture and then rose between days 2–4 and day 7 of culture, prior to and coincident with the appearance of myeloblasts. Histone H3 mRNA was absent or present at very low levels at initiation of cultures, and then rose throughout the first 7 days of culture. c- fms mRNA was absent at initiation of cultures, and appeared on days 2–5 of culture, prior to the appearance of myeloblasts. c- fos mRNA was not detected during differentiation of peripheral blood mononuclear cells to myeloblasts. Elucidation of patterns of proto-oncogene expression during normal myeloid differentiation is a prerequisite for interpretation of proto-oncogene expression in myeloid leukemia cells.
doi_str_mv 10.1016/0145-2126(89)90141-0
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This culture system was used to study proto-oncogene expression during pre-myeloblast myeloid differentiation. c- myc mRNA was present in the peripheral blood mononuclear cells placed into culture, fell during the first 2–4 days of culture and then rose between days 2–4 and day 7 of culture, prior to and coincident with the appearance of myeloblasts. Histone H3 mRNA was absent or present at very low levels at initiation of cultures, and then rose throughout the first 7 days of culture. c- fms mRNA was absent at initiation of cultures, and appeared on days 2–5 of culture, prior to the appearance of myeloblasts. c- fos mRNA was not detected during differentiation of peripheral blood mononuclear cells to myeloblasts. 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subjects Biological and medical sciences
Blotting, Northern
Cell Differentiation
Cell differentiation, maturation, development, hematopoiesis
Cell physiology
Cells, Cultured
differentiation
Fundamental and applied biological sciences. Psychology
Granulocytes - physiology
Hematopoietic Stem Cells - physiology
Histones - metabolism
Humans
Molecular and cellular biology
myeloid progenitors
Proto-Oncogene Proteins - metabolism
Proto-Oncogene Proteins c-myc
Proto-Oncogenes
RNA, Messenger - metabolism
Transcription, Genetic
title Proto-oncogene expression during early myeloid differentiation of normal peripheral blood progenitor cells
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