File | |
Title |
Down-regulation of c-myc protein expression in g0/g1 phase of the cell cycle during the induction of differentiation by 1,25 dihydroxyvitamin D3 in HL-60 cells
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Creator |
Ishikura Hiroto
Tsumura Hiroto
Sato Yukie
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Source Title |
Shimane journal of medical science
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Volume | 16 |
Issue | 2 |
Start Page | 45 |
End Page | 49 |
Journal Identifire |
ISSN 03865959
EISSN 24332410
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Descriptions |
It is well established that c-myc expression is down-regulated during induction of differentiation in various leukemia cell lines including HL-60 human myeloid leukemia cells. Previously we have shown that c-myc protein expression was specifically down-regulated in G0/G1 phase of the cell cycle during induction of granulocytic differentiation with dimetylsulfoxide (DMSO) in HL-60 cells. In the present study, we examined whether c-myc protein expression is also down-regulated in G0/G1 phase during monocytic differentiation of HL-60 cells. HL-60 cells can be induced to differentiate along monocytic lineage by treatment with 1,25 dihydroxyvitamin D3 (D3). C-myc protein expression was down-regulated after 72h of treatment with D3 in HL-60 cells. Simultaneous analysis of protein level and cell cycle using a two-color flow cytometry showed that the down-regulation of c-myc protein expression occurred specifically in G0/G1 phase. Down-regulation of c-myc protein expression in G0/G1 phase was more clearly shown by using synchronized cell population that was arrested at G0/G1 phase by serum starvation. Furthermore, G0/G1-synchronized cells showed a higher susceptibility to differentiation in response to D3. These results suggest that c-myc protein is down-regulated in G0/G1-specific phase during not only granulocytic differentiation but also monocytic differentiation, and down-regulation of c-myc protein expression in G0/G1 phase is involved in the program of differentiation of HL-60 cells.
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Subjects | |
Language |
eng
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Resource Type | departmental bulletin paper |
Publisher |
Shimane Medical University
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Date of Issued | 1998-12-01 |
Publish Type | Version of Record |
Access Rights | open access |
Relation |
[NCID] AA00841586
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