Autocrine Inhibition of Differentiation in HL-60 Cells by Secreted Proteinase 3

Various molecules have been reported to be involved in the induction of HL-60 cell differentiation by all-trans retinoic acid (ATRA). Notably, the transfection of an antisense oligonucleotide targeting proteinase 3 (PRTN3, formerly known as myeloblastin) into HL-60 cells induces differentiation, though the underlying mechanism remains unclear. Here we found that the levels of secreted PRTN3 were significantly reduced when differentiation was initiated by ATRA treatment, suggesting that secreted PRTN3 inhibits HL-60 cell differentiation. The addition of anti-PRTN3 antibody to the culture medium of HL-60 cells promoted their differentiation. Conversely, when ATRA-treated HL-60 cells were cultured in conditioned media prepared from HEK293 cells transfected with the preproPRTN3 plasmid, differentiation was significantly suppressed. Moreover, conditioned media from HEK293 cells transfected with an inactive PRTN3 mutant (S203G) also suppressed HL-60 cell differentiation. These results suggest that PRTN3 secreted from HL-60 cells has an autocrine inhibitory effect on differentiation, independent of its enzymatic activity.

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Journal
BPB Reports
Published
2025-01-01
DOI
https://doi.org/10.1248/bpbreports.8.3_80
Primary Topic
Signaling Pathways in Disease
Type
article
Field-Weighted Citation Impact
0.00

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article

Autocrine Inhibition of Differentiation in HL-60 Cells by Secreted Proteinase 3

Hitomi Fujishiro, Daigo Sumi, Robert Nakayama
BPB Reports
Signaling Pathways in Disease
article

Autocrine Inhibition of Differentiation in HL-60 Cells by Secreted Proteinase 3

Hitomi Fujishiro, Daigo Sumi, Robert Nakayama
article en

Abstract

Various molecules have been reported to be involved in the induction of HL-60 cell differentiation by all-trans retinoic acid (ATRA). Notably, the transfection of an antisense oligonucleotide targeting proteinase 3 (PRTN3, formerly known as myeloblastin) into HL-60 cells induces differentiation, though the underlying mechanism remains unclear. Here we found that the levels of secreted PRTN3 were significantly reduced when differentiation was initiated by ATRA treatment, suggesting that secreted PRTN3 inhibits HL-60 cell differentiation. The addition of anti-PRTN3 antibody to the culture medium of HL-60 cells promoted their differentiation. Conversely, when ATRA-treated HL-60 cells were cultured in conditioned media prepared from HEK293 cells transfected with the preproPRTN3 plasmid, differentiation was significantly suppressed. Moreover, conditioned media from HEK293 cells transfected with an inactive PRTN3 mutant (S203G) also suppressed HL-60 cell differentiation. These results suggest that PRTN3 secreted from HL-60 cells has an autocrine inhibitory effect on differentiation, independent of its enzymatic activity.

BPB ReportsVol. 8(3)
Tokushima Bunri University (JP)
Ministry of Education, Culture, Sports, Science and Technology
Zero hunger
Openalex Percentile: Top 90%
Signaling Pathways in Disease
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