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Effects of Granulocyte Colony-Stimulating Factor on Proliferation and Apoptosis of B Cells in Bone Marrow of Healthy Donors.

Authors :
Zhai SZ
Guo HD
Li SQ
Zhao XS
Wang Y
Xu LP
Liu KY
Huang XJ
Chang YJ
Source :
Transplantation proceedings [Transplant Proc] 2020 Jan - Feb; Vol. 52 (1), pp. 345-352. Date of Electronic Publication: 2020 Jan 07.
Publication Year :
2020

Abstract

Background and Objective: The aim of this study was to investigate the effects of granulocyte colony-stimulating factor (G-CSF) on the proliferation and apoptosis of bone marrow (BM) B cells from healthy donors and its mechanism.<br />Materials and Methods: The proliferation ability and apoptosis of BM cells from healthy donors before and after in vivo G-CSF application were determined by multiparameter flow cytometry. The gene expression of B cells was detected by RNA-Seq. In vitro experiments were performed to investigate the effects of G-CSF on the proliferation and apoptosis of BM B cells through which gene.<br />Results: Treating healthy donors with G-CSF significantly decreased proliferation and increased apoptosis of BM B cells. The proliferation of CD19 <superscript>+</superscript> CD27 <superscript>-</superscript> B cell subgroup and CD19 <superscript>+</superscript> CD24 <superscript>hi</superscript> CD38 <superscript>hi</superscript> B cell subset were also decreased. G-CSF also significantly altered proapoptotic genes, cell cycle arrest genes, and DNA replication and cell cycle genes, especially significantly increased SOCS1 expression of BM B cells. In vitro experiments showed that SOCS1 overexpression did not affect B cell proliferation ability and apoptosis.<br />Conclusions: Our results suggest that extensive effects of G-CSF on BM B cells, such as inhibiting proliferation, inducing apoptosis, and altering a series of gene expression.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-2623
Volume :
52
Issue :
1
Database :
MEDLINE
Journal :
Transplantation proceedings
Publication Type :
Academic Journal
Accession number :
31918969
Full Text :
https://doi.org/10.1016/j.transproceed.2019.11.004