Transferrin, derived from an OKT8-positive subpopulation of T lymphocytes, suppresses the production of granulocyte-macrophage colony- stimulatory factors from mitogen-activated T lymphocytes
Transferrin, derived from an OKT8-positive subpopulation of T lymphocytes, suppresses the production of granulocyte-macrophage colony- stimulatory factors from mitogen-activated T lymphocytes
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转铁蛋白源自 OKT8 阳性 T 淋巴细胞亚群,可抑制有丝分裂原激活的 T 淋巴细胞产生粒细胞-巨噬细胞集落刺激因子
DOI:
10.1182/blood.v62.1.37.bloodjournal62137
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发表时间:
1983
期刊:
影响因子:
20.3
通讯作者:
J. Bognacki
中科院分区:
文献类型:
--
作者:
H. Broxmeyer;Lien Lu;J. Bognacki
Purified human transferrin, when saturated with iron or zinc, decreased the production of granulocyte-macrophage colony-stimulating factors (GM- CSF) by human T lymphocytes that had been stimulated by phytohemagglutin or concanavalin-A. The iron-saturated transferrin was more active than the zinc-saturated transferrin. This effect was not seen for copper-saturated transferrin or for apotransferrin, and the inhibitory effect was seen whether production of GM-CSF occurred in the absence or presence of serum. If the lymphocytes were pretreated with monoclonal antibody against transferrin receptors, no suppressive effect with transferrin was seen. Transferrin did not have a direct effect on the granulocyte-macrophage colony or cluster-forming cells (CFU-GM) or on preformed GM-CSF. Transferrin-inhibitory activity was produced and released only from a subpopulation of T lymphocytes that had the OKT8+ antigenic phenotype. Release of this activity from OKT8+ lymphocytes, into culture medium at 37 degrees C, was first detected after 6–17 hr, but the capacity of the GM-CSF-producing lymphocytes to respond to transferrin-inhibitory activity was apparent only within the first 3 hr of placing the lymphocytes at 37 degrees C. These studies demonstrate feedback interactions confined to cells of the T-lymphocyte lineage that may be of relevance to the regulation of myelopoiesis.
DOI:
10.1172/jci110649
发表时间:
1982-09
期刊:
The Journal of clinical investigation
影响因子:
--
作者:
L. Pelus
通讯作者:
L. Pelus
影响因子:
20.3
作者:
Lebman,D;Trucco,M;Bottero,L;Lange,B;Pessano,S;Rovera,G
通讯作者:
Rovera,G
DOI:
--
发表时间:
1981
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Beller,DI;Unanue,ER
通讯作者:
Unanue,ER