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巨核细胞诱导的成纤维细胞增殖通过IL-6/IL-3共刺激得以增强,且依赖于分泌和黏附事件。

Megakaryocyte induced fibroblast proliferation is enhanced by costimulation with IL-6/IL-3 and dependent on secretory and adhesion events.

作者信息

Schmitz B, Wickenhauser C, Thiele J, Frimpong S, Brockbals C, Selbach B, Mueller C, Fischer R

机构信息

Institute of Pathology, University of Cologne, Germany.

出版信息

Leuk Res. 1999 Aug;23(8):723-9. doi: 10.1016/s0145-2126(99)00091-0.

Abstract

Experimental data are in keeping with the finding that megakaryocytes isolated from normal human bone marrow may promote fibroblast growth. This effect can be significantly enhanced by interleukin (IL)-3. In this context it has been demonstrated that IL-3 induces the release of platelet-derived growth factor (PDGF) and transforming growth factor beta1 (TGFbeta1) from megakaryocytes, factors known to enhance fibroblast proliferation. The present in vitro study was performed to elucidate the action of several other cytokines which are able to influence the different steps of megakaryocyte maturation and function like stem cell factor (SCF), IL-6, and leukemia inhibitory factor (LIF) as well. Following an appropriate experimental design we were able to show that none of the mentioned cytokines enhanced megakaryocyte dependent fibroblast proliferation in the coculture assays. On the other hand, IL-6 in combination with IL-3 surpassed the IL-3 dependent action significantly. However, the combined IL-3/IL-6 effect was not explainable by an increased PDGF/TGF-beta secretion of the megakaryocytes. In transwell experiments the inhibition of cell-to-cell contact via tissue culture inserts generated a conspicuous impairment of fibroblast growth in the IL-3/IL-6 treated cocultures. This reversal surpassed even the effect on the untreated and IL-3 stimulated cocultures. Hence, a direct contact of both cell types probably inducing adhesion phenomenons and warranting a certain threshold of local PDGF/TGF-beta concentration is a prerequisite for the proliferative effect on fibroblasts in the costimulation experiments. These results are of special interest regarding the evolution of myelofibrosis in chronic myeloproliferative disorders (CMPDs) because (1) various progenitor cells including the megakaryocytic lineage are hypersensitive towards IL-3 and (2) an abnormal secretion of IL-6 is described for megakaryocytes in these disorders.

摘要

实验数据与以下发现相符

从正常人骨髓中分离出的巨核细胞可促进成纤维细胞生长。白细胞介素(IL)-3可显著增强这种作用。在这种情况下,已证明IL-3可诱导巨核细胞释放血小板衍生生长因子(PDGF)和转化生长因子β1(TGFβ1),这些因子已知可增强成纤维细胞增殖。进行本体外研究以阐明其他几种细胞因子的作用,这些细胞因子也能够影响巨核细胞成熟和功能的不同步骤,如干细胞因子(SCF)、IL-6和白血病抑制因子(LIF)。按照适当的实验设计,我们能够证明在共培养试验中,上述细胞因子均未增强巨核细胞依赖性成纤维细胞增殖。另一方面,IL-6与IL-3联合使用时,其作用明显超过单独使用IL-3的效果。然而,巨核细胞PDGF/TGF-β分泌增加并不能解释IL-3/IL-6的联合作用。在transwell实验中,通过组织培养插入物抑制细胞间接触,导致IL-3/IL-6处理的共培养物中成纤维细胞生长明显受损。这种逆转甚至超过了对未处理和IL-3刺激的共培养物的影响。因此,在共刺激实验中,两种细胞类型的直接接触可能诱导黏附现象并保证局部PDGF/TGF-β浓度达到一定阈值,这是对成纤维细胞产生增殖作用的前提条件。这些结果对于慢性骨髓增殖性疾病(CMPD)中骨髓纤维化的演变具有特殊意义,因为(1)包括巨核细胞系在内的各种祖细胞对IL-3高度敏感,(2)在这些疾病中,巨核细胞存在IL-6异常分泌的情况。

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