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可溶性因子和三维培养在肠道巨噬细胞体外分化中的作用

Role of soluble factors and three-dimensional culture in in vitro differentiation of intestinal macrophages.

作者信息

Spoettl Tanja, Hausmann Martin, Menzel Katrin, Piberger Heidi, Herfarth Hans, Schoelmerich Juergen, Bataille Frauke, Rogler Gerhard

机构信息

Department of Internal Medicine I, University of Regensburg, Regensburg 93042, Germany.

出版信息

World J Gastroenterol. 2007 Feb 21;13(7):1032-41. doi: 10.3748/wjg.v13.i7.1032.

Abstract

AIM

To examine the factor(s) involved in differentiation of intestinal macrophages (IMACs) using a recently established in vitro model.

METHODS

To test whether soluble or membrane bound factors induce IMAC-differentiation, freshly elutriated monocytes (MO) were incubated with conditioned media or cell membranes of intestinal epithelial cells (IEC) or cultured with IEC in transwell systems. To determine the importance of an active migration of MO, three-dimensional aggregates from a 1:1-mixture of MO and IEC were examined by immunohistochemistry and flow cytometry. Apoptosis was examined by caspase-3 Western blots. Extracellular matrix production in differentiation models was compared by immunohistochemistry.

RESULTS

IMAC differentiation was observed in a complex three-dimensional co-culture model (multicellular spheroid, MCS) with IEC after migration of MO into the spheroids. By co-culture of MO with conditioned media or membrane preparations of IEC no IMAC differentiation was induced. Co-culture of MO with IEC in transwell-cultures, with the two cell populations separated by a membrane also did not result in intestinal-like differentiation of MO. In contrast to IEC-spheroids with immigrating MO in mixed MCS of IEC and MO only a small subpopulation of MO was able to survive the seven day culture period.

CONCLUSION

Intestinal-like differentiation of MO in vitro is only induced in the complex three-dimensional MCS model after immigration of MO indicating a role of cell-matrix and/or cell-cell interactions during the differentiation of IMACs.

摘要

目的

利用最近建立的体外模型研究参与肠道巨噬细胞(IMACs)分化的因素。

方法

为了测试可溶性或膜结合因子是否诱导IMAC分化,将新鲜淘洗的单核细胞(MO)与肠道上皮细胞(IEC)的条件培养基或细胞膜一起孵育,或在transwell系统中与IEC共培养。为了确定MO主动迁移的重要性,通过免疫组织化学和流式细胞术检查了MO和IEC 1:1混合物形成的三维聚集体。通过caspase-3免疫印迹检测细胞凋亡。通过免疫组织化学比较分化模型中的细胞外基质产生情况。

结果

在MO迁移到球体后,在与IEC的复杂三维共培养模型(多细胞球体,MCS)中观察到IMAC分化。MO与IEC的条件培养基或膜制剂共培养未诱导IMAC分化。MO与IEC在transwell培养中,两个细胞群体被膜隔开,也未导致MO向肠道样分化。与IEC球体中MO迁移的情况相反,在IEC和MO的混合MCS中,只有一小部分MO能够在7天的培养期内存活。

结论

MO在体外向肠道样分化仅在MO迁移后的复杂三维MCS模型中诱导,表明细胞-基质和/或细胞-细胞相互作用在IMACs分化过程中起作用。

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