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通过蛋白质芯片分析人类早孕蜕膜中的趋化因子、细胞因子和生长因子。

Profiling chemokines, cytokines and growth factors in human early pregnancy decidua by protein array.

作者信息

Engert Sabine, Rieger Lorenz, Kapp Michaela, Becker Jürgen C, Dietl Johannes, Kämmerer Ulrike

机构信息

Department of Obstetrics and Gynaecology, University of Wurzburg, Wurzburg, Germany.

出版信息

Am J Reprod Immunol. 2007 Aug;58(2):129-37. doi: 10.1111/j.1600-0897.2007.00498.x.

Abstract

PROBLEM

In human decidua, a significant increase of leukocytes including CD56(++)CD16(-) uterine natural killer (uNK) cells and CD14(+) monocytes has been observed with the onset of pregnancy. The mechanisms required for the recruitment of those cells to the uterus are still under debate. Cytokines and chemokines have been suggested as key factors for the regulation of these complex cellular migration and interaction processes.

METHOD OF STUDY

Investigation of the expression patterns of cytokines, chemokines and growth factors in human decidual tissue (7-8 weeks of gestation) was performed by protein array analysis. Isolated decidual leukocytes, i.e. CD56(++)CD16(-) uNK, CD14(+) monocytes as well as cytotrophoblast (CTB) and stromal cells were tested separately.

RESULTS

This analysis revealed the production of monocyte attracting chemokines (GRO, MCP-1), angiogenetic substances (EGF, VEGF, Angiogenin) as well as granulocyte activating peptides (ENA-78, IL-1beta, RANTES, IL-8) by decidual tissue and its cell subsets.

CONCLUSION

The observed pattern supports the role of decidua as a tissue which promotes angiogenesis, attracts monocytes and modulates the function of the latter.

摘要

问题

在人类蜕膜中,随着妊娠开始,已观察到包括CD56(++)CD16(-)子宫自然杀伤(uNK)细胞和CD14(+)单核细胞在内的白细胞显著增加。这些细胞募集至子宫所需的机制仍存在争议。细胞因子和趋化因子被认为是调节这些复杂细胞迁移和相互作用过程的关键因素。

研究方法

通过蛋白质阵列分析对人类蜕膜组织(妊娠7 - 8周)中细胞因子、趋化因子和生长因子的表达模式进行研究。分别对分离出的蜕膜白细胞,即CD56(++)CD16(-) uNK细胞、CD14(+)单核细胞以及细胞滋养层(CTB)细胞和基质细胞进行检测。

结果

该分析揭示了蜕膜组织及其细胞亚群可产生单核细胞吸引趋化因子(生长调节致癌基因蛋白、单核细胞趋化蛋白-1)、血管生成物质(表皮生长因子、血管内皮生长因子、血管生成素)以及粒细胞激活肽(ENA - 78、白细胞介素-1β、调节激活正常T细胞表达和分泌因子、白细胞介素-8)。

结论

观察到的模式支持蜕膜作为一种促进血管生成、吸引单核细胞并调节后者功能的组织所起的作用。

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