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肾上腺髓质素可诱导淋巴管生成并改善继发性淋巴水肿。

Adrenomedullin induces lymphangiogenesis and ameliorates secondary lymphoedema.

作者信息

Jin Donghao, Harada Kazuhiko, Ohnishi Shunsuke, Yamahara Kenich, Kangawa Kenji, Nagaya Noritoshi

机构信息

Department of Regenerative Medicine and Tissue Engineering, National Cardiovascular Center Research Institute, 5-7-1 Fujishirodai, Suita, Osaka 565-8565, Japan.

出版信息

Cardiovasc Res. 2008 Dec 1;80(3):339-45. doi: 10.1093/cvr/cvn228. Epub 2008 Aug 16.

Abstract

AIMS

Adrenomedullin (AM) is a multifunctional peptide hormone that plays a significant role in vasodilation and angiogenesis. Lymphoedema is a common but refractory disorder that is difficult to be treated with conventional therapy. We therefore investigated whether AM promotes lymphangiogenesis and improves lymphoedema.

METHODS AND RESULTS

The effects of AM on lymphatic endothelial cells (LEC) were investigated. AM promoted proliferation, migration, and network formation of cultured human lymphatic microvascular endothelial cells (HLMVEC). AM increased intracellular cyclic adenosine monophosphate (cAMP) level in HLMVEC. The cell proliferation induced by AM was inhibited by a cAMP antagonist and mitogen-activated protein kinase kinase (MEK) inhibitors. Phosphorylated extracellular signal-regulated kinase (ERK) in HLMVEC was increased by AM. Continuous administration of AM (0.05 microg/kg/min) to BALB/c mice with tail lymphoedema resulted in a decrease in lymphoedema thickness. AM treatment increased the number of lymphatic vessels and blood vessels in the injury site.

CONCLUSION

AM promoted LEC proliferation at least in part through the cAMP/MEK/ERK pathway, and infusion of AM induced lymphangiogenesis and improved lymphoedema in mice.

摘要

目的

肾上腺髓质素(AM)是一种多功能肽类激素,在血管舒张和血管生成中发挥重要作用。淋巴水肿是一种常见但难治的疾病,难以用传统疗法治疗。因此,我们研究了AM是否促进淋巴管生成并改善淋巴水肿。

方法与结果

研究了AM对淋巴管内皮细胞(LEC)的影响。AM促进培养的人淋巴管微血管内皮细胞(HLMVEC)的增殖、迁移和网络形成。AM增加了HLMVEC细胞内的环磷酸腺苷(cAMP)水平。AM诱导的细胞增殖被cAMP拮抗剂和丝裂原活化蛋白激酶激酶(MEK)抑制剂抑制。AM增加了HLMVEC中磷酸化的细胞外信号调节激酶(ERK)。对患有尾部淋巴水肿的BALB/c小鼠持续给予AM(0.05微克/千克/分钟)导致淋巴水肿厚度降低。AM治疗增加了损伤部位淋巴管和血管的数量。

结论

AM至少部分通过cAMP/MEK/ERK途径促进LEC增殖,输注AM可诱导小鼠淋巴管生成并改善淋巴水肿。

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