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诱导型一氧化氮合酶和CD11bGr1细胞损害肿瘤引流淋巴管的淋巴收缩功能。

Inducible Nitric Oxide Synthase and CD11bGr1 Cells Impair Lymphatic Contraction of Tumor-Draining Lymphatic Vessels.

作者信息

Liao Shan, Bouta Echoe M, Morris Linda M, Jones Dennis, Jain Rakesh K, Padera Timothy P

机构信息

1 Edwin L. Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.

出版信息

Lymphat Res Biol. 2019 Jun;17(3):294-300. doi: 10.1089/lrb.2018.0013. Epub 2018 Oct 24.

Abstract

Metastatic tumor cells spread through lymphatic vessels and colonize draining lymph nodes (LNs). It is known that tumors induce lymphangiogenesis to enhance lymphatic metastasis and that metastatic cancer cells are carried by lymph flow to LNs. Here, we investigated the molecular and cellular regulation of collecting lymphatic vessel contraction in vessels draining a metastatic tumor using intravital microscopy. In tumor-draining collecting lymphatic vessels, we found vessel contraction was suppressed. The infiltration of peritumor tissue by inducible nitric oxide synthase positive and CD11bGr1 myeloid cells played a critical role in the suppression of lymphatic contraction. Depletion of Gr1 cells with an anti-Gr1 antibody improved contraction of tumor-draining lymphatic vessels. In addition, inducing tumor cell death restored lymphatic contraction in nude mice. These findings indicate that tumors contribute to regulation of lymphatic transport in a reversible manner, warranting further investigation into the role of impaired lymphatic transport in cancer progression.

摘要

转移性肿瘤细胞通过淋巴管扩散并在引流淋巴结(LN)中定植。已知肿瘤会诱导淋巴管生成以增强淋巴转移,并且转移性癌细胞会随淋巴液流向淋巴结。在此,我们使用活体显微镜研究了引流转移性肿瘤的淋巴管中集合淋巴管收缩的分子和细胞调控。在肿瘤引流的集合淋巴管中,我们发现血管收缩受到抑制。诱导型一氧化氮合酶阳性和CD11bGr1髓样细胞对肿瘤周围组织的浸润在抑制淋巴管收缩中起关键作用。用抗Gr1抗体清除Gr1细胞可改善肿瘤引流淋巴管的收缩。此外,诱导肿瘤细胞死亡可恢复裸鼠的淋巴管收缩。这些发现表明肿瘤以可逆的方式参与淋巴管运输的调节,这值得进一步研究淋巴管运输受损在癌症进展中的作用。

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