Inducible Nitric Oxide Synthase and CD11b+Gr1+ Cells Impair Lymphatic Contraction of Tumor-Draining Lymphatic Vessels

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

Abstract

Background: 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. Methods and Results: 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 CD11b+Gr1+ 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. Conclusions: 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.

Keywords: inducible nitric oxide synthase; lymph node metastasis; lymphatic contraction; lymphatic vessels; nitric oxide; tumor draining.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • CD11b Antigen / genetics
  • CD11b Antigen / metabolism*
  • Cell Line, Tumor
  • Disease Models, Animal
  • Heterografts
  • Lymph Nodes / pathology
  • Lymphatic Metastasis
  • Lymphatic Vessels / metabolism*
  • Lymphatic Vessels / physiopathology
  • Mice
  • Models, Biological
  • Neoplasms / etiology
  • Neoplasms / metabolism*
  • Neoplasms / pathology*
  • Neoplasms / physiopathology
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / metabolism*
  • Receptors, Chemokine / genetics
  • Receptors, Chemokine / metabolism*
  • Vasoconstriction* / genetics

Substances

  • Biomarkers
  • CD11b Antigen
  • Receptors, Chemokine
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse