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Inducible Nitric Oxide Synthase and CD11b+Gr1+ Cells Impair Lymphatic Contraction of Tumor-Draining Lymphatic Vessels
Resource type
Authors/contributors
- Liao, Shan (Author)
- Bouta, Echoe M. (Author)
- Morris, Linda M. (Author)
- Jones, Dennis (Author)
- Jain, Rakesh K. (Author)
- Padera, Timothy P. (Author)
Title
Inducible Nitric Oxide Synthase and CD11b+Gr1+ Cells Impair Lymphatic Contraction of Tumor-Draining Lymphatic Vessels
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.
Publication
Lymphatic Research and Biology
Volume
17
Issue
3
Pages
294-300
Date
2019-06
Journal Abbr
Lymphat Res Biol
Language
eng
ISSN
1557-8585
Library Catalog
PubMed
Lipedema Foundation Award
LF01
Citation
Liao, S., Bouta, E. M., Morris, L. M., Jones, D., Jain, R. K., & Padera, T. P. (2019). Inducible Nitric Oxide Synthase and CD11b+Gr1+ Cells Impair Lymphatic Contraction of Tumor-Draining Lymphatic Vessels. Lymphatic Research and Biology, 17(3), 294–300. https://doi.org/10.1089/lrb.2018.0013
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