Therapeutic differentiation and maturation of lymphatic vessels after lymph node dissection and tran

Author:  ["Tuomas Tammela","Anne Saaristo","Tanja Holopainen","Johannes Lyytikkä","Anna Kotronen","Miia Pitkonen","Usama Abo-Ramadan","Seppo Ylä-Herttuala","Tatiana V Petrova","Kari Alitalo"]

Publication:  Nature Medicine

CITE.CC academic search helps you expand the influence of your papers.

Tags:     Medicine

Abstract

Surgery or radiation therapy of metastatic cancer often damages lymph nodes, leading to secondary lymphedema. Here we show, using a newly established mouse model, that collecting lymphatic vessels can be regenerated and fused to lymph node transplants after lymph node removal. Treatment of lymph node–excised mice with adenovirally delivered vascular endothelial growth factor-C (VEGF-C) or VEGF-D induced robust growth of the lymphatic capillaries, which gradually underwent intrinsic remodeling, differentiation and maturation into functional collecting lymphatic vessels, including the formation of uniform endothelial cell-cell junctions and intraluminal valves. The vessels also reacquired pericyte contacts, which downregulated lymphatic capillary markers during vessel maturation. Growth factor therapy improved the outcome of lymph node transplantation, including functional reconstitution of the immunological barrier against tumor metastasis. These results show that growth factor–induced maturation of lymphatic vessels is possible in adult mice and provide a basis for future therapy of lymphedema.

Cite this article

Tammela, T., Saaristo, A., Holopainen, T. et al. Therapeutic differentiation and maturation of lymphatic vessels after lymph node dissection and transplantation. Nat Med 13, 1458–1466 (2007). https://doi.org/10.1038/nm1689

View full text

>> Full Text:   Therapeutic differentiation and maturation of lymphatic vessels after lymph node dissection and tran

In vivo gene silencing identifies the Mycobacterium tuberculosis proteasome as essential for the bac

PPAR-γ regulates osteoclastogenesis in mice