Isolation and characterization of primary lymphatic endothelial cells from rat thoracic duct

2007 ◽  
Vol 21 (5) ◽  
Author(s):  
Hideki Ohta ◽  
Kenichi Katsube ◽  
Jyun‐ichi Ogawa ◽  
Masaki Yanagishita
2017 ◽  
Vol 12 (1) ◽  
pp. S1150
Author(s):  
Federico Quaini ◽  
Bruno Lorusso ◽  
Angela Falco ◽  
Denise Madeddu ◽  
Costanza Lagrasta ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-12 ◽  
Author(s):  
Bruno Lorusso ◽  
Angela Falco ◽  
Denise Madeddu ◽  
Caterina Frati ◽  
Stefano Cavalli ◽  
...  

Characterization of lymphatic endothelial cells from the respiratory system may be crucial to investigate the role of the lymphatic system in the normal and diseased lung. We describe a simple and inexpensive method to harvest, isolate, and expand lymphatic endothelial cells from the human lung (HL-LECs). Fifty-five samples of healthy lung selected from patients undergoing lobectomy were studied. A two-step purification tool, based on paramagnetic sorting with monoclonal antibodies to CD31 and Podoplanin, was employed to select a pure population of HL-LECs. The purity of HL-LECs was assessed by morphologic criteria, immunocytochemistry, flow cytometry, and functional assays. Interestingly, these cells retainin vitroseveral receptor tyrosine kinases (RTKs) implicated in cell survival and proliferation. HL-LECs represent a clinically relevant cellular substrate to study lymphatic biology, lymphoangiogenesis, interaction with microbial agents, wound healing, and anticancer therapy.


2000 ◽  
Vol 37 (1) ◽  
pp. 85-95 ◽  
Author(s):  
E Sinzelle ◽  
J P Duong Van Huyen ◽  
S Breiteneder-Geleff ◽  
E Braunberger ◽  
A Deloche ◽  
...  

2011 ◽  
Vol 356 (1) ◽  
pp. 171
Author(s):  
Ying Yang ◽  
Kimberle Shen ◽  
Sathish Srinivasan ◽  
Amira Masri ◽  
Joshua Scallan ◽  
...  

1980 ◽  
Vol 35 (2) ◽  
pp. 374-381 ◽  
Author(s):  
Stuart K. Williams ◽  
John F. Gillis ◽  
Maureen A. Matthews† ◽  
Roger C. Wagnert ◽  
Mark W. Bitensky

Blood ◽  
2010 ◽  
Vol 116 (17) ◽  
pp. 3356-3366 ◽  
Author(s):  
Karlien Hermans ◽  
Filip Claes ◽  
Wouter Vandevelde ◽  
Wei Zheng ◽  
Ilse Geudens ◽  
...  

Abstract The molecular basis of lymphangiogenesis remains incompletely characterized. Here, we document a novel role for the PDZ domain-containing scaffold protein synectin in lymphangiogenesis using genetic studies in zebrafish and tadpoles. In zebrafish, the thoracic duct arises from parachordal lymphangioblast cells, which in turn derive from secondary lymphangiogenic sprouts from the posterior cardinal vein. Morpholino knockdown of synectin in zebrafish impaired formation of the thoracic duct, due to selective defects in lymphangiogenic but not angiogenic sprouting. Synectin genetically interacted with Vegfr3 and neuropilin-2a in regulating lymphangiogenesis. Silencing of synectin in tadpoles caused lymphatic defects due to an underdevelopment and impaired migration of Prox-1+ lymphatic endothelial cells. Molecular analysis further revealed that synectin regulated Sox18-induced expression of Prox-1 and vascular endothelial growth factor C–induced migration of lymphatic endothelial cells in vitro. These findings reveal a novel role for synectin in lymphatic development.


Sign in / Sign up

Export Citation Format

Share Document