scholarly journals P3.01-050 Isolation and Characterization of Lymphatic Endothelial Cells from Neoplastic and Normal Human Lung

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.


2007 ◽  
Vol 21 (5) ◽  
Author(s):  
Hideki Ohta ◽  
Kenichi Katsube ◽  
Jyun‐ichi Ogawa ◽  
Masaki Yanagishita

1998 ◽  
Vol 46 (2) ◽  
pp. 165-176 ◽  
Author(s):  
Birthe Sauter ◽  
Dagmar Foedinger ◽  
Barbara Sterniczky ◽  
Klaus Wolff ◽  
Klemens Rappersberger

We performed a comparative investigation of the immunomorphological characteristics of lymphatic and blood microvascular endothelial cells in normal human skin, cutaneous lymphangiomas, and hemangiomas, employing a pre-embedding immunogold electron microscopic technique. We stained for cell membrane proteins that are commonly used for light microscopic characterization of blood endothelial cells. With blood microvascular endothelial cells, we observed uniform labeling of the luminal cell membranes with monoclonal antibodies (MAbs) JC70 (CD31), EN-4 (CD31), BMA120, PAL-E, and QBEND-10 (CD34), and strong staining of the vascular basal lamina for Type IV collagen under normal and pathological conditions. In contrast, lymphatic microvascular endothelial cells in normal human skin and in lymphangiomas displayed, in addition to a luminal labeling, pronounced expression of CD31 and CD34 along the abluminal cell membranes. Moreover, CD31 was preferentially detected within intercellular junctions. The expression of CD34 was mostly confined to abluminal endothelial microprocesses and was upregulated in lymphangiomas and hemangiomas. Type IV collagen partially formed the luminal lining of initial lymphatics and occasionally formed bridges over interendothelial gaps. Our findings suggest a function of transmigration protein CD31 in recruitment of dendritic cells into the lymphatic vasculature. CD34 labeling may indicate early endothelial cell sprouting. The distribution of Type IV collagen also supports its role as a signal for migration and tube formation for lymphatic endothelial cells.


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

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