Cationic liposomes enhance targeted delivery and expression of exogenous DNA mediated by N-terminal modified poly(l-lysine)-antibody conjugate in mouse lung endothelial cells

Author(s):  
Vladimir S. Trubetskoy ◽  
Vladimir P. Torchilin ◽  
Stephen Kennel ◽  
Leaf Huang
2005 ◽  
Vol 12 (3) ◽  
pp. 510-518 ◽  
Author(s):  
Annette Wilson ◽  
Wen Zhou ◽  
Hunter C. Champion ◽  
Sean Alber ◽  
Zhi-Lue Tang ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Jinping Wang ◽  
Niu Niu ◽  
Suowen Xu ◽  
Zheng Gen Jin

2004 ◽  
Vol 13 (3) ◽  
pp. 150
Author(s):  
Jane Rose ◽  
Scott Wray ◽  
Hong Huang ◽  
Rostislav Likhotvorik ◽  
Dale Hoyt

2018 ◽  
Vol 9 ◽  
Author(s):  
Peter Wohlrab ◽  
Lourdes Soto-Gonzales ◽  
Thomas Benesch ◽  
Max Paul Winter ◽  
Irene Marthe Lang ◽  
...  

Blood ◽  
2011 ◽  
Vol 118 (2) ◽  
pp. 464-472 ◽  
Author(s):  
Yoshito Takeda ◽  
Qinglin Li ◽  
Alexander R. Kazarov ◽  
Mathieu Epardaud ◽  
Kutlu Elpek ◽  
...  

Abstract Tetraspanin protein CD151 on tumor cells supports invasion and metastasis. In the present study, we show that host animal CD151 also plays a critical role. CD151-null mice showed markedly diminished experimental lung metastasis after injection of Lewis lung carcinoma or B16F10 melanoma cells. Diminished tumor cell residence in the lungs was evident 6-24 hours after injection. Consistent with an endothelial cell deficiency, isolated CD151-null mouse lung endothelial cells showed diminished support for B16F10 adhesion and transendothelial migration, diminished B16F10-induced permeability, and diminished B16F10 adhesion to extracellular matrix deposited by CD151-null mouse lung endothelial cells. However, CD151 deletion did not affect the size of metastatic foci or subcutaneous primary B16F10 tumors, tumor aggregation, tumor clearance from the blood, or tumor-induced immune cell activation and recruitment. Therefore, the effects of host CD151 on metastasis do not involve altered local tumor growth or immune surveillance. VEGF-induced endothelial cell signaling through Src and Akt was diminished in CD151-null endothelial cells. However, deficient signaling was not accompanied by reduced endothelial permeability either in vitro (monolayer permeability assay) or in vivo (VEGF-stimulated Miles assay). In summary, diminished metastasis in CD151-null host animals may be due to impaired tumor-endothelial interactions, with underlying defects in mouse lung endothelial cell extracellular matrix production.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 5569-5569
Author(s):  
Ronny Kalash ◽  
Jeremiah Au ◽  
Michael W. Epperly ◽  
Julie P. Goff ◽  
Tracy M. Dixon ◽  
...  

Abstract Irradiation of the C57BL/6NHsd mouse lung results in pulmonary fibrosis. An acute phase (days 1 to 28) following irradiation recognized by an inflammatory response is followed by a latent phase (day 28 to day 125) where lung appears normal. Fibrosis occurs from day 125 till death characterized by bone marrow stromal cell migration to and proliferation in lung and increased collagen deposition. To investigate the role of endothelial cells, C57BL/6NHsd female mice were irradiated to 20 Gy to the pulmonary cavity shielding the rest of the body. Lung was excised at serial times, endothelial cells separated and tested for expression of endothelial genes vWF, VEGF, FGF1, CCL13 and CTGF; inflammatory genes IL-6; IGFbp7 and genes associated with fibrosis including MnSOD, Nrf2, NfkB, TLR4 and TGF-B. Endothelial cells were separated by using antibodies to CD45, or PECAM and sorting using flow cytometry. RNA was extracted using Triazol and gene expression determined using Real Time Polymerase Chain Reaction (RT-PCR). In irradiated total lung there was significant increase in endothelial cell markers at all times, compared to nonirradiated lung. Transcripts for vWF increased by 474.1 ± 388.5% (p = 0.017) by 2 days after irradiation, 520 ± 55.4% (p < 0.0001) at day 50, and 484.8 ± 26.8% (p < 0.0001) by day 200. VEGF and CTGF also remained elevated. In contrast, total lung MnSOD gene expression increased by 140.6 ± 46.1% at day 2 (p = 0.0185), decreased at day 50 to 17.9 ± 11.2% (p = 0.2808), and increased to 31.5 ± 11.4% by day 200 (p = 0.023). However, purified endothelial cells compared to alveolar cells, showed increased expression of not only the endothelial cell genes but also MnSOD, Nrf2, NfkB, and TGF-B. MnSOD expression in endothelial compared to alveolar cells at day 28 after irradiation was higher at 244.5 ± 7.8 vs 80.5 ± 4.9 (p = 0.0016), at day 150 expression was 140.1 ± 25.0 vs 5.4 ± 1.2 (p < 0.0001) and day 200 expression was 368.5 ± 6.4 vs 51.8 ± 10.3 (p = 0.0007). Lung endothelial cells display critical biomarkers of irradiation injury leading to fibrosis. Disclosures: No relevant conflicts of interest to declare.


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