scholarly journals Individual cell motion in healthy human skin microvasculature by reflectance confocal video microscopy

2020 ◽  
Vol 27 (6) ◽  
Author(s):  
Inga Saknite ◽  
Zijun Zhao ◽  
J. Randall Patrinely ◽  
Michael Byrne ◽  
Madan Jagasia ◽  
...  
2020 ◽  
Vol 83 (6) ◽  
pp. AB217
Author(s):  
Inga Saknite ◽  
Zijun Zhao ◽  
J. Randall Patrinely ◽  
Michael Byrne ◽  
Madan Jagasia ◽  
...  

Physiology ◽  
2001 ◽  
Vol 16 (1) ◽  
pp. 33-37 ◽  
Author(s):  
M. Schmelz ◽  
L. J. Petersen

The combination of vasodilation and protein extravasation following activation of nociceptors has been termed “neurogenic inflammation.” In contrast to rodents, no neurogenic protein extravasation can be elicited in healthy human skin. Dermal microdialysis has considerably increased our knowledge about neurogenic inflammation in human skin, including the involvement of mast cells.


2005 ◽  
Vol 6 (1) ◽  
pp. 21-31 ◽  
Author(s):  
Michael Wurzel ◽  
Carlo Schaller ◽  
Matthias Simon ◽  
Andreas Deutsch

The malignant brain tumourGlioblastoma multiforme(GBM) displays a highly invasive behaviour. Spreading of the malignant cells appears to be guided by the white matter fibre tracts within the brain. In order to understand the global growth process we introduce a lattice-gas cellular automaton model which describes the local interaction between individual malignant cells and their neighbourhood. We consider interactions between cells (brain cells and tumour cells) and between malignant cells and the fibre tracts in the brain, which are considered as a prepattern. The prepattern implies persistent individual cell motion along the fibre structure. Simulations with the model show that only the inclusion of the prepattern results in invading tumour and growing tumour islets in front of the expanding tumour bulk (i.e. the growth pattern observed in clinical practice). Our results imply that the infiltrative growth of GBMs is, in part, determined by the physical structure of the surrounding brain rather than by intrinsic properties of the tumour cells.


2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Richard S. Ahn ◽  
Keyon Taravati ◽  
Kevin Lai ◽  
Kristina M. Lee ◽  
Joanne Nititham ◽  
...  

2013 ◽  
Vol 1 (4) ◽  
Author(s):  
R. Srivastav ◽  
A. Singh ◽  
P. K. Jangir ◽  
C. Kumari ◽  
S. Muduli ◽  
...  

2019 ◽  
Vol 139 (9) ◽  
pp. S256
Author(s):  
O. Somogyi ◽  
B. Medgyesi ◽  
A. Jenei ◽  
Z. Dajnoki ◽  
K. Gáspár ◽  
...  
Keyword(s):  

2018 ◽  
Vol 98 (2) ◽  
pp. 256-261 ◽  
Author(s):  
M Brandwein ◽  
G Fuks ◽  
A Israel ◽  
A Al-Ashhab ◽  
D Nejman ◽  
...  

2007 ◽  
Vol 85 (5) ◽  
pp. 363-369 ◽  
Author(s):  
Catherine E Angel ◽  
Elizabeth George ◽  
Lena L Ostrovsky ◽  
P Rod Dunbar

2016 ◽  
Vol 6 (2) ◽  
pp. 64-69
Author(s):  
J. Wosek ◽  
I. Radziejewska ◽  
E. Andrulewicz

Purpose: The membrane-anchored MUC1 mucin is typically expressed on normal and cancerous epithelial cells. Non-epithelial localization of this mucin is rare. However, the presence of MUC1 in human skin fibroblasts has been recently unexpectedly revealed. The aim of the study was to prove the expression of MUC1 mucin in human skin fibroblasts and the examine of the influence of luteolin on its expression. Materials and methods: ELISA tests and real-time PCR analysis were used to assess the expression of MUC1 mucin in fibroblast cells cocultured with 30 μM concentration of luteolin. Results: The expression of MUC1 was revealed in human skin fibroblasts. Luteolin decreased the relative level of mucin in cell lysates and media. Statistically significant decreased expression of MUC1 gene after luteolin treatment of fibroblasts cells was also revealed. Conclusion: Our results prove non-epithelial localization of MUC1 mucin. Luteolin inhibits the expression of MUC1 mucin in healthy human skin fibroblasts.


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