TY - JOUR
T1 - Mechanical Stress Downregulates MHC Class I Expression on Human Cancer Cell Membrane
AU - La Rocca, Rosanna
AU - Tallerico, Rossana
AU - Hassan, Almosawy Talib
AU - Das, Gobind
AU - Tadepally, Lakshmikanth
AU - Matteucci, Marco
AU - Liberale, Carlo
AU - Mesuraca, Maria
AU - Scumaci, Domenica
AU - Gentile, Francesco
AU - Cojoc, Gheorghe
AU - Perozziello, Gerardo
AU - Ammendolia, Antonio
AU - Gallo, Adriana
AU - Kärre, Klas
AU - Cuda, Giovanni
AU - Candeloro, Patrizio
AU - Di Fabrizio, Enzo
AU - Carbone, Ennio
N1 - ©2014 La Rocca et al. This is an open-access article distributed under the terms of
the Creative Commons Attribution License
PY - 2014
Y1 - 2014
N2 - In our body, cells are continuously exposed to physical forces that can regulate
different cell functions such as cell proliferation, differentiation and death. In this work, we employed two different strategies to mechanically stress cancer cells. The cancer and healthy cell populations were treated either with mechanical stress delivered by a micropump (fabricated by deep X-ray nanolithography) or by ultrasound wave stimuli. A specific down-regulation of Major Histocompatibility Complex (MHC) class I molecules expression on cancer cell membrane compared to different kinds of healthy cells (fibroblasts, macrophages, dendritic and lymphocyte cells) was observed, stimulating the cells with forces in the range of nano-newton, and pressures between 1 and 10 bar (1 bar5100.000 Pascal), depending on the devices used. Moreover, Raman spectroscopy analysis, after mechanical treatment, in the range between 700–1800 cm-1, indicated a relative concentration variation of MHC class I. PCA analysis was also performed to distinguish control and stressed cells within different cell lines. These mechanical induced phenotypic changes increase the tumor immunogenicity, as revealed by the related increased susceptibility to Natural Killer (NK) cells cytotoxic recognition.
AB - In our body, cells are continuously exposed to physical forces that can regulate
different cell functions such as cell proliferation, differentiation and death. In this work, we employed two different strategies to mechanically stress cancer cells. The cancer and healthy cell populations were treated either with mechanical stress delivered by a micropump (fabricated by deep X-ray nanolithography) or by ultrasound wave stimuli. A specific down-regulation of Major Histocompatibility Complex (MHC) class I molecules expression on cancer cell membrane compared to different kinds of healthy cells (fibroblasts, macrophages, dendritic and lymphocyte cells) was observed, stimulating the cells with forces in the range of nano-newton, and pressures between 1 and 10 bar (1 bar5100.000 Pascal), depending on the devices used. Moreover, Raman spectroscopy analysis, after mechanical treatment, in the range between 700–1800 cm-1, indicated a relative concentration variation of MHC class I. PCA analysis was also performed to distinguish control and stressed cells within different cell lines. These mechanical induced phenotypic changes increase the tumor immunogenicity, as revealed by the related increased susceptibility to Natural Killer (NK) cells cytotoxic recognition.
U2 - 10.1371/journal.pone.0111758
DO - 10.1371/journal.pone.0111758
M3 - Journal article
C2 - 25541692
SN - 1932-6203
JO - P L o S One
JF - P L o S One
ER -