TY - JOUR
T1 - AFM study
T2 - Cell cycle and probe geometry influences nanomechanical characterization of Panc1 cells
AU - Kulkarni, Tanmay
AU - Tam, Alex
AU - Mukhopadhyay, Debabrata
AU - Bhattacharya, Santanu
N1 - Funding Information:
This work is partly supported by National Institutes of Health grants CA78383 , CA150190 (DM), Florida Department of Health (Cancer Research Chair Fund, Florida #3J to DM), Mayo Clinic Pancreatic Cancer SPORE Career Enhancement Award (SB). Appendix A
Funding Information:
This work is partly supported by National Institutes of Health grants CA78383, CA150190 (DM), Florida Department of Health (Cancer Research Chair Fund, Florida #3J to DM), Mayo Clinic Pancreatic Cancer SPORE Career Enhancement Award (SB).
Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/5
Y1 - 2019/5
N2 - Atomic force microscope (AFM) is emerging as an immensely promising tool to study the cellular morphology with a nanometer scale resolution and to analyze nanomechanical properties (NPs) at various physiological conditions. Advancement of AFM technology enables studying living cells and differentiating cancer cell from normal cells based on topography and NPs. Though the trend overlaps from different literature; numerical values of nanomechanical readouts depict variations over a wide range. These anomalies are associated with the experimental setup under study. In this manuscript, we have identified heterogeneity in cell culture system in addition to the selection of AFM probe with specific tip geometry as the major contributors to the above mentioned anomalies. To test our hypothesis, we have used Panc1 cells, which is a pancreatic ductal adenocarcinoma cell type. Our results suggest that the cellular morphology, membrane roughness and NPs calculated from AFM study are distinctly influenced by cell cycle. Furthermore, we found that the NPs readout is also significantly associated with AFM tip geometries. The cells were found to be softer in their early resting phase when indented with pyramidal probe and became increasingly stiffer as they progressed through the cell cycles. On the contrary, when indented with the spherical probe, cells in G0/G1 phase were observed to be the stiffest. Such an exhaustive study of the role of cell cycle in influencing the NPs in Panc1 cell line along with the impact of tip geometry on NPs is the first of its kind, to the best of our knowledge.
AB - Atomic force microscope (AFM) is emerging as an immensely promising tool to study the cellular morphology with a nanometer scale resolution and to analyze nanomechanical properties (NPs) at various physiological conditions. Advancement of AFM technology enables studying living cells and differentiating cancer cell from normal cells based on topography and NPs. Though the trend overlaps from different literature; numerical values of nanomechanical readouts depict variations over a wide range. These anomalies are associated with the experimental setup under study. In this manuscript, we have identified heterogeneity in cell culture system in addition to the selection of AFM probe with specific tip geometry as the major contributors to the above mentioned anomalies. To test our hypothesis, we have used Panc1 cells, which is a pancreatic ductal adenocarcinoma cell type. Our results suggest that the cellular morphology, membrane roughness and NPs calculated from AFM study are distinctly influenced by cell cycle. Furthermore, we found that the NPs readout is also significantly associated with AFM tip geometries. The cells were found to be softer in their early resting phase when indented with pyramidal probe and became increasingly stiffer as they progressed through the cell cycles. On the contrary, when indented with the spherical probe, cells in G0/G1 phase were observed to be the stiffest. Such an exhaustive study of the role of cell cycle in influencing the NPs in Panc1 cell line along with the impact of tip geometry on NPs is the first of its kind, to the best of our knowledge.
KW - Atomic force microscopy
KW - Cell cycle
KW - Nanoindentation
KW - Pancreatic cancer
KW - Young's modulus
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U2 - 10.1016/j.bbagen.2019.02.006
DO - 10.1016/j.bbagen.2019.02.006
M3 - Article
C2 - 30763604
AN - SCOPUS:85061660924
SN - 0304-4165
VL - 1863
SP - 802
EP - 812
JO - Biochimica et Biophysica Acta - General Subjects
JF - Biochimica et Biophysica Acta - General Subjects
IS - 5
ER -