Real-time and quantitative measurement method for cell traction force
A real time and quantitative method of measuring traction force of living cells include the following procedures. Place AT-cut and BT-cut quartz crystals of the same frequency, surface morphology and/or modified with the same cell adhesion molecules in petri dishes or detection cells; add the cells to the petri dishes or detection cells, the cell traction force at arbitrary time t during adhesion of the cells or under different internal/external environmental stimulations is estimated by the following equation: ΔS t =(K AT −K BT ) −1 [t q AT Δf t AT /fr AT −tq BT Δf t BT /fr BT ]. The method can be used to track the dynamic changes of cells generated force during the adhesion of cells and under different internal/external environmental stimulations, such as the effects of drugs. The drugs can be added before or after the adhesion of the cells. This method is suitable for all adherent cells, including primary cells and passage cells.
1. A real-time and quantitative measurement method for cell traction force, comprising the following steps:
(1) placing an AT-cut quartz crystal and a BT-cut quartz crystal in culture dishes or detection cells, wherein the AT-cut quartz crystal having the same frequency, surface morphology and/or modified surface adhesion molecules as those of the BT-cut quartz crystal; and
(2) adding cells to be tested to the culture dishes or the detection cells, and measuring the cell traction force ΔS t of the cells at an adhesion time t by the following formula:
Δ S t =( K AT −K BT ) −1 [ t q AT Δf t AT /fr AT −tq BT Δf t BT /fr BT ] (1),
wherein K AT =2.75×10 −12 cm 2 dyn −1 and K BT =−2.65×10 −12 cm 2 dyn −1 are stress coefficients of the AT-cut quartz crystal and the BT-cut quartz crystal respectively; fr AT is the resonant frequency of the AT-cut quartz crystal, fr BT is the resonant frequency of the BT-cut quartz crystal, tq AT is the thickness of the AT-cut quartz crystal, tq BT is the thickness of the BT-cut quartz crystal, and all of which are constants; Δf t AT and Δf t BT are the frequency shifts of the AT-cut and BT-cut quartz crystals at any time t relative to their reference points respectively;
when ΔS t is negative, it indicates that the stress on the cells is a compressive stress, the cells are contracted, and the corresponding extracellular matrices are subjected to a tensile stress equal and opposite to the compressive stress; when ΔS t is positive, the stress on the cells is a tensile stress, the cells are spread, and the corresponding extracellular matrices are subjected to a compressive stress equal and opposite to the tensile stress.
2. The method according to claim 1 , wherein the cell adhesion molecules comprise extracellular matrix molecules capable of interacting with transmembrane proteins and integrins; extracellular matrix biomimetic molecules capable of interacting with transmembrane proteins and integrins; molecules capable of interacting with cell surface receptors; and molecules interacting with the surface of cells to promote cell adhesion.
3. The method according to claim 2 , wherein the extracellular matrix molecules capable of interacting with transmembrane proteins and integrins are fibronectin, laminin, vitronectin or collagen; the extracellular matrix biomimetic molecules capable of interacting with transmembrane proteins and integrins are RGD adhesion sequence polypeptides; the molecules capable of interacting with cell surface receptors are molecules capable of interacting with cell surface cadherin; and the molecules interacting with the surface of cells to promote cell adhesion are poly-l-lysine.
4. The method according to claim 1 , wherein in the formula of step (2), t q AT =0.1661/fr AT ; and t q BT =0.2536/f r BT .