1 July 2006 Observation of dynamic subdomains in red blood cells
Author Affiliations +
J. of Biomedical Optics, 11(4), 040503 (2006). doi:10.1117/1.2221867
We quantify the nanoscale structure and low-frequency dynamics associated with live red blood cells. The membrane displacements are measured using quantitative phase images provided by Fourier phase microscopy, with an average path-length stability of 0.75 nm over 45 min. The results reveal the existence of dynamic, independent subdomains across the cells that fluctuate at various dominant frequencies.
Popescu, Badizadegan, and Dasari: Observation of dynamic subdomains in red blood cells

Red blood cells (RBCs) lack nuclei and major organelles, and thus provide a convenient model for studying the dynamical properties of cells and the cytoskeleton. AFM has emerged as a high-resolution technique for structural analysis of minimally fixed erythrocytes.1 Although quantitative, AFM samples one single point at a time, requires contact, and is technically limited when applied to soft structures such as membranes of mammalian cells.

RBC “flickering”—spontaneous membrane fluctuations—was first observed more than a century ago. These submicron motions are characterized by membrane displacements that take place at the millisecond scale or less. Significant progress has been made in modeling this phenomenon and connecting mechanical properties of the cell to the statistical properties of these fluctuations. 2, 3, 4, 5 It has been suggested that thermal excitation does not entirely explain these motions and that a deterministic component exists that may in fact accomplish certain physiological tasks, such as improving cell flexibility and filterability.2, 6 More recently, based on theoretical modeling and simulation, it has been suggested that the thermal fluctuations of the membrane regulate protein mobility.7 Experimental work on quantifying such intrinsic cellular fluctuations has been limited, due to the lack of noninvasive imaging techniques for quantifying nanoscale membrane fluctuations.

Phase contrast microscopy has been used to study spatially-resolved RBC fluctuations.2, 8 However, the relationship between the detected intensity and the cell thickness is nonlinear; thus, the phase contrast technique is essentially restricted to qualitative investigations. Reflection interference contrast (RIC) microscopy was developed to quantify the thermally-induced fluctuations of the erythrocyte membrane.9 As with phase contrast, RIC is quantitative only in certain limiting situations.10 In point dark field microscopy, undulations of the cell are quantified by detecting the displacements of the cell edge.11 This technique was used to demonstrate the effect of adenosine tri-phosphate (ATP) on RBC membrane dynamics, but it allows only for point measurements and is not suitable for studying subtle, spatial behavior of fluctuations.

Recently, quantitative phase imaging has been shown to have direct applicability in studying RBC structure and dynamics.12, 13, 14 Fourier phase microscopy (FPM) has been developed in our laboratory as a highly sensitive quantitative phase imaging technique with high transverse resolution.15 Due to its subnanometer path-length stability over many hours, FPM is very well suited for studying slow (seconds to days) phenomena in cell biology. In particular, this measurement technique is ideal for quantifying nanoscale RBC structure and fluctuations, as the cells can be assumed to be optically homogeneous, i.e., the local phase shift produced by the cells is linearly proportional to their thickness.10

The FPM experimental arrangement is described in detail elsewhere.15 The technique is based on describing image formation as an interference phenomenon and combines phase-contrast microscopy and phase-shifting interferometry. The phase shifting and data acquisition are synchronized and fully controllable by a computer. The FPM acquisition rate is limited by the refresh rate of the liquid crystal modulator, which is 7 to 8Hz .15 Thus the technique allows the study of nanoscale structure and slow (minutes) dynamics of live RBCs with high-transverse resolution and subnanometer path-length sensitivity over long periods of time. Fresh human blood sandwiched between two cover slips was directly imaged by FPM, using a 40×(0.65NA) objective. For the illumination wavelength used (λ=821nm) , we assumed the cells to be characterized by a constant refractive index nc=1.41 and the surrounding plasma by np=1.34 .16 The quantitative phase image retrieved, ϕ(x,y) , was transformed to provide the thickness profile of red blood cells, h(x,y)=λϕ(x,y)[2π(ncnp)] . Figure 1 shows a map h(x,y) retrieved from an entire whole blood smear, where the normal discoid shape of the cells is clearly resolved in a quantitative manner. In order to study the low-frequency dynamics of live cells, we acquired full-field phase images for 45min at a repetition rate of 2framesmin . The stability of the technique against the inherent phase noise was established by measuring the path-length fluctuations associated with a region containing no cells [indicated by the rectangular region in Fig. 1a]. Figure 1b shows the histogram of path-length standard deviations σ associated with the pixels in this region. Remarkably, the average standard deviation has a value of 0.75nm , without performing time-averaging. The only other technique that can achieve such remarkable z -axis displacement sensitivity is AFM. However FPM, being a full-field, noncontact, preparation-free technique, provides unique advantages for live cell studies.

Fig. 1

(a) FPM image of a whole blood smear (red scale). The color bar indicates the cell thickness in microns (color online only). (b) Histogram of optical path-length standard deviation associated with pixels in the rectangular area indicated in (a).


For analysis of cell dynamics, individual cells were segmented from the background using a computer routine developed in-house. Typically, cells exhibit transverse motion of the order of a micron or less. These translational movements were suppressed by tracking the cell centroid. Thus, time series of individual cell fluctuations were obtained over the period of observation. These datasets contain detailed four-dimensional (x,y,h;t) information about the cell dynamics. Figure 2b shows the temporal fluctuations of the cell displacement associated with the points indicated in Fig. 2a. Water transport through the membrane due to osmolarity instability can potentially modify the cell optical path length and, thus, introduce errors in the fluctuation measurement.17 In order to demonstrate that the signals shown in Fig. 2b are free from such effects, we measured temporal fluctuations of the average cell thickness [solid curve in Fig. 2b]. The fact that this curve is essentially flat demonstrates that, overall, there are no volume changes associated with the cell and the path-length fluctuations are due to membrane displacements. Remarkably, moving from the center of the cell toward the rim, the fluctuations appear to be characterized by a progressively increasing standard deviation. In addition, the time-varying traces extracted exhibit clear periodic components, with various dominant frequencies. The spatially-resolved temporal autocorrelation function is defined as


Thus, the power spectrum P(x,y;ω) of the fluctuations in each point of the image is simply obtained by Fourier transforming the autocorrelation function,


In order to characterize the cell fluctuations in a spatially-resolved manner, the entire cell was mapped out in terms of the average frequency of fluctuation f¯ ,


Figure 2c shows this map and suggests that the cell can be divided into areas of independent dynamics with different average oscillation frequencies. These results may be due to specific biochemical domains within the cytoskeleton or plasma membrane (e.g., lipid rafts). Figure 2d depicts the average frequency map associated with the rectangular background area shown in Fig. 1a. This map is essentially uniform and demonstrates that the frequency map of Fig. 2c is directly related to the dynamic motion of the cell membrane. Such low-frequency cell dynamics may be related to active (ATP-assisted) processes within the cell. Similarly, although within different frequency ranges, recent studies involving AFM4 and interference microscopy18 identified unexpected distinct modes of fluctuations in bacteria and neurons, respectively. This type of nanometer scale cellular dynamics should be highly relevant in understanding the processes that regulate cell metabolism. Quantifying membrane fluctuations should also provide information about the mechanical properties of the membrane-cytoskeleton ensemble.

Fig. 2

(a) Spatially-resolved dynamics of the cell. (b) Temporal cell thickness fluctuations associated with the selected points indicated in (a); the corresponding standard deviations σ are indicated. Similar data is obtained for every point in the image (not shown). The solid line shows the fluctuation of the average cell thickness (shifted down by 500nm , to inhance visibility). (c) Whole cell map of the average fluctuation frequency, calculated from the measured power spectrum of membrane fluctuations. The color bar indicates the mean frequency in inverse minutes (color online only). High values at the cell edges are due to transverse motions. High values in the center of the cell indicate high-frequency dynamic domains. (d) Average frequency map of the region indicated in Fig. 1a.


In summary, we measured noncontact, spatially-resolved, quantitative nanoscale red blood cell membrane fluctuations. The results demonstrate the existence of low-frequency fluctuations across the cells, which develop in isolated subdomains. These motions may be caused by nonrandom sources, such as metabolic processes within the cell. To our knowledge, this type of slow cell membrane dynamics has been reported here for the first time. Current work in our laboratory is directed toward understanding the effect of ATP to the possibly deterministic membrane motion.


This work was carried out at the MIT Laser Biomedical Research Center, supported by NIH P41 RR 02594 and partially by Hamamatsu Photonics K.K.


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Gabriel Popescu, Kamran Badizadegan, Ramachandra R. Dasari, Michael S. Feld, "Observation of dynamic subdomains in red blood cells," Journal of Biomedical Optics 11(4), 040503 (1 July 2006). http://dx.doi.org/10.1117/1.2221867



Phase measurement

Atomic force microscopy

Phase contrast

Acquisition tracking and pointing


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