| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Biomedical Engineering Department, Boston University, Boston, Massachusetts 02215
Correspondence: Address reprint requests to Micah Dembo, 44 Cummington St., Boston University, Boston, MA 02215. Tel.: 617-353-1671; Fax: 617-353-6766; E-mail: mxd{at}bu.edu.
Much experimental data exist on the mechanical properties of neutrophils, but so far, they have mostly been approached within the framework of liquid droplet models. This has two main drawbacks: 1), It treats the cytoplasm as a single phase when in reality, it is a composite of cytosol and cytoskeleton; and 2), It does not address the problem of active neutrophil deformation and force generation. To fill these lacunae, we develop here a comprehensive continuum-mechanical paradigm of the neutrophil that includes proper treatment of the membrane, cytosol, and cytoskeleton components. We further introduce two models of active force production: a cytoskeletal swelling force and a polymerization force. Armed with these tools, we present computer simulations of three classic experiments: the passive aspiration of a neutrophil into a micropipette, the active extension of a pseudopod by a neutrophil exposed to a local stimulus, and the crawling of a neutrophil inside a micropipette toward a chemoattractant against a varying counterpressure. Principal results include: 1), Membrane cortical tension is a global property of the neutrophil that is affected by local area-increasing shape changes. We argue that there exists an area dilation viscosity caused by the work of unfurling membrane-storing wrinkles and that this viscosity is responsible for much of the regulation of neutrophil deformation. 2), If there is no swelling force of the cytoskeleton, then it must be endowed with a strong cohesive elasticity to prevent phase separation from the cytosol during vigorous suction into a capillary tube. 3), We find that both swelling and polymerization force models are able to provide a unifying fit to the experimental data for the three experiments. However, force production required in the polymerization model is beyond what is expected from a simple short-range Brownian ratchet model. 4), It appears that, in the crawling of neutrophils or other amoeboid cells inside a micropipette, measurement of velocity versus counterpressure curves could provide a determination of whether cytoskeleton-to-cytoskeleton interactions (such as swelling) or cytoskeleton-to-membrane interactions (such as polymerization force) are predominantly responsible for active protrusion.
This article has been cited by other articles:
![]() |
C. W. Wolgemuth Collective Swimming and the Dynamics of Bacterial Turbulence Biophys. J., August 15, 2008; 95(4): 1564 - 1574. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Kapustina, G. E. Weinreb, N. Costigliola, Z. Rajfur, K. Jacobson, and T. C. Elston Mechanical and Biochemical Modeling of Cortical Oscillations in Spreading Cells Biophys. J., June 15, 2008; 94(12): 4605 - 4620. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zajac, B. Dacanay, W. A. Mohler, and C. W. Wolgemuth Depolymerization-Driven Flow in Nematode Spermatozoa Relates Crawling Speed to Size and Shape Biophys. J., May 15, 2008; 94(10): 3810 - 3823. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Prass, K. Jacobson, A. Mogilner, and M. Radmacher Direct measurement of the lamellipodial protrusive force in a migrating cell J. Cell Biol., September 11, 2006; 174(6): 767 - 772. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Herant, V. Heinrich, and M. Dembo Mechanics of neutrophil phagocytosis: experiments and quantitative models. J. Cell Sci., May 1, 2006; 119(Pt 9): 1903 - 1913. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Rosenbluth, W. A. Lam, and D. A. Fletcher Force Microscopy of Nonadherent Cells: A Comparison of Leukemia Cell Deformability Biophys. J., April 15, 2006; 90(8): 2994 - 3003. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. W. Wolgemuth Lamellipodial Contractions during Crawling and Spreading Biophys. J., September 1, 2005; 89(3): 1643 - 1649. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Herant, V. Heinrich, and M. Dembo Mechanics of neutrophil phagocytosis: behavior of the cortical tension J. Cell Sci., May 1, 2005; 118(9): 1789 - 1797. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. W. Wolgemuth, L. Miao, O. Vanderlinde, T. Roberts, and G. Oster MSP Dynamics Drives Nematode Sperm Locomotion Biophys. J., April 1, 2005; 88(4): 2462 - 2471. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Jadhav, C. D. Eggleton, and K. Konstantopoulos A 3-D Computational Model Predicts that Cell Deformation Affects Selectin-Mediated Leukocyte Rolling Biophys. J., January 1, 2005; 88(1): 96 - 104. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. B. Lomakina, C. M. Spillmann, M. R. King, and R. E. Waugh Rheological Analysis and Measurement of Neutrophil Indentation Biophys. J., December 1, 2004; 87(6): 4246 - 4258. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Yanai, J. P. Butler, T. Suzuki, H. Sasaki, and H. Higuchi Regional rheological differences in locomoting neutrophils Am J Physiol Cell Physiol, September 1, 2004; 287(3): C603 - C611. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Huang, R. D. Kamm, and R. T. Lee Cell mechanics and mechanotransduction: pathways, probes, and physiology Am J Physiol Cell Physiol, July 1, 2004; 287(1): C1 - C11. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Chodniewicz, A. M. Alteraifi, and D. V. Zhelev Experimental Evidence for the Limiting Role of Enzymatic Reactions in Chemoattractant-induced Pseudopod Extension in Human Neutrophils J. Biol. Chem., June 4, 2004; 279(23): 24460 - 24466. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |