Neutrophils display biphasic relationship between migration and substrate stiffness.

Neutrophils are one type of migrating cell in the body's innate immune system and are the first line of defense against inflammation or infection. While extensive work exists on the effect of adhesive proteins on neutrophil motility, little is known about how neutrophil motility is affected by the mechanical properties of their physical environment. This study investigated the effects of substrate stiffness on the morphology, random motility coefficient, track speed (v), spreading area, and distribution of turning angles of neutrophils during chemokinesis. Human neutrophils were plated onto polyacrylamide gels of varying stiffness, ranging from 3 to 13 kPa, and coated with the extracellular matrix protein fibronectin, and timelapse images were taken with phase contrast microscopy. Our results show a biphasic behavior between neutrophil motility and substrate stiffness, with the optimum stiffness for motility depending on the concentration of fibronectin on the surface of the gel. On 100 microg/mL fibronectin, the optimum stiffness is 4 kPa (v = 6.9 +/- 0.6 microm/min) while on 10 microg/mL fibronectin, the optimum stiffness increases to 7 kPa (v = 4.5 +/- 2.0 microm/min). This biphasic behavior most likely arises because neutrophils on soft gels are less adherent, preventing production of traction forces, while neutrophils on stiff gels adhere strongly, resulting in decreased migration. At intermediate stiffness, however, neutrophils can attain optimal motility as a function of extracellular matrix coating.

[1]  Shelly R. Peyton,et al.  Extracellular matrix rigidity governs smooth muscle cell motility in a biphasic fashion , 2005, Journal of cellular physiology.

[2]  P. Janmey,et al.  Effects of substrate stiffness on cell morphology, cytoskeletal structure, and adhesion. , 2005, Cell motility and the cytoskeleton.

[3]  Douglas A Lauffenburger,et al.  Microarchitecture of three-dimensional scaffolds influences cell migration behavior via junction interactions. , 2008, Biophysical journal.

[4]  S. Sen,et al.  Matrix Elasticity Directs Stem Cell Lineage Specification , 2006, Cell.

[5]  Devrim Pesen,et al.  Micromechanical architecture of the endothelial cell cortex. , 2005, Biophysical journal.

[6]  A. Huttenlocher,et al.  Regulation of integrin‐mediated adhesion during cell migration , 1998, Microscopy research and technique.

[7]  H. Aranda‐Espinoza,et al.  Cholesterol depletion increases membrane stiffness of aortic endothelial cells. , 2004, Biophysical journal.

[8]  R M Hochmuth,et al.  Mechanical anchoring strength of L-selectin, beta2 integrins, and CD45 to neutrophil cytoskeleton and membrane. , 1999, Biophysical journal.

[9]  Y. Wang,et al.  Preparation of a flexible, porous polyacrylamide substrate for mechanical studies of cultured cells. , 1998, Methods in enzymology.

[10]  W. Kraus,et al.  Endothelial, cardiac muscle and skeletal muscle exhibit different viscous and elastic properties as determined by atomic force microscopy. , 2001, Journal of biomechanics.

[11]  J. Pearson Vascular Adhesion Molecules and Inflammation , 2012, Progress in Inflammation Research.

[12]  Michael P. Sheetz,et al.  Two-piconewton slip bond between fibronectin and the cytoskeleton depends on talin , 2003, Nature.

[13]  L. Liotta,et al.  Molecular mediators of interactions with extracellular matrix components in metastasis and angiogenesis. , 1994, Current opinion in oncology.

[14]  Sandor Kasas,et al.  Deformation and height anomaly of soft surfaces studied with an AFM , 1993 .

[15]  M. Dembo,et al.  Neutrophil traction stresses are concentrated in the uropod during migration. , 2007, Biophysical journal.

[16]  J. Gunn,et al.  Adhesive and mechanical properties of hydrogels influence neurite extension. , 2005, Journal of biomedical materials research. Part A.

[17]  R D Stevenson,et al.  Dispersive locomotion of human neutrophils in response to a steroid-induced factor from monocytes. , 1994, Journal of cell science.

[18]  Y. Wang,et al.  Cell locomotion and focal adhesions are regulated by substrate flexibility. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[19]  C. Waterman-Storer,et al.  Spatiotemporal Feedback between Actomyosin and Focal-Adhesion Systems Optimizes Rapid Cell Migration , 2006, Cell.

[20]  Sean P. Palecek,et al.  Physical and biochemical regulation of integrin release during rear detachment of migrating cells. , 1998, Journal of cell science.

[21]  R. Pardi,et al.  Pathophysiology of leukocyte-tissue interactions. , 2006, Current opinion in cell biology.

[22]  W. Muller,et al.  Locomotion of monocytes on endothelium is a critical step during extravasation , 2004, Nature Immunology.

[23]  Paul Martin,et al.  Wound Healing--Aiming for Perfect Skin Regeneration , 1997, Science.

[24]  K. Nagayama,et al.  Local mechanical properties measured by atomic force microscopy for cultured bovine endothelial cells exposed to shear stress. , 2000, Journal of biomechanics.

[25]  R M Nerem,et al.  The application of a homogeneous half-space model in the analysis of endothelial cell micropipette measurements. , 1988, Journal of biomechanical engineering.

[26]  D. Hammer,et al.  Interplay between shear stress and adhesion on neutrophil locomotion. , 2007, Biophysical journal.

[27]  Lisa A Flanagan,et al.  Neurite branching on deformable substrates , 2002, Neuroreport.

[28]  Dennis Discher,et al.  Substrate compliance versus ligand density in cell on gel responses. , 2004, Biophysical journal.

[29]  H. Gruler,et al.  Analysis of cell movement. , 1984, Blood cells.

[30]  M. Dembo,et al.  Cell movement is guided by the rigidity of the substrate. , 2000, Biophysical journal.

[31]  Michael P. Sheetz,et al.  Rigidity Sensing at the Leading Edge through αvβ3 Integrins and RPTPα , 2006 .

[32]  D A Lauffenburger,et al.  Maximal migration of human smooth muscle cells on fibronectin and type IV collagen occurs at an intermediate attachment strength , 1993, The Journal of cell biology.

[33]  Joyce Y Wong,et al.  Neurite outgrowth and branching of PC12 cells on very soft substrates sharply decreases below a threshold of substrate rigidity , 2007, Journal of neural engineering.

[34]  S. Haskill,et al.  Signal transduction from the extracellular matrix , 1993, The Journal of cell biology.