Nanomagnetic actuation of receptor-mediated signal transduction

被引:260
作者
Mannix, Robert J. [1 ,2 ,3 ]
Kumar, Sanjay [1 ,2 ,3 ,4 ]
Cassiola, Flavia [1 ,2 ,3 ]
Montoya-Zavala, Martin [1 ,2 ,3 ]
Feinstein, Efraim [5 ]
Prentiss, Mara [5 ]
Ingber, Donald E. [1 ,2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Vasc Biol Program, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Vasc Biol Program, Dept Surg, Boston, MA 02115 USA
[3] Childrens Hosp, Boston, MA 02115 USA
[4] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[5] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
关键词
D O I
10.1038/nnano.2007.418
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Complex cell behaviours are triggered by chemical ligands that bind to membrane receptors and alter intracellular signal transduction. However, future biosensors, medical devices and other microtechnologies that incorporate living cells as system components will require actuation mechanisms that are much more rapid, robust, non-invasive and easily integrated with solid-state interfaces. Here we describe a magnetic nanotechnology that activates a biochemical signalling mechanism normally switched on by binding of multivalent chemical ligands. Superparamagnetic 30-nm beads, coated with monovalent ligands and bound to transmembrane receptors, magnetize when exposed to magnetic fields, and aggregate owing to bead-bead attraction in the plane of the membrane. Associated clustering of the bound receptors acts as a nanomagnetic cellular switch that directly transduces magnetic inputs into physiological cellular outputs, with rapid system responsiveness and non-invasive dynamic control. This technique may represent a new actuator mechanism for cell-based microtechnologies and man-machine interfaces.
引用
收藏
页码:36 / 40
页数:5
相关论文
共 23 条
[1]   The immunological synapse [J].
Bromley, SK ;
Burack, WR ;
Johnson, KG ;
Somersalo, K ;
Sims, TN ;
Sumen, C ;
Davis, MM ;
Shaw, AS ;
Allen, PM ;
Dustin, ML .
ANNUAL REVIEW OF IMMUNOLOGY, 2001, 19 :375-396
[2]   Iron oxide MR contrast agents for molecular and cellular imaging [J].
Bulte, JWM ;
Kraitchman, DL .
NMR IN BIOMEDICINE, 2004, 17 (07) :484-499
[3]   A NEURON-SILICON JUNCTION - A RETZIUS CELL OF THE LEECH ON AN INSULATED-GATE FIELD-EFFECT TRANSISTOR [J].
FROMHERZ, P ;
OFFENHAUSSER, A ;
VETTER, T ;
WEIS, J .
SCIENCE, 1991, 252 (5010) :1290-1293
[4]   MAGNETIC-FIELDS APPLIED TO COLLAGEN-COATED FERRIC-OXIDE BEADS INDUCE STRETCH-ACTIVATED CA2+ FLUX IN FIBROBLASTS [J].
GLOGAUER, M ;
FERRIER, J ;
MCCULLOCH, CAG .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 269 (05) :C1093-C1104
[5]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[6]   Heteromultimerization and NMDA receptor-clustering activity of chapsyn-110, a member of the PSD-95 family of proteins [J].
Kim, E ;
Cho, KO ;
Rothschild, A ;
Sheng, M .
NEURON, 1996, 17 (01) :103-113
[7]   Brain cancer diagnosis and therapy with nanoplatforms [J].
Koo, Yong-Eun Lee ;
Reddy, G. Ramachandra ;
Bhojani, Mahaveer ;
Schneider, Randy ;
Philbert, Martin A. ;
Rehemtulla, Alnawaz ;
Ross, Brian D. ;
Kopelman, Raoul .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (14) :1556-1577
[8]   gp49B1 inhibits IgE-initiated mast cell activation through both immunoreceptor tyrosine-based inhibitory motifs, recruitment of src homology 2 domain-containing phosphatase-1, and suppression of early and late calcium mobilization [J].
Lu-Kuo, JM ;
Joyal, DM ;
Austen, KF ;
Katz, HR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (09) :5791-5796
[9]   Cellular adaptation to mechanical stress: role of integrins, Rho, cytoskeletal tension and mechanosensitive ion channels [J].
Matthews, BD ;
Overby, DR ;
Mannix, R ;
Ingber, DE .
JOURNAL OF CELL SCIENCE, 2006, 119 (03) :508-518
[10]   Electromagnetic needles with submicron pole tip radii for nanomanipulation of biomolecules and living cells [J].
Matthews, BD ;
LaVan, DA ;
Overby, DR ;
Karavitis, J ;
Ingber, DE .
APPLIED PHYSICS LETTERS, 2004, 85 (14) :2968-2970