Cell imaging with the widefield surface plasmon microscope

M. M.Abdul Jamil, F. Sefat, S. A. Khaghani, S. B. Lobo, F. A. Javid, M. Youseffi, S. T. Britland, S. G. Liu, C. W. See, M. G. Somekh, M. C.T. Denyer

Research output: Chapter in Book/Report/Conference proceedingConference contribution

5 Citations (Scopus)

Abstract

Imaging interfacial environment has proved challenging using standard imaging systems. This is a problem that may be circumvented using the widefield surface plasmon microscope (WSPR). Surface plasmon microscopy relies on the excitation of electron oscillations at a conductor/dielectric interface by P polarised light striking that interface at a specific surface plasmon resonance (SPR) angle. The SPR angle can be changed by application of a molecular species to the conductor, which modifies the mean refractive index at that interface and thus alters the coupling efficiency between the conductor and the P-polarised light. Commercial SPR microscopes unfortunately have poor lateral resolutions, but the WSPR uses a high numerical aperture lens to excite surface plasmons, and thus not only enables nanometric Z axes imaging of interfacial molecular interactions but also enables SPR imaging at micron to submicron lateral resolutions. Initial work has shown that this system can be used to image cell/surface interactions. This paper focuses on looking at the use of the WSPR microscope in the imaging of a human keratinocyte cell line (HaCat cells), bone cells, neonatal rat intestinal smooth muscle cells and neonatal rat knee joint derived chondrocytes. Of these cell types the HaCat cells couple tightly to the cell culture surface, and this is reflected by clear band like arrangements of focal contacts, in comparison chondrocytes, smooth muscle cells and bone cells couple less strongly to the surface and this is reflected by less clearly defined arrangements of focal contacts. In all cases WSPR microscopy also enabled identification of internal cellular features, specifically the nucleus and in the case of smooth muscle cells contractile filament like structures.

LanguageEnglish
Title of host publication4th Kuala Lumpur International Conference on Biomedical Engineering 2008, Biomed 2008
Pages528-531
Number of pages4
Volume21 IFMBE
Edition1
DOIs
Publication statusPublished - 1 Dec 2008
Externally publishedYes
Event4th Kuala Lumpur International Conference on Biomedical Engineering - Kuala Lumpur, Malaysia
Duration: 25 Jun 200828 Jun 2008
Conference number: 4

Conference

Conference4th Kuala Lumpur International Conference on Biomedical Engineering
Abbreviated titleBIOMED 2008
CountryMalaysia
CityKuala Lumpur
Period25/06/0828/06/08

Fingerprint

Microscopes
Imaging techniques
Surface plasmon resonance
Cells
Muscle
Light polarization
Rats
Microscopic examination
Bone
Plasmons
Molecular interactions
Cell culture
Imaging systems
Lenses
Refractive index
Electrons

Cite this

Jamil, M. M. A., Sefat, F., Khaghani, S. A., Lobo, S. B., Javid, F. A., Youseffi, M., ... Denyer, M. C. T. (2008). Cell imaging with the widefield surface plasmon microscope. In 4th Kuala Lumpur International Conference on Biomedical Engineering 2008, Biomed 2008 (1 ed., Vol. 21 IFMBE, pp. 528-531) https://doi.org/10.1007/978-3-540-69139-6_132
Jamil, M. M.Abdul ; Sefat, F. ; Khaghani, S. A. ; Lobo, S. B. ; Javid, F. A. ; Youseffi, M. ; Britland, S. T. ; Liu, S. G. ; See, C. W. ; Somekh, M. G. ; Denyer, M. C.T. / Cell imaging with the widefield surface plasmon microscope. 4th Kuala Lumpur International Conference on Biomedical Engineering 2008, Biomed 2008. Vol. 21 IFMBE 1. ed. 2008. pp. 528-531
@inproceedings{cd9f95d2d0114ba099e4dade5470fbf4,
title = "Cell imaging with the widefield surface plasmon microscope",
abstract = "Imaging interfacial environment has proved challenging using standard imaging systems. This is a problem that may be circumvented using the widefield surface plasmon microscope (WSPR). Surface plasmon microscopy relies on the excitation of electron oscillations at a conductor/dielectric interface by P polarised light striking that interface at a specific surface plasmon resonance (SPR) angle. The SPR angle can be changed by application of a molecular species to the conductor, which modifies the mean refractive index at that interface and thus alters the coupling efficiency between the conductor and the P-polarised light. Commercial SPR microscopes unfortunately have poor lateral resolutions, but the WSPR uses a high numerical aperture lens to excite surface plasmons, and thus not only enables nanometric Z axes imaging of interfacial molecular interactions but also enables SPR imaging at micron to submicron lateral resolutions. Initial work has shown that this system can be used to image cell/surface interactions. This paper focuses on looking at the use of the WSPR microscope in the imaging of a human keratinocyte cell line (HaCat cells), bone cells, neonatal rat intestinal smooth muscle cells and neonatal rat knee joint derived chondrocytes. Of these cell types the HaCat cells couple tightly to the cell culture surface, and this is reflected by clear band like arrangements of focal contacts, in comparison chondrocytes, smooth muscle cells and bone cells couple less strongly to the surface and this is reflected by less clearly defined arrangements of focal contacts. In all cases WSPR microscopy also enabled identification of internal cellular features, specifically the nucleus and in the case of smooth muscle cells contractile filament like structures.",
keywords = "cell imaging, interfaces, Surface plasmon",
author = "Jamil, {M. M.Abdul} and F. Sefat and Khaghani, {S. A.} and Lobo, {S. B.} and Javid, {F. A.} and M. Youseffi and Britland, {S. T.} and Liu, {S. G.} and See, {C. W.} and Somekh, {M. G.} and Denyer, {M. C.T.}",
year = "2008",
month = "12",
day = "1",
doi = "10.1007/978-3-540-69139-6_132",
language = "English",
isbn = "9783540691389",
volume = "21 IFMBE",
pages = "528--531",
booktitle = "4th Kuala Lumpur International Conference on Biomedical Engineering 2008, Biomed 2008",
edition = "1",

}

Jamil, MMA, Sefat, F, Khaghani, SA, Lobo, SB, Javid, FA, Youseffi, M, Britland, ST, Liu, SG, See, CW, Somekh, MG & Denyer, MCT 2008, Cell imaging with the widefield surface plasmon microscope. in 4th Kuala Lumpur International Conference on Biomedical Engineering 2008, Biomed 2008. 1 edn, vol. 21 IFMBE, pp. 528-531, 4th Kuala Lumpur International Conference on Biomedical Engineering , Kuala Lumpur, Malaysia, 25/06/08. https://doi.org/10.1007/978-3-540-69139-6_132

Cell imaging with the widefield surface plasmon microscope. / Jamil, M. M.Abdul; Sefat, F.; Khaghani, S. A.; Lobo, S. B.; Javid, F. A.; Youseffi, M.; Britland, S. T.; Liu, S. G.; See, C. W.; Somekh, M. G.; Denyer, M. C.T.

4th Kuala Lumpur International Conference on Biomedical Engineering 2008, Biomed 2008. Vol. 21 IFMBE 1. ed. 2008. p. 528-531.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

TY - GEN

T1 - Cell imaging with the widefield surface plasmon microscope

AU - Jamil, M. M.Abdul

AU - Sefat, F.

AU - Khaghani, S. A.

AU - Lobo, S. B.

AU - Javid, F. A.

AU - Youseffi, M.

AU - Britland, S. T.

AU - Liu, S. G.

AU - See, C. W.

AU - Somekh, M. G.

AU - Denyer, M. C.T.

PY - 2008/12/1

Y1 - 2008/12/1

N2 - Imaging interfacial environment has proved challenging using standard imaging systems. This is a problem that may be circumvented using the widefield surface plasmon microscope (WSPR). Surface plasmon microscopy relies on the excitation of electron oscillations at a conductor/dielectric interface by P polarised light striking that interface at a specific surface plasmon resonance (SPR) angle. The SPR angle can be changed by application of a molecular species to the conductor, which modifies the mean refractive index at that interface and thus alters the coupling efficiency between the conductor and the P-polarised light. Commercial SPR microscopes unfortunately have poor lateral resolutions, but the WSPR uses a high numerical aperture lens to excite surface plasmons, and thus not only enables nanometric Z axes imaging of interfacial molecular interactions but also enables SPR imaging at micron to submicron lateral resolutions. Initial work has shown that this system can be used to image cell/surface interactions. This paper focuses on looking at the use of the WSPR microscope in the imaging of a human keratinocyte cell line (HaCat cells), bone cells, neonatal rat intestinal smooth muscle cells and neonatal rat knee joint derived chondrocytes. Of these cell types the HaCat cells couple tightly to the cell culture surface, and this is reflected by clear band like arrangements of focal contacts, in comparison chondrocytes, smooth muscle cells and bone cells couple less strongly to the surface and this is reflected by less clearly defined arrangements of focal contacts. In all cases WSPR microscopy also enabled identification of internal cellular features, specifically the nucleus and in the case of smooth muscle cells contractile filament like structures.

AB - Imaging interfacial environment has proved challenging using standard imaging systems. This is a problem that may be circumvented using the widefield surface plasmon microscope (WSPR). Surface plasmon microscopy relies on the excitation of electron oscillations at a conductor/dielectric interface by P polarised light striking that interface at a specific surface plasmon resonance (SPR) angle. The SPR angle can be changed by application of a molecular species to the conductor, which modifies the mean refractive index at that interface and thus alters the coupling efficiency between the conductor and the P-polarised light. Commercial SPR microscopes unfortunately have poor lateral resolutions, but the WSPR uses a high numerical aperture lens to excite surface plasmons, and thus not only enables nanometric Z axes imaging of interfacial molecular interactions but also enables SPR imaging at micron to submicron lateral resolutions. Initial work has shown that this system can be used to image cell/surface interactions. This paper focuses on looking at the use of the WSPR microscope in the imaging of a human keratinocyte cell line (HaCat cells), bone cells, neonatal rat intestinal smooth muscle cells and neonatal rat knee joint derived chondrocytes. Of these cell types the HaCat cells couple tightly to the cell culture surface, and this is reflected by clear band like arrangements of focal contacts, in comparison chondrocytes, smooth muscle cells and bone cells couple less strongly to the surface and this is reflected by less clearly defined arrangements of focal contacts. In all cases WSPR microscopy also enabled identification of internal cellular features, specifically the nucleus and in the case of smooth muscle cells contractile filament like structures.

KW - cell imaging

KW - interfaces

KW - Surface plasmon

UR - http://www.scopus.com/inward/record.url?scp=78349297849&partnerID=8YFLogxK

U2 - 10.1007/978-3-540-69139-6_132

DO - 10.1007/978-3-540-69139-6_132

M3 - Conference contribution

SN - 9783540691389

VL - 21 IFMBE

SP - 528

EP - 531

BT - 4th Kuala Lumpur International Conference on Biomedical Engineering 2008, Biomed 2008

ER -

Jamil MMA, Sefat F, Khaghani SA, Lobo SB, Javid FA, Youseffi M et al. Cell imaging with the widefield surface plasmon microscope. In 4th Kuala Lumpur International Conference on Biomedical Engineering 2008, Biomed 2008. 1 ed. Vol. 21 IFMBE. 2008. p. 528-531 https://doi.org/10.1007/978-3-540-69139-6_132