TCells: Two-Photon Data: T Cells in a Lymph Node

In MotilityLab: Quantitative Analysis of Motion

Description

Labelled T cells were adoptively transfered and intravitally imaged (using two-photon microscopy) inside a peripheral lymph node of the recipient mouse. These data represent the characteristic "random-walk-like" motion pattern of T cells in lymph nodes.

Usage

data("TCells")

Format

An S3 object of class "tracks"; a list with 22 elements. Each element name identifies a cell track. Each element is a matrix containing the following four columns.

t

the time (in seconds)

x

The X coordinate (in micrometers)

y

The Y coordinate (in micrometers)

z

The Z coordinate (in micrometers)

Source

Data were generated in 2012 in the Mark J. Miller Lab, Department of Medicine, Washington University in St Louis, USA.

References

Zinselmeyer BH, Dempster J, Wokosin DL, Cannon JJ, Pless R, Parker I and Miller MJ (2009), Two-photon microscopy and multi-dimensional analysis of cell dynamics. Methods in Enzymology, 461:349–78. doi:10.1016/S0076-6879(09)05416-0

Konjufca V and Miller MJ (2009), Imaging Listeria monocytogenes infection in vivo. Current Topics in Microbiology and Immunology, 334:199–226. doi:10.1007/978-3-540-93864-4_9

Kreisel D, Nava RG, Li W, Zinselmeyer BH, Wang B, Lai J, Pless R, Gelman AE, Krupnick AS, and Miller MJ (2010), In vivo two-photon imaging reveals monocyte-dependent neutrophil extravasation during pulmonary inflammation. PNAS, 107(42):18073–18078. doi:10.1073/pnas.1008737107

Examples

## load the tracks
data(TCells)
## visualize the tracks (calls function plot.tracks)
plot(TCells)

Example output

MotilityLab documentation built on May 2, 2019, 8:31 a.m.