Projects per year
Description
Description
Expression profiling by high throughput sequencing of ruminant (cattle and sheep) myeloid cells: 36 samples were profiled in total; derived from four biological replicates (i.e. isolated from four cattle or sheep). The myeloid subsets (of 4 individuals) were all derived from peripheral blood mononuclear cell preparations as follows:
Sheep: (a) monocytes - purified by CD14+ MACS separation; (b) monocyte derived dendritic cells - cultured CD14+ monocytes with ovine IL-4 & GMCSF; (c) monocyte derived macrophages (MDM) - cultured adherent cells; (d) Chlamydia infected MDM.
Cattle: (a) CD14+ monocytes - purified by CD14+ MACS separation; (b) CD16hi++ monocytes - purified by CD16+ MACS separation, followed by flow cytometry to obtain the CD16hi++ monocytes (c) monocyte derived dendritic cells - cultured CD14+ monocytes with bovine IL-4 & GMCSF; (d) monocyte derived macrophages (MDM) - cultured adherent cells; (e) Chlamydia infected MDM.
Expression profiling by high throughput sequencing of ruminant (cattle and sheep) myeloid cells: 36 samples were profiled in total; derived from four biological replicates (i.e. isolated from four cattle or sheep). The myeloid subsets (of 4 individuals) were all derived from peripheral blood mononuclear cell preparations as follows:
Sheep: (a) monocytes - purified by CD14+ MACS separation; (b) monocyte derived dendritic cells - cultured CD14+ monocytes with ovine IL-4 & GMCSF; (c) monocyte derived macrophages (MDM) - cultured adherent cells; (d) Chlamydia infected MDM.
Cattle: (a) CD14+ monocytes - purified by CD14+ MACS separation; (b) CD16hi++ monocytes - purified by CD16+ MACS separation, followed by flow cytometry to obtain the CD16hi++ monocytes (c) monocyte derived dendritic cells - cultured CD14+ monocytes with bovine IL-4 & GMCSF; (d) monocyte derived macrophages (MDM) - cultured adherent cells; (e) Chlamydia infected MDM.
Abstract
Myeloid subsets have distinct immunological functions. We had already phenotypically characterised unstimulated subsets in cattle and sheep. RNA-seq was conducted to provide additional and novel information. Although closely related, cattle and sheep differ in their susceptibility to a number of pathogens including Chlamydia abortus. We also investigated differences between cattle and sheep monocyte derived macrophages in their interaction with Chlamydia abortus.
Data Citation
Glass, E; Hope, J; Entrican, G; Corripio-Miyar, Y; Doull LE "2189N and 2190N Ruminant cattle myeloid cell subsets" Edinburgh DataVault DOI: 10.7488/775660a6-2d55-4416-979e-0d9e597787ea
Date made available | 2 Oct 2018 |
---|---|
Publisher | Edinburgh DataVault |
Date of data production | 2014 - 2015 |
Projects
- 2 Finished
-
Innate immunity and endemic diseases in livestock species
Collie, D., Beard, P., Bishop, S., Bronsvoort, M., Burt, D., Fitzgerald, R., Freeman, T., Gally, D., Gill, A., Glass, E., Hocking, P., Hope, J., Hume, D., Kaiser, P., Mabbott, N., McLachlan, G., Morrison, L., Stevens, J., Stevens, M. & Watson, M.
1/04/12 → 31/03/17
Project: Research
-
the route to identification of the immunological correlates of protection in ruminants
Glass, E., Hope, J. & Entrican, G.
1/02/12 → 31/07/15
Project: Research