Analysing the depletion of microglia and myeloid cells in the cd11b-dtr/cd45-dtr mice.

Predecessor experiments have shown that microglia and myeloid cells are depleted in cd45-dtr homozygous mice but we wanted to test if cd11b-dtr/cd45-dtr heterozygous mice are able to deplete these cells just as efficiently. We generated transgenic cd11b-dtr/cd45-dtr heterozygous mice and administere...

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Bibliographic Details
Main Author: Tan, Kah Sheng.
Other Authors: Klaus Erik Karjalainen
Format: Final Year Project (FYP)
Language:English
Published: 2013
Subjects:
Online Access:http://hdl.handle.net/10356/52456
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author Tan, Kah Sheng.
author2 Klaus Erik Karjalainen
author_facet Klaus Erik Karjalainen
Tan, Kah Sheng.
author_sort Tan, Kah Sheng.
collection NTU
description Predecessor experiments have shown that microglia and myeloid cells are depleted in cd45-dtr homozygous mice but we wanted to test if cd11b-dtr/cd45-dtr heterozygous mice are able to deplete these cells just as efficiently. We generated transgenic cd11b-dtr/cd45-dtr heterozygous mice and administered different concentrations of diphtheria toxin to analyse the depletion profile of both types of mice. After which the spleen and bone marrow were analysed for myeloid cell populations via fluorescence-activated cell sorting (FACS) and cell counting under a light-field microscope. The brains were analysed for microglia via FACS. A blood analysis was carried out using a haematology analyser machine. It was found that cd11b-dtr/cd45-dtr heterozygous mice are able to deplete microglial cells (in the brain) and myeloid cells (in the spleen and bone marrow, and blood) but the depletion was not as efficient as that observed in the cd45-dtr homozygous mice.
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spelling ntu-10356/524562023-02-28T18:04:40Z Analysing the depletion of microglia and myeloid cells in the cd11b-dtr/cd45-dtr mice. Tan, Kah Sheng. Klaus Erik Karjalainen School of Biological Sciences DRNTU::Science::Biological sciences::Microbiology::Immunology Predecessor experiments have shown that microglia and myeloid cells are depleted in cd45-dtr homozygous mice but we wanted to test if cd11b-dtr/cd45-dtr heterozygous mice are able to deplete these cells just as efficiently. We generated transgenic cd11b-dtr/cd45-dtr heterozygous mice and administered different concentrations of diphtheria toxin to analyse the depletion profile of both types of mice. After which the spleen and bone marrow were analysed for myeloid cell populations via fluorescence-activated cell sorting (FACS) and cell counting under a light-field microscope. The brains were analysed for microglia via FACS. A blood analysis was carried out using a haematology analyser machine. It was found that cd11b-dtr/cd45-dtr heterozygous mice are able to deplete microglial cells (in the brain) and myeloid cells (in the spleen and bone marrow, and blood) but the depletion was not as efficient as that observed in the cd45-dtr homozygous mice. Bachelor of Science in Biological Sciences 2013-05-09T03:32:18Z 2013-05-09T03:32:18Z 2013 2013 Final Year Project (FYP) http://hdl.handle.net/10356/52456 en Nanyang Technological University 34 p. application/pdf
spellingShingle DRNTU::Science::Biological sciences::Microbiology::Immunology
Tan, Kah Sheng.
Analysing the depletion of microglia and myeloid cells in the cd11b-dtr/cd45-dtr mice.
title Analysing the depletion of microglia and myeloid cells in the cd11b-dtr/cd45-dtr mice.
title_full Analysing the depletion of microglia and myeloid cells in the cd11b-dtr/cd45-dtr mice.
title_fullStr Analysing the depletion of microglia and myeloid cells in the cd11b-dtr/cd45-dtr mice.
title_full_unstemmed Analysing the depletion of microglia and myeloid cells in the cd11b-dtr/cd45-dtr mice.
title_short Analysing the depletion of microglia and myeloid cells in the cd11b-dtr/cd45-dtr mice.
title_sort analysing the depletion of microglia and myeloid cells in the cd11b dtr cd45 dtr mice
topic DRNTU::Science::Biological sciences::Microbiology::Immunology
url http://hdl.handle.net/10356/52456
work_keys_str_mv AT tankahsheng analysingthedepletionofmicrogliaandmyeloidcellsinthecd11bdtrcd45dtrmice