The human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice.

The 5' region of the human lysozyme gene from -3500 to +25 was fused to a chloramphenicol acetyltransferase (CAT) reporter gene and three transgenic founder mice were obtained. All three transgenic lines showed the same pattern of CAT enzyme expression in adult mouse tissues that was consistent...

Full description

Bibliographic Details
Main Authors: Clarke, S, Greaves, D, Chung, L, Tree, P, Gordon, S
Format: Journal article
Language:English
Published: 1996
_version_ 1797071304211300352
author Clarke, S
Greaves, D
Chung, L
Tree, P
Gordon, S
author_facet Clarke, S
Greaves, D
Chung, L
Tree, P
Gordon, S
author_sort Clarke, S
collection OXFORD
description The 5' region of the human lysozyme gene from -3500 to +25 was fused to a chloramphenicol acetyltransferase (CAT) reporter gene and three transgenic founder mice were obtained. All three transgenic lines showed the same pattern of CAT enzyme expression in adult mouse tissues that was consistent with the targeting of elicited, activated macrophages in tissues and developing and elicited granulocytes. In normal mice high CAT enzyme activity was found in the spleen, lung, and thymus, tissues rich in phagocytically active cells, but not in many other tissues, such as the gut and muscle, which contain resident macrophages. Cultured resident peritoneal macrophages and cells elicited 18 hr (granulocytes) and 4 days (macrophages) after injection of sterile thioglycollate broth expressed CAT activity. Bacillus Calmette-Guérin infection of transgenic mice resulted in CAT enzyme expression in the liver, which contained macrophage-rich granulomas, whereas the liver of uninfected mice did not have any detectable CAT enzyme activity. Although the Paneth cells of the small intestine in both human and mouse produce lysozyme, the CAT gene, under the control of the human lysozyme promoter, was not expressed in the mouse small intestine. These results indicate that the human lysozyme promoter region may be used to direct expression of genes to activated mouse myeloid cells.
first_indexed 2024-03-06T22:51:20Z
format Journal article
id oxford-uuid:5ee1eca5-426b-4daf-8fc3-582e9a220774
institution University of Oxford
language English
last_indexed 2024-03-06T22:51:20Z
publishDate 1996
record_format dspace
spelling oxford-uuid:5ee1eca5-426b-4daf-8fc3-582e9a2207742022-03-26T17:43:29ZThe human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5ee1eca5-426b-4daf-8fc3-582e9a220774EnglishSymplectic Elements at Oxford1996Clarke, SGreaves, DChung, LTree, PGordon, SThe 5' region of the human lysozyme gene from -3500 to +25 was fused to a chloramphenicol acetyltransferase (CAT) reporter gene and three transgenic founder mice were obtained. All three transgenic lines showed the same pattern of CAT enzyme expression in adult mouse tissues that was consistent with the targeting of elicited, activated macrophages in tissues and developing and elicited granulocytes. In normal mice high CAT enzyme activity was found in the spleen, lung, and thymus, tissues rich in phagocytically active cells, but not in many other tissues, such as the gut and muscle, which contain resident macrophages. Cultured resident peritoneal macrophages and cells elicited 18 hr (granulocytes) and 4 days (macrophages) after injection of sterile thioglycollate broth expressed CAT activity. Bacillus Calmette-Guérin infection of transgenic mice resulted in CAT enzyme expression in the liver, which contained macrophage-rich granulomas, whereas the liver of uninfected mice did not have any detectable CAT enzyme activity. Although the Paneth cells of the small intestine in both human and mouse produce lysozyme, the CAT gene, under the control of the human lysozyme promoter, was not expressed in the mouse small intestine. These results indicate that the human lysozyme promoter region may be used to direct expression of genes to activated mouse myeloid cells.
spellingShingle Clarke, S
Greaves, D
Chung, L
Tree, P
Gordon, S
The human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice.
title The human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice.
title_full The human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice.
title_fullStr The human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice.
title_full_unstemmed The human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice.
title_short The human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice.
title_sort human lysozyme promoter directs reporter gene expression to activated myelomonocytic cells in transgenic mice
work_keys_str_mv AT clarkes thehumanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT greavesd thehumanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT chungl thehumanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT treep thehumanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT gordons thehumanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT clarkes humanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT greavesd humanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT chungl humanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT treep humanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice
AT gordons humanlysozymepromoterdirectsreportergeneexpressiontoactivatedmyelomonocyticcellsintransgenicmice