Dataset on gene expression profiling of multiple murine hair follicle populations

The murine hair follicle contains several different keratinocyte progenitor populations within its compartments. By using antibodies against CD34, Itgα6, Sca-1 and Plet-1, we have isolated eight populations and compared their Krt10 and Krt14 expressions using fluorescence microscopy. This improved p...

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Main Authors: Anders Patrik Gunnarsson, Rikke Christensen, Jian Li, Uffe Birk Jensen
Format: Article
Language:English
Published: Elsevier 2016-12-01
Series:Data in Brief
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340916305649
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spelling doaj-5fc07ab3203c4538adbf748f71f3f63c2020-11-25T01:32:03ZengElsevierData in Brief2352-34092016-12-019C32833410.1016/j.dib.2016.08.063Dataset on gene expression profiling of multiple murine hair follicle populationsAnders Patrik Gunnarsson0Rikke Christensen1Jian Li2Uffe Birk Jensen3Department of Clinical Genetics, Aarhus University Hospital, 8200 Aarhus, DenmarkDepartment of Clinical Genetics, Aarhus University Hospital, 8200 Aarhus, DenmarkThe Key Laboratory of Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, Nanjing, ChinaDepartment of Clinical Genetics, Aarhus University Hospital, 8200 Aarhus, DenmarkThe murine hair follicle contains several different keratinocyte progenitor populations within its compartments. By using antibodies against CD34, Itgα6, Sca-1 and Plet-1, we have isolated eight populations and compared their Krt10 and Krt14 expressions using fluorescence microscopy. This improved panel was used in our associated article doi:10.1016/j.scr.2016.06.002 (A.P. Gunnarsson, R. Christensen, J. Li, U.B. Jensen, 2016) [1] and the present dataset describes the basic controls for the FACS. We also used imaging flow cytometry to visualize the identified populations as control. A more detailed analysis of the global gene expression profiling is presented, focusing on the pilosebaceous unit. Murine whole-mounts were stained for heat shock protein Hspa2, which is exclusively expressed by keratinocytes with low or no expression of the four selection markers (IRK). Whole-mount labeling was also conducted to visualize Krt79 and Plet-1 coexpression within the hair follicle and quantification on the distribution of Krt79 positive keratinocytes is presented.http://www.sciencedirect.com/science/article/pii/S2352340916305649Epidermal keratinocytesStem cells
collection DOAJ
language English
format Article
sources DOAJ
author Anders Patrik Gunnarsson
Rikke Christensen
Jian Li
Uffe Birk Jensen
spellingShingle Anders Patrik Gunnarsson
Rikke Christensen
Jian Li
Uffe Birk Jensen
Dataset on gene expression profiling of multiple murine hair follicle populations
Data in Brief
Epidermal keratinocytes
Stem cells
author_facet Anders Patrik Gunnarsson
Rikke Christensen
Jian Li
Uffe Birk Jensen
author_sort Anders Patrik Gunnarsson
title Dataset on gene expression profiling of multiple murine hair follicle populations
title_short Dataset on gene expression profiling of multiple murine hair follicle populations
title_full Dataset on gene expression profiling of multiple murine hair follicle populations
title_fullStr Dataset on gene expression profiling of multiple murine hair follicle populations
title_full_unstemmed Dataset on gene expression profiling of multiple murine hair follicle populations
title_sort dataset on gene expression profiling of multiple murine hair follicle populations
publisher Elsevier
series Data in Brief
issn 2352-3409
publishDate 2016-12-01
description The murine hair follicle contains several different keratinocyte progenitor populations within its compartments. By using antibodies against CD34, Itgα6, Sca-1 and Plet-1, we have isolated eight populations and compared their Krt10 and Krt14 expressions using fluorescence microscopy. This improved panel was used in our associated article doi:10.1016/j.scr.2016.06.002 (A.P. Gunnarsson, R. Christensen, J. Li, U.B. Jensen, 2016) [1] and the present dataset describes the basic controls for the FACS. We also used imaging flow cytometry to visualize the identified populations as control. A more detailed analysis of the global gene expression profiling is presented, focusing on the pilosebaceous unit. Murine whole-mounts were stained for heat shock protein Hspa2, which is exclusively expressed by keratinocytes with low or no expression of the four selection markers (IRK). Whole-mount labeling was also conducted to visualize Krt79 and Plet-1 coexpression within the hair follicle and quantification on the distribution of Krt79 positive keratinocytes is presented.
topic Epidermal keratinocytes
Stem cells
url http://www.sciencedirect.com/science/article/pii/S2352340916305649
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