Slowly cycling (label‐retaining) epidermal cells behave like clonogenic stem cells in vitro
Abstract
Abstract. Slowly cycling label‐retaining epidermal cells were identified by light microscopic autoradiography in the dorsal epidermis and hair follicles of adult mice 8–10 weeks after twice daily injection of [3 H]dT on days three through five after birth. Pulse‐labelled epidermal cells were identified in the epidermis and hair follicles of 7–8 week old mice 1 h after a single injection of [3 H]dT at 8.00 a.m. For mice of both groups, epidermal cells including those from the hair follicles were harvested by trypsinization and were cultured from low density on feeder layers of irradiated Swiss mouse 3T3. On days 2, 4, 5, 7, 10 and 12, the cultures were fixed and processed for light microscopic autoradiography, and the distribution of labelled nuclei was quantified. On day 2 of culture, both label‐retaining cells (LRC) and pulse labelled cells (PLC) were found primarily as single cells. After five days, LRC were found as pairs and clusters having silver grain counts consistent with their division. In contrast, PLC remained primarily as single cells. These results suggest that LRC may divide to form colonies (are clonogenic) whereas PLC are rarely clonogenic. The significance of this experiment is that it suggests that the LRC may not only be persistent in the epidermis, but that they may also be cells with relatively greater proliferative potential than the PLC and are thus likely to be stem cells.
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SwGs are derived from an epidermal bud of CK5-expressing progenitors, sharing the same origin as epidermal keratinocytes.
“SwGs are derived from an epidermal bud of CK5‐expressing progenitors,[ 2 , 6 ] sharing the same origin as epidermal keratinocytes that can be readily maintained and propagated in vitro.[ 7 ]”
From Sweat Gland Organoids Originating from Reprogrammed Epidermal Keratinocytes Functionally Recapitulated Damaged Skin (2021) · cites this paper as [7]
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- Authors
- Morris, R. J., & Potten, C. S.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- Cancer Research UK Manchester Institute (GB)
- Corresponding author
- Morris, R. J.
- Venue
- Cell Proliferation
- Publisher
- Wiley
- Published
- 1994-05
- Volume
- 27
- Issue
- 5
- Pages
- 279-289
- ISSN
- 0960-7722 (ISSN-L)
- 1365-2184
- OpenAlex
- W2036949285
- Cited by
- 207
- References
- 1
- Citations by year
- 2023: 1 · 2022: 3 · 2021: 4 · 2020: 4 · 2019: 3 · 2018: 3 · 2017: 4 · 2016: 3 · 2015: 7 · 2014: 5 · 2013: 12 · 2012: 13
- FWCI
- 2.55
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell Proliferation (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (CA-45293)
- Topics
- Health Sciences › Medicine › Urology › Hair Growth and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Keywords
- label-retaining cells, epidermal stem cells, epidermal proliferation, clonogenicity, hair follicle, cell cycling, skin regeneration, cell colony formation
- MeSH terms
- Epidermal Cells, Aging, Animals, Animals, Newborn, Autoradiography, Cell Cycle, Cell Division, Cells, Cultured, Clone Cells, Female, Mice, Inbred Strains, Stem Cells, Time Factors, Keratinocytes, Hair Follicle, Mice
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