Immunohistochemical analysis of development of desmin‐positive hepatic stellate cells in mouse liver
Open accessAbstract
Development of desmin‐positive hepatic stellate cells was studied in mice using double immunofluorescent techniques and in vitro cultures with special attention given to their cell lineages. Several studies recently reported on the presence of cells that are immunologically reactive with both antidesmin and anticytokeratin antibodies in young fetal rat livers, and suggested the possibility that these cells give rise to hepatocytes and hepatic stellate cells. At early stages of mouse liver development, stellate cells with desmin‐positive filaments were scattered in the liver parenchyma. However, the stellate cells definitely differed from hepatoblasts and hepatocytes in terms of their morphology and expression of desmin and hepatoblast and hepatocyte‐specific E‐cadherin in the liver. Fetal hepatoblasts and hepatocytes did not react with antidesmin antibodies, nor did desmin‐positive stellate cells express E‐cadherin in vivo and in vitro. Thus it is likely that desmin‐positive stellate cells and hepatoblasts belong to different cell lineages. In the fetal liver, the desmin‐positive stellate cells surrounded blood vessels, and extended their processes to haematopoietic cells and megakaryocytes. Many, but not all, hepatoblasts and hepatocytes were observed to be associated with the stellate cells. At fetal stages, cellular processes positive for desmin in the stellate cells were also thick compared with those in the adult liver, in which desmin‐positive stellate cells lay in Disse's space and were closely associated with all hepatocytes. These developmental changes in the geography of desmin‐positive cells in the liver parenchyma and their morphology may be associated with their maturation and interactions with other cell types.
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The majority (87%) of p16+ senescent cells stained positive for desmin, indicating they were derived from HSCs.
“The majority (87%) of p16+ senescent cells stained positive for desmin, a marker for HSCs (27), indicating that they were derived from HSCs”
From Senescent hepatic stellate cells promote liver regeneration through IL-6 and ligands of CXCR2 (2022) · cites this paper as [27]
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- Authors
- NITOU, M., ISHIKAWA, K., & SHIOJIRI, N.
- Affiliations
- Shizuoka University (JP)
- Corresponding author
- SHIOJIRI, NOBUYOSHI
- ORCID
- SHIOJIRI, NOBUYOSHI
- Venue
- Journal of Anatomy
- Publisher
- Wiley
- Published
- 2000-11
- Volume
- 197
- Issue
- 4
- Pages
- 635-646
- ISSN
- 0021-8782 (ISSN-L)
- 1469-7580
- OpenAlex
- W2091986760
- Cited by
- 46
- References
- 51
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 1 · 2021: 4 · 2020: 5 · 2018: 1 · 2017: 4 · 2016: 1 · 2015: 1 · 2014: 1 · 2013: 1 · 2012: 3
- FWCI
- 0.73
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Anatomy (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Shizuoka University
- Japan Science Society
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Surgery › Organ Transplantation Techniques and Outcomes
- Keywords
- hepatic stellate cells, desmin, liver development, fetal liver, hepatoblasts, hepatocytes, E-cadherin, cell lineage, Disse's space
- MeSH terms
- Albumins, alpha-Fetoproteins, Animals, Carbamoyl-Phosphate Synthase (Ammonia), Desmin, Immunohistochemistry, Keratins, Liver, Mice, Inbred C3H, Immunoblotting, Cadherins, Cell Culture Techniques, Cell Lineage, Hepatocytes, Mice
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