The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Stimulation of Hepatic Lipocyte Collagen Production by Kupffer Cell–Derived Transforming Growth Factor β: Implication for A Pathogenetic Role in Alcoholic Liver Fibrogenesis
Abstract
Transforming growth factor β has a specific stimulatory effect on collagen formation by hepatic lipocytes, a cell type believed to be a major source of extracellular matrices in the liver. Because monocytes and macrophages are the known sources of transforming growth factor β, Kupffer cells–resident macrophages in the liver–may also play an important role in liver fibrogenesis by releasing this cytokine and stimulating lipocyte collagen production. The present study tested this hypothesis using Kupffer cells and hepatic lipocytes isolated from a rat model of alcoholic liver fibrosis. Kupffer–cell–conditioned medium derived from the rat liver with alcoholic fibrosis, but not that from pair–fed control animals, significantly stimulated the net collagen formation of lipocytes isolated from the alcohol–fed, pair–fed control and chow–fed animals. Acidification of the Kupffer–cell–conditionied medium potentiated this effect threefold to fourfold, indicating the presence of a latent form. Fractionation of the Kupffer–cell–conditioned medium by high–performance liquid chromatography gel filtration revealed the major peak of the stimulatory activity corresponding to the molecular weight between 20 kD and 30 kD. It was completely inhibited by anittransforming growth factor β IgG. Furthermore, Northern blotting and hybridization of Kupffer–cell messenger RNA from alcohol–fed rats with 32 P–labeled transforming growth factor β complementary DNA demonstrated the presence of 2.5 kb messenger RNA for this cytokine. We conclude that: (a) Kupffer cells isolated from the rat liver with alcoholic fibrosis express and release transforming growth factor β; (b) that this cytokine is largely responsible for the Kupffer–cell–conditioned medium–induced stimulation of collagen formation by hepatic lipocytes; and (c) that this may represent a possible molecular mechanism of lipocyte stimulation during alcoholic liver fibrogenesis.(HEPATOLOGY 1990; 11:599:605.)
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
An endotoxin-induced serum factor that causes necrosis of tumors
Carswell, E. A., Old, L. J., Kassel, R. L., Green, S., Fiore, N., & Williamson, B. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.9.3666 · Cited by 4,532
Ignotz, R. A., & Massagué, J. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)35666-1 · Cited by 2,492
Cited by
Hepatic Stellate Cells: Protean, Multifunctional, and Enigmatic Cells of the Liver
Friedman, S. L. (2008) · Physiological Reviews · doi:10.1152/physrev.00013.2007 · Cited by 2,842
Liver fibrosis – from bench to bedside
Friedman, S. L. (2003) · Journal of Hepatology · doi:10.1016/s0168-8278(02)00429-4 · Cited by 1,780
Liver Fibrosis: Mechanistic Concepts and Therapeutic Perspectives
Roehlen, N., Crouchet, E., & Baumert, T. F. (2020) · Cells · doi:10.3390/cells9040875 · Cited by 1,237
Models of liver fibrosis: exploring the dynamic nature of inflammation and repair in a solid organ
Iredale, J. P. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30542 · Cited by 866
Role of Kupffer cells in the pathogenesis of liver disease
Kolios, G. (2006) · World Journal of Gastroenterology · doi:10.3748/wjg.v12.i46.7413 · Cited by 505
Metadata
- Authors
- Matsuoka, M., & Tsukamoto, H.
- Venue
- Hepatology
- Published
- 1990-04
- Volume
- 11
- Issue
- 4
- Pages
- 599-605
- ISSN
- 0270-9139 (ISSN-L)
- OpenAlex
- W2062460706
- Cited by
- 291
- References
- 2
- FWCI
- 10.18
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Stimulation of Hepatic Lipocyte Collagen Production by Kupffer Cell–Derived Transforming Growth Factor β: Implication for A Pathogenetic Role in Alcoholic Liver Fibrogenesis. https://app.cochat.ai/papers/10.1002/hep.1840110412
- The paper
- Matsuoka, M., & Tsukamoto, H. (1990). Stimulation of Hepatic Lipocyte Collagen Production by Kupffer Cell–Derived Transforming Growth Factor β: Implication for A Pathogenetic Role in Alcoholic Liver Fibrogenesis. Hepatology. https://doi.org/10.1002/hep.1840110412
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.