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Objective: To characterize the differential and proliferative activities of FLK-1(+) cells derived from mouse fetal liver.
Method: The FLK-1(+) fraction were enriched from the fetal liver using immunomagnetic method and their differential and proliferative activities were examined in culture medium and in vivo via transplantation of FLK-1(+) cells into the inferior pole of the spleen of nine-week-old male C57 BL/6 mice after two-thirds hepatectomy.
Results: In response to growth factors, FLK-1(+) cells expressed typical lineage-specific markers for vascular endothelial cells, smooth muscle cells. Intrahepatic implantation of FLK-1(+) cells resulted in the formation of blood vessels in the fibrous capsule of partially hepatectomized liver.
Conclusion: These results indicate that FLK-1(+) cells derived from mouse fetal liver could differentiate into endothelial cells and smooth muscle cells and they may serve as potential stem cells for clinical cell-based therapy.
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Int J Oncol
November 2025
Department of Urology, The Fourth Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China.
Following the publication of the above paper, it was drawn to the Editor's attention by a concerned reader that, regarding the Transwell migration and invasion assay data shown in Fig. 3A and B, two pairs of panels appeared to contain overlapping sections of data (out of a total of ten panels), such that data which were intended to show the results from differently performed experiments appeared to have been derived from the same original sources. Upon analyzing the data independently in the Editorial Office, a third pair of data panels in the same figure were found to be similarly affected.
View Article and Find Full Text PDFBiochem Biophys Res Commun
September 2025
Suleyman Demirel University, Faculty of Pharmacy, Department of Basic Pharmaceutical Sciences, Isparta, 32260, Türkiye; Bahcesehir University, Faculty of Engineering and Natural Sciences, Istanbul, 34353, Türkiye. Electronic address:
In this study, benzimidazolium salts were designed and prepared in two steps. Synthesized compounds 3a and 3b were evaluated on human cancer cell lines (A549, HepG2, and MCF-7). IC values and selectivity indices were calculated.
View Article and Find Full Text PDFEur J Med Chem
November 2025
Department of Chemistry, College of Science, Engineering and Technology, University of South Africa, Private Bag X06, Florida, 1710, South Africa. Electronic address:
The development of small molecules capable of inhibiting multiple oncogenic pathways, such as those driven by the vascular endothelial growth factor receptor-2 (VEGFR-2) and epidermal growth factor receptor (EGFR) tyrosine kinases, represents a promising strategy in anticancer drug discovery. A strategically iodinated benzaldehyde precursor 1 was synthesized and condensed with phenylhydrazine derivatives to yield the iodophenol-hydrazones 2a and 2b. Subsequent Sonogashira coupling and cycloisomerization afforded novel benzofuran-hydrazone hybrids 3a-k with diverse aryl substituents.
View Article and Find Full Text PDFSci Rep
July 2025
Stem Cell Therapy Division, Institute of Science Tokyo, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8510, Japan.
The tumor microenvironment (TME) is deeply involved in cancer progression and treatment resistance. Although humanized mouse models have been developed by transplanting human cells into immunodeficient mice, they fail to fully reconstitute the TME. Blastocyst complementation using Flk-1 (Vegfr2, Kdr) knockout hosts offers a potential solution.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
August 2025
Vascular Biology and Molecular Pathology, Faculty and Graduate School of Dental Medicine, Hokkaido University, Sapporo 060-8586, Japan.
Aging is a risk factor for severe COVID-19, characterized by vascular endothelial dysfunction. Although possible susceptibility of vascular endothelial cells (ECs) to SARS-CoV-2 infection has been suggested, the details of entry into cells have not been clarified. Previously, we reported that in an aged mouse model of severe COVID-19, ECs show a massive viral uptake and inflammatory response.
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