ArticleAnimals : an open access journal from MDPI2025
Development of Serum-Free Culture Systems for an Immortalized Porcine Kidney-Derived Macrophage Cell Line.
Article in Animals : an open access journal from MDPI, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Effects of low-serum adaptation on growth and protein expression in stably lactoferrin-overexpressing mammary alveolar cells.Frontiers in bioengineering and biotechnology · 2026Article
- A novel proliferation synergy factor cocktail maintains proliferation and improves transfection efficiency in muscle cells and fibroblasts under low-serum conditions.Frontiers in cell and developmental biology · 2025Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
The immortalized porcine kidney-derived macrophage (IPKM) cell line is an excellent resource that has proven to be an effective for the production of various strains of African swine fever virus (ASFV). In this study, we developed a serum-free medium to replace the standard serum-containing medium and established the long-term subculture of IPKM cells. We used KnockOut serum replacement instead of serum. As the expression of several cytokines and their receptors were observed in IPKM cells, we examined their effect and found that porcine colony stimulating factor 1 (pCSF1) and pCSF2 were essential for the proliferation of IPKM cells. Furthermore, the addition of 2% polyvinylpyrrolidone K90 to the medium improved cell adhesion and allowed for the stable long-term subculture of IPKM cells. The proportion of cells with a normal number of chromosomes (2n = 38) was similar to that of IPKM cells cultured in a serum-containing medium. Moreover, we investigated the spinner flask suspension culture without using microcarrier beads. Finally, we developed a modified serum- and calcium-free medium in which IPKM cells could be successfully cultured for an extended period. Whether grown in adherent or suspension culture, the expression of the macrophage-specific markers, CD172a, CD203a, and Iba1, remained positive, indicating that IPKM cells retained their macrophage properties.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.