Baby hamster kidney

In the procedure for the surface test (313), the vims is grown in a monolayer of baby hamster kidney cells and incubated in Eagles medium supplemented with tryptose phosphate broth and calf semm. After separation of the vims from the cells by sonification and centrifugation, amounts of the suspension containing 3 x 10 plaque-forrning units are dried on coversHps. The inoculated coversHps are placed in 5 ml of the disinfectant for 1, 5, or 10 min, then rinsed, sonicated, and assayed. 

Another application shows the preparative purification and polishing of a therapeutic fusion protein with a humanized recombinant IgG protein. The fusion protein was expressed by the fermentation of baby hamster kidney cells. The filtered culture supernatant (155 liters) contained 2.2 g of IgG and 75.5 g of total protein. After the immunoglobulins were isolated by expanded bed adsorption and rebuffering, the IgG fraction was bound to Fractogel EMD SOj (M). This column achieved baseline separation of complete antibodies (fusion protein) from small amounts of antibodies lacking the fusion part. The resulting highly purified IgG fraction (110 ml) was diluted to 150 ml and... 

For assaying herpes virus, monolayers of baby hamster kidney (BHK) cells are used. Virus titre is expressed as the number of plaque-forming units (pfu) per millilitre before and after exposure to a disinfectant, so that the virucidal efficacy of the test agent can be determined. A diagrammatic representation is given in Fig. 11.7. 

Kratje, R. B., Reimann, A., Hammer, J., and Wagner, R., Cultivation of Recombinant Baby Hamster Kidney Cells in a Fluidized Bed Bioreactor System with Porous Borosilicate Glass, Biotechnol. Prog., 10 410 (1994)... 

Many of the initial biopharmaceuticals approved were simple replacement proteins (e.g. blood factors and human insulin). The ability to alter the amino acid sequence of a protein logically coupled to an increased understanding of the relationship between protein structure and function (Chapters 2 and 3) has facilitated the more recent introduction of several engineered therapeutic proteins (Table 1.3). Thus far, the vast majority of approved recombinant proteins have been produced in the bacterium E. coli, the yeast S. cerevisiae or in animal cell lines (most notably Chinese hamster ovary (CHO) cells or baby hamster kidney (BHK) cells. These production systems are discussed in Chapter 5. 

In addition to fluorescence methods, another study [27] developed a method to permit electron microscopic localization of Ras anchor domains on cytoplasmic membrane surfaces by immunogold labeling. The particle neighbor distances can be analyzed to obtain information about possible domain structure. Expressing H-Ras and K-Ras in baby hamster kidney cells, a nonrandom particle distribution was obtained from which the estimated mean raft size was 7.5-22 nm and about 35% of the membrane area consists of rafts. The same technique applied to cells that had been incubated with [3-cydodextrin to reduce cholesterol produced completely random distributions of H-Ras. This cholesterol dependence suggests some type of coupling of rafts across the inner and outer membrane leaflets. 

Li+ has significant inhibitory effects upon DNA viruses, in particular HSV which has been studied in depth. It was originally shown that Li+ inhibits viral replication in a dose-dependent, reversible manner in HSV-infected baby hamster kidney cells [240], and this has been found to be due to a Li+-induced decrease in the synthesis of viral DNA [241]. It is now well established that Li+ inhibits DNA synthesis in HSV types 1 and 2 and in several other DNA viruses, including measles, vaccinia, adenovirus, poxvirus, pseudorabies virus, Epstein-Barr virus, and the bovine, equine, and canine HV s [241]. Interestingly, Li+ has no effect on the replication of RNA viruses, such as influenza or encephalomyo-carditis virus. 

M. C. Gehrmann, M. Opper, H. H. Sedlacek, K. Bosslet, J. Czech, Biochemical Properties of Recombinant Human /3-Glucuronidase Synthetized in Baby Hamster Kidney Cells , Biochem. J. 1994, 301, 821 - 828. 

Bacterial hosts are inappropriate choices for expression of proteins such as the blue copper proteins stellacyanin, laccase, and ceruloplasmin which are extensively glycosylated. In these cases, it may be necessary to employ tissue cultures of appropriate origin to obtain the native protein. In this regard, the amino-terminal half of human serum transferrin, which lacks carbohydrate, has been expressed in high yield in baby hamster kidney cells by Funk et al. [13], while the glycosylated carboxyl-terminus has proved to be more problematic [103]. 

Recently, it has been shown that cell-permeable cerantides dramatically inhibited the synthesis of the two major membrane phospholipids, PC and PE (Bladergroen et al, 1999b Allan, 2000). The inhibition of phospholipid synthesis was rapid, within 2 h, and resulted in massive apoptosis after 16-24 h. The mechanism by which short-chain cerantides exert their effect on phospholipid synthesis is possibly cell type dependent. In baby-hamster kidney (BHK) fibroblasts rc synthesis was reduced at the level of CT, the putative rate-determining enzyme in the CDP-choline pathway (Allan, 2000). This conclusion was based solely on radio-label studies in combination with an earlier published observation (Wieder et al, 1995) showing that C2-SM (the SM generated from C2-ceramide by SM synthase, which was actively synthesized in the BHK-cells) inhibited CT activity in vitro. On the other hand, data obtained from studies with rat-2 fibroblasts clearly showed that short-chain cerantides regulate the synthesis of PC and PE mainly at the final step of the CDP-pathways. This conclusion was based on the following observations (a) incorporation of [ H]-choline into PC and... 

The reader should be aware that other types of cells expressing CD 154 have been used to stimulate CLL cells. These include mouse fibroblast L-cells (NTL) (12, 20, 21, 23, 28) and baby hamster kidney cells (27). The CD 154 NIH3T3 cells used in this study were kindly provided by Dr. Eldering (Department of Pathology, Academic Medical Center, Amsterdam, The Netherlands). 

Table 3.8. Expression systems that are/could potentially be used for the production of recombinant biopharmaceutical products (CHO=Chinese hamster ovary BHK=baby hamster kidney)...

Table 3.9. Some biopharmaceuticals currently on the market that are produced by genetic engineering in either E. coli or animal cells. CHO = Chinese hamster ovary cells BHK = baby hamster kidney cells...

Technical advances facilitating genetic manipulation of animal cells now allow routine production of therapeutic proteins in such systems. The major advantage of these systems is their ability to carry out post-translational modification of the protein product. As a result, many biopharmaceuticals that are naturally glycosylated are now produced in animal cell lines (Table 3.9). Chinese hamster ovary (CHO) and baby hamster kidney (BHK) cells have become particularly popular in this regard. 

Chinese hamster ovary (CHO) cells and baby hamster kidney (BHK) cell lines have been most commonly used, in addition to other cell lines, such as various mouse carcinoma cell lines. The recombinant factor VIII product generally contains only VIILC (i.e. is devoid of vWF). However, both clinical and pre-clinical studies have shown that administration of this product to patients suffering from haemophilia A is equally as effective as administering blood-derived factor VIII complex. The recombinant VIILC product appears to bind plasma vWF with equal affinity to native VIILC, upon its injection into the patient s circulatory system. Animal and human pharmacokinetic data reveal no significant difference between the properties of recombinant and native products. 

Cell transformation, Syrian hamster embryo cells, clonal assay Cell transformation, baby hamster kidney BHK-21 cells... 

Danford, N. (1991) The genetie toxicology of or//zo-toluidine. Mutat. Res., 258, 207-236 Daniel, M.R. Dehnel, J.M. (1981) Cell transformation test with baby hamster kidney cells. In de Senes, F.J. Ashby, J., eds, Progress in Mutation Research, Volume 1, Evaluation of Short-Term Tests for Carcinogens. Report of the International Collaborative Program, Amsterdam, Elsevier Seienee, pp. 626-637... 

Fig. 2. Effect of serum concentration on the attachment and spreading of BHK-21 cells onto TCP2 surface. BHK-21 cells were seeded in media containing the indicated concentrations of intact serum (open squares), Fn-depleted serum (triangles). Vn-depleted serum (circles), or serum-free medium alone (the single closed square) and the attachment panel (A) and spreading panel (B) of the cells were determined after 90 min culture on TCP (panel (A, B)) Mean SEM. (Reproduced from J. Biomed. Mater. Res. [Ref. 11 Role of serum vitronection and fibronectin in adhesion of fibroblasts following seeding onto tissue culture polystyrene] through the courtesy of John Wiley Sons, Inc.) BHK-21 Fibroblast cell lines from Baby Hamster Kidney 2 Similar results on Primaria are also presented in [Ref 11]...

Baby hamster kidney cells were genetically modified to secrete high levels of human NGF before undergoing polymer encapsulation prior to implantation. Although the therapy showed potential for the treatment of neurological disorders, the emergence of stem cells offered far broader therapeutic scope. 

Abbreviations. Ab, antibody SC, subcutaneous IV, intravenous CHO HSA, human serum albumin SC, subcutaneous USP, United States Pharmacopeia AHF IU, international unit NMT, not more than Ig, immunoglobulin BHK, baby hamster kidney PEG, polyethylene glycol hGH, human growth hoimone IM, intramuscular WFI, water for injection. 

Yang, H.-Y., Lieska, N., Goldman, A., and Goldman, B. (1985). A 300,000 MW intermediate filament-associated protein in baby hamster kidney (BHK-21) cells. /. Biol. Chem. 100, 620-631. 

Menzel et al. [19] Glucose Ethanol Phosphate Saccharomyces cerevisiae, Acremonium chrysogenum and recombinant baby hamster kidney (rBHK) cell cultivations Co-immobilised glucose oxidase and peroxidase Co-immobilised alcohol oxidase and peroxidase Co-immobilised nucleoside phosphorylase, xanthin oxidase and peroxidase Potentiometric, fluoride sensitive (pF), buffer capacity insensitive electrolyte isolator semiconductor capacitor (pF-EIS-CAP) chip ... 

Butyrate appears to have its most profound effects on neoplastic cells such as HeLa in addition to morphological and biochemical differentiation, the fatty acid inhibits cell growth (2). Previous studies have established a correlation between decreased ganglioside synthesis and malignant transformation (43-46). Transformed baby hamster kidney and newborn rat kidney cells exhibited a loss of GM3 and sialyl transferase activity (43,44). 

The genetic manipulation of animal cells allows the production of therapeutic proteins in animal cell culture systems. Mammalian cells such as Chinese hamster ovarian cells and baby hamster kidney cells are commonly used. These mammalian hosts produce recombinant proteins that have almost identical properties to those made by human cells. However, the use of mammalian cells does have disadvantages. As noted earlier, they are expensive to use. This is influenced by their more complex nutritional requirements, their slower growth, and their increased susceptibility to physical damage (Walsh, 2003). 

The BHK-21 (baby hamster kidney) cell line consists of adherent fibroblasts, that can also be adapted to suspension culture, and was isolated from five 1-day-old hamsters (McPherson and Stoker, 1962). These cells are commonly used for virus propagation (polio, rabies, and foot-and-mouth disease) for production of veterinary vaccines. 

Schmid G, Zilg H, Eberhard U, Johannsen R (1991), Effect of free fatty acid and phospholipids on growth of and product formation by recombinant Baby Hamster Kidney (rBHK) and Chinese Hamster Ovary (rCHO) cells in culture, J. Biotechnol. 17 155-167. 

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