- Short Report
- Open Access
Amyloid-beta peptide degradation in cell cultures by mycoplasma contaminants
© Zhao et al; licensee BioMed Central Ltd. 2008
- Received: 29 February 2008
- Accepted: 30 June 2008
- Published: 30 June 2008
Cell cultures have become an indispensable tool in Alzheimer's disease research for studying amyloid-β (Aβ) metabolism. It is estimated that up to 35% of cell cultures in current use are infected with various mycoplasma species. In contrast with common bacterial and fungal infections, contaminations of cell cultures with mycoplasmas represent a challenging issue in terms of detectability and prevention. Mycoplasmas are the smallest and simplest self-replicating bacteria and the consequences of an infection for the host cells are variable, ranging from no apparent effect to induction of apoptosis.
Here we present evidence that mycoplasmas from a cell culture contamination are able to efficiently and rapidly degrade extracellular Aβ. As a result, we observed no accumulation of Aβ in the conditioned medium of mycoplasma-positive cells stably transfected with the amyloid-β precursor protein (APP). Importantly, eradication of the mycoplasma contaminant – identified as M. hyorhinis – by treatments with a quinolone-based antibiotic, restored extracellular Aβ accumulation in the APP-transfected cells.
These data show that mycoplasmas degrade Aβ and thus may represent a significant source of variability when comparing extracellular Aβ levels in different cell lines. On the basis of these results, we recommend assessment of mycoplasma contaminations prior to extracellular Aβ level measurements in cultured cells.
- Conditioned Medium
- Mycoplasma Contamination
- Mycoplasma Species
- Restriction Fragment Length Polymorphism Assay
- Mycoplasma Contaminant
Numerous primary and immortalized cell lines have been used to analyze APP processing and Aβ production in in vitro cultures. These cell culture systems have proven to be indispensable for the identification of pharmacological and genetic modifiers of APP metabolism prior to in vivo studies [6–8]. It is estimated that 15 to 35% of cell cultures in current use are infected with mycoplasmas . With a diameter of about 0.2 – 0.4 μm, mycoplasmas are small, slow-growing bacteria that are generally unaffected by the antibiotics used against common bacteria and fungi. They can go undetected for long periods of time as the contaminated cells may grow normally and appear normal by light microscopy. Mycoplasma contaminations can however have negative effects, ranging from inhibition of metabolism and growth to induction of malignant transformation or apoptosis [10, 11]. In this study, we show that mycoplasmas can degrade extracellular Aβ. These results indicate that mycoplasma contaminations can introduce an unsuspected source of variability in Aβ level measurements in cultured cells.
Characterization of extracellular Aβ produced by APP-transfected cells
The APP metabolites, sAPPα and Aβ, are readily detectable in the conditioned medium of HEK293 cells stably transfected with the human APP695 isoform (Figure 1B, first lane). As expected, treatment of these cells with the selective γ-secretase inhibitor, L-685,458, prevented Aβ production and promoted accumulation of the APP intermediate fragments C99 and C83 (Figure 1B, second lane).
Degradation of extracellular Aβ by mycoplasma contaminants
Mycoplasma contamination prevents Aβ accumulation in APP-transfected cells
Mycoplasma eradication restored Aβ accumulation in APP-transfected cells
Successful mycoplasma decontamination can be achieved by treatments with different antibiotics, including quinolones and tetracyclines . Contaminated APP-transfected cells were treated for one week with the quinolone-based antibiotic, MRA (4-oxo-quinolone-3-carboxylic acid derivative). The antibiotic treatment successfully eradicated the mycoplasmas (Figure 3A, lower panel), and restored Aβ accumulation in the conditioned medium of the APP-transfected cells (Figure 3A, middle panel). M. hyorhinis, M. orale, M. arginini, M. fermentans, M. hominis and Acholeplasma laidlawii represent 90–95% of the contaminants in mycoplasma-positive cells [12, 13]. By restriction fragment length polymorphism assay of PCR products amplified from a region of the conserved 16S rDNA gene in mycoplasma species , we determined that the APP-transfected cells were contaminated with the M. hyorhinis species (Figure 3B). Together these results show that mycoplasmas degrade Aβ in cell cultures.
Aβ peptides are degraded in cell culture systems and in vivo by at least four peptidases from the metallopeptidase family, neprilysin, endothelin-converting enzyme-1 and -2, and insulin-degrading enzyme . Bacteria express numerous proteases with important biological activities, such as degradation of tissue matrix proteins or activation of zymogens through limited proteolysis. The vast majority of the contaminations in mycoplasma-positive cells are due to M. hyorhinis, M. orale, M. arginini, M. fermentans, M. hominis and Acholeplasma laidlawii [12, 13]. Partial sequencing of the M. hominis genome predicted the expression of at least three metallopeptidases, and M. penetrans, a mycoplasma species isolated from human, is predicted to express oligopeptidase O1, a metallopeptidase from the M13 neprilysin family. Here M. hyorhinis was identified in the contaminated APP-transfected cell lines. It is conceivable that M. hyorhinis also expresses metallopeptidases with homologies with known mammalian metallopeptidases, which degrade Aβ but not large secreted proteins, such as sAPPα. Contamination with mycoplasmas would therefore provide a very efficient peptidase-driven mechanism of Aβ clearance.
In conclusion, we show that (i) mycoplasmas from cell culture contaminations degrade in vitro Aβ produced in cell lines, (ii) mycoplasma-positive APP-transfected cells do not accumulate Aβ in the conditioned medium, and (iii) eradication of the mycoplasma contaminant (i.e. M. hyorhinis) by treatments with a quinolone-based antibiotic, restored extracellular Aβ accumulation in APP-transfected cells. Together these results demonstrate that mycoplasmas may represent a significant source of variability when comparing extracellular Aβ levels between different cell lines. We therefore recommend assessment of mycoplasma contamination prior to extracellular Aβ level measurements in cultured cells.
We thank Dr. P. D. Mehta (Institute for Basic Research in Developmental Disabilities, Staten Island, NY) for generously providing us with R1 antibody. The authors are grateful to Dr. G. Agiostratidou (Albert Einstein College of Medicine, Bronx, NY) for assistance with the MycoSensor PCR Assay Kit.
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