Magnetoresistive-based real-time cell phagocytosis monitoring

• Published in: Biosensors & bioelectronics Vol. 36; no. 1; pp. 116 - 122
• Main Authors: Shoshi, A., Schotter, J., Schroeder, P., Milnera, M., Ertl, P., Charwat, V., Purtscher, M., Heer, R., Eggeling, M., Reiss, G., Brueckl, H.
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier B.V 01.06.2012; Elsevier
• Subjects: Biological and medical sciences; Biosensing Techniques; Biotechnology; Cell Line; Fibroblasts - cytology; Fibroblasts - metabolism; Fundamental and applied biological sciences. Psychology; Humans; Magnetite Nanoparticles - chemistry; Microfluidic Analytical Techniques - methods; Phagocytosis - physiology; Real time; Monitoring; Phagocytosis
• ISSN: 0956-5663; 1873-4235
• DOI: 10.1016/j.bios.2012.04.002

The uptake of large particles by cells (phagocytosis) is an important factor in cell biology and also plays a major role in biomedical applications. So far, most methods for determining the phagocytic properties rely on cell-culture incubation and end-point detection schemes. Here, we present a lab-on-a-chip system for real-time monitoring of magnetic particle uptake by human fibroblast (NHDF) cells. It is based on recording the time evolution of the average position and distribution of magnetic particles during phagocytosis by giant-magnetoresistive (GMR) type sensors. We employ particles with a mean diameter of 1.2μm and characterize their phagocytosis-relevant properties. Our experiments at physiological conditions reveal a cellular uptake rate of 45 particles per hour and show that phagocytosis reaches saturation after an average uptake time of 27.7h. Moreover, reference phagocytosis experiments at 4°C are carried out to mimic environmental or disease related inhibition of the phagocytic behavior, and our measurements clearly show that we are able to distinguish between cell-membrane adherent and phagocytosed magnetic particles. Besides the demonstrated real-time monitoring of phagocytosis mechanisms, additional nano-biointerface studies can be realized, including on-chip cell adhesion/spreading as well as cell migration, attachment and detachment dynamics. This versatility shows the potential of our approach for providing a multifunctional platform for on-chip cell analysis. ► Real-time biochip-based magnetoresistive phagocytosis monitoring established. ► Relevant properties of magnetic particles with 1.2μm diameter well characterized. ► Human fibroblast (NHDF) cells phagocytose on average 45 particles per hour. ► Phagocytosis saturation is reached after about 28h. ► Studies at metabolically inhibited conditions show drastically reduced phagocytosis.