2010
DOI: 10.1177/193229681000400506
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Importance of Interleukin-1 and Interleukin-1 Receptor Antagonist in Short-Term Glucose Sensor Function in Vivo

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Cited by 11 publications
(14 citation statements)
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“…Glucose sensors were implanted into IL-1Ra~KO, IL-1Ra~OE, or C57BL/6j mice, and CGM was undertaken for a period up to 28 days as described previously. [12][13][14] Blood glucose reference measurements were obtained periodically over the 28-day implantation period, using blood obtained from the tail vein and a FreeStyle blood glucose monitor. The Institutional Animal Care and Use Committee of the University of Connecticut Health Center (Farmington, CT) approved all mice studies.…”
Section: Glucose Sensors Implantation and Murine Continuous Glucosementioning
confidence: 99%
“…Glucose sensors were implanted into IL-1Ra~KO, IL-1Ra~OE, or C57BL/6j mice, and CGM was undertaken for a period up to 28 days as described previously. [12][13][14] Blood glucose reference measurements were obtained periodically over the 28-day implantation period, using blood obtained from the tail vein and a FreeStyle blood glucose monitor. The Institutional Animal Care and Use Committee of the University of Connecticut Health Center (Farmington, CT) approved all mice studies.…”
Section: Glucose Sensors Implantation and Murine Continuous Glucosementioning
confidence: 99%
“…CC chemokines or Beta-chemokines have two (2) adjacent cysteines near the amino terminus of the CC chemokine. CCL2 or monocyte chemotactic protein-1 (MCP-1) is an extremely powerful monocyte chemotactic factor that recruits monocytes from the vasculature into injured tissue and upon activation transforms them into macrophages (Semple et al 2010b; Semple et al 2010c). Chemokine receptors, such as CCR2, are G protein-coupled receptors that are expressed on the surface of leukocytes.…”
Section: Introductionmentioning
confidence: 99%
“…11 Because it will be essential to avoid any biological responses that may interfere with detection of glucose, the sensor should not elicit any significant inflammatory response following implantation in vivo. [12][13][14][15] Hence, the purpose of these in vitro studies was not to accurately predict sensor performance in vivo, 16 but to enable a preliminary screen of biocompatibility in order to remove materials that would otherwise elicit a detrimental immunological response inside the body. 5 Polymorphonuclear leukocytes (PMN) can be activated by invading pathogens as a favorable event to combat infection as well as by artificial materials, then often with unfavorable effects damaging the surrounding tissue with impairment of the device function.…”
Section: Introductionmentioning
confidence: 99%