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Label-free Chemical Characterization of Polarized Immune Cells in vitro and Host Response to Implanted Bio-instructive Polymers in vivo Using 3D OrbiSIMS.
Suvannapruk, Waraporn; Edney, Max K; Fisher, Leanne E; Luckett, Jeni C; Kim, Dong-Hyun; Scurr, David J; Ghaemmaghami, Amir M; Alexander, Morgan R.
Afiliación
  • Suvannapruk W; Advanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
  • Edney MK; Department of Chemical and Environmental Engineering, Faculty of Engineering, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
  • Fisher LE; Immunology & Immuno-bioengineering Group, School of Life Sciences, Faculty of Medicine and Health Sciences, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
  • Luckett JC; School of Life Sciences, Faculty of Medicine and Health Science, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
  • Kim DH; Advanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
  • Scurr DJ; Advanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
  • Ghaemmaghami AM; Immunology & Immuno-bioengineering Group, School of Life Sciences, Faculty of Medicine and Health Sciences, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
  • Alexander MR; Advanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
Bio Protoc ; 13(15): e4727, 2023 Aug 05.
Article en En | MEDLINE | ID: mdl-37575382
ABSTRACT
The Three-dimensional OrbiTrap Secondary Ion Mass Spectrometry (3D OrbiSIMS) is a secondary ion mass spectrometry instrument, a combination of a Time of Flight (ToF) instrument with an Orbitrap analyzer. The 3D OrbiSIMS technique is a powerful tool for metabolic profiling in biological samples. This can be achieved at subcellular spatial resolution, high sensitivity, and high mass-resolving power coupled with MS/MS analysis. Characterizing the metabolic signature of macrophage subsets within tissue sections offers great potential to understand the response of the human immune system to implanted biomaterials. Here, we describe a protocol for direct analysis of individual cells after in vitro differentiation of naïve monocytes into M1 and M2 phenotypes using cytokines. As a first step in vivo, we investigate explanted silicon catheter sections as a medical device in a rodent model of foreign body response. Protocols are presented to allow the host response to different immune instructive materials to be compared. The first demonstration of this capability illustrates the great potential of direct cell and tissue section analysis for in situ metabolite profiling to probe functional phenotypes using molecular signatures. Details of the in vitro cell approach, materials, sample preparation, and explant handling are presented, in addition to the data acquisition approaches and the data analysis pipelines required to achieve useful interpretation of these complex spectra. This method is useful for in situ characterization of both in vitro single cells and ex vivo tissue sections. This will aid the understanding of the immune response to medical implants by informing the design of immune-instructive biomaterials with positive interactions. It can also be used to investigate a broad range of other clinically relevant therapeutics and immune dysregulations. Graphical overview.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Bio Protoc Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Bio Protoc Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido
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