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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

We present a step-by-step approach to identify and address the most common problems associated with atomic force microscopy micro-indentations. We exemplify the emerging problems on native human articular cartilage explants characterized by various degrees of osteoarthritis-driven degeneration.

Abstract

Without a doubt, atomic force microscopy (AFM) is currently one of the most powerful and useful techniques to assess micro and even nano-cues in the biological field. However, as with any other microscopic approach, methodological challenges can arise. In particular, the characteristics of the sample, sample preparation, type of instrument, and indentation probe can lead to unwanted artifacts. In this protocol, we exemplify these emerging issues on healthy as well as osteoarthritic articular cartilage explants. To this end, we first show via a step-by-step approach how to generate, grade, and visually classify ex vivo articular cartilage discs according to different stages of degeneration by means of large 2D mosaic fluorescence imaging of the whole tissue explants. The major strength of the ex vivo model is that it comprises aged, native, human cartilage that allows the investigation of osteoarthritis-related changes from early onset to progression. In addition, common pitfalls in tissue preparation, as well as the actual AFM procedure together with the subsequent data analysis, are also presented. We show how basic but crucial steps such as sample preparation and processing, topographic sample characteristics caused by advanced degeneration, and sample-tip interaction can impact data acquisition. We also subject to scrutiny the most common problems in AFM and describe, where possible, how to overcome them. Knowledge of these limitations is of the utmost importance for correct data acquisition, interpretation, and, ultimately, the embedding of findings into a broad scientific context.

Introduction

Due to the ever-shrinking size of electronic devices and systems, the rapid development of micro- and nano-based technology and equipment has gained momentum. One such device is atomic force microscopy (AFM), which can scan biological surfaces and retrieve topographic or biomechanical information at both nano- and micrometer scales1,2. Among its vast features, this tool can be operated as a micro- as well as a nano-indenter to obtain information about the mechanical properties of various biological systems3,4,5,<....

Protocol

Femoral condyles collected from patients undergoing total knee arthroplasty at the University Hospital of Tübingen, Germany, were used. Only articular cartilage samples from patients with degenerative and posttraumatic joint pathologies were included in this study. Departmental, institutional, as well as local ethical committee approval were obtained before the commencement of the study (Project no.674/2016BO2). Written informed consent was received from all patients before participation.

NOTE: A flowchart of the experiment steps in their chronological order is given in Figure 1.

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Representative Results

Using a self-made cutting device, we were able to explant and generate small (4 mm x 1 mm) cartilage discs from fresh human condyles containing a single cellular spatial pattern30 of single strings (SS, Figure 2A), double strings (DS), small clusters (SC), big clusters (BC; Figure 2A), and diffuse (Figure 2B). A representative cartilage explant is depicted in Figure 3A. The .......

Discussion

As a progressive and multifactorial disease, OA triggers structural and functional changes in the articular cartilage.Throughout the course of OA, impairments in mechanical features are accompanied by structural and biochemical changes at the surface of the articular cartilage27,31. The earliest pathological events occurring in OA are proteoglycan depletion coupled with collagen network disruption32,33

Disclosures

The authors have nothing to disclose.

Acknowledgements

We thank the orthopedic surgeons from the Department of Orthopaedic Surgery of the University Hospital of Tuebingen for providing the tissue samples.

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Materials

NameCompanyCatalog NumberComments
Amphotericin BMerck KGaA, Darmstadt, Germany1397-89-3
Atomic force microscop (AFM) head CellHesion 200, Bruker Nano GmbH, Berlin, GermanyJPK00518
Biocompatible sample glue Bruker Nano GmbH, Berlin, GermanyH000033
Calcein AMCayman, Ann Arbor, Michigan, USA14948Cell membrane permeable stain, used for cartilage disc sorting- top view imaging
CantileverBruker Nano GmbH, Berlin, GermanySAA-SPH-5UMFrequency Nom: 30KHz, k: 0.2N/m, lenght nom: 115μm, width nom: 40μm,  geometry: rectangular, cylindrical tip with a 5μm end radius
Cartilage ctting device Self-made n/aCutting plastic device containing predefined wholes of 4mmx1mm
CDD camera integrated in the AFMThe Imaging Source Europe GmbH, Bremen, GermanyDFK 31BF03
CDD camera integrated in the fluorescence microscopeLeica Biosystems, Wetzlar, GermanyDFC3000G
CryotomeLeica Biosystems, Wetzlar, GermanyCM3050S 
Data Processing Software for the AFMBruker Nano GmbH, Berlin, Germanyn/aVersion 5.0.86,  can be downloaded for free from the following website https://customers.jpk.com
Dulbecco's modified Eagle's medium (DMEM) Gibco, Life Technologies, Darmstadt, Germany41966052
Fluorescence Microscope (Leica DMi8)Leica Biosystems, Wetzlar, Germany11889113
Glass block cantiliver holderBruker Nano GmbH, Berlin, GermanySP-90-05Extra long glass block with angled faces, designed especially for the use with the JPK PetriDishHeaterTM (Bruker).
Inverted phase contrast microscope (integrated in the AFM)AxioObserver D1, Carl Zeiss Microscopy, Jena, GermanyL201306_03
Leibovitz's L-15 medium without L-glutamine Merck KGaA, Darmstadt, GermanyF1315
Microscope glass slidesSigma-Aldrich, St. Louis, Missouri, USACLS294775X50
Mounting medium With DAPIibidi GmbH, Gräfelfing, Germany50011Mounting media with nuclear DAPI (4′,6-diamidino-2-phenylindole) counterstaining used for cartilage discs  side view imaging
Penicillin-StreptomycinSigma-Aldrich, St. Louis, Missouri, USAP4333
Petri dish heater associated with AFM (Petri Dish Heater)Bruker Nano GmbH, Berlin, GermanyT-05-0117
ScalpelFeather Medical Products, Osaka, Japan2023-01
Silicone SkirtBruker Nano GmbH, Berlin, Germanyn/aProtective silicone membrane (D55x0.25) which is placed on the basis of the base of the glas block to prevent  medium condensation in the AFM head.
Statistical program - SPSSIBM, Armonk, New York, USASPSS Statistics 22Vesion 280.0.0.0 (190)
Tissue culture dishes TPP Techno Plastic Products AG, Trasadingen, SwitzerlandTPP93040
Tissue-tek O.C.T. CompoundSakura Finetek, Alphen aan den Rijn, NetherlandsSA6255012Water-soluble embedding medium 

References

  1. Allison, D. P., Mortensen, N. P., Sullivan, C. J., Doktycz, M. J. Atomic force microscopy of biological samples. Wiley Interdisciplinary Reviews. Nanomedicine and Nanobiotechnology. 2 (6), 618-634 (2010).
  2. Deng, X., et al. Application of atomic force....

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Articular CartilageOsteoarthritisMicro indentationAtomic Force MicroscopyCartilage ExplantsBiomechanical PropertiesIn Vitro ModelCartilage DiscFluorescence MicroscopyAFM Calibration

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