Warning! You won't be able to use the quotation basket until you enable cookies in your Web browser.
Warning! Your Web browser is no longer supported. Please upgrade to a modern browser.

Techniques to Minimize Articular Cartilage Folding

Introduction

In my department we are not only interested in the histology of bone but also in studying the articular cartilage of joints. When we evaluate the articular cartilage, we are looking for any surface damage that has occurred from normal wear and tear or surgical models. After a joint has been decalcified the loss of proteoglycans in the articular cartilage causes it to fold and ripple during the staining process. When this occurs, it makes it impossible toperformhisto-morphometryor measurements of the cartilage. In this article, I will explain some helpful tips to reduce or eliminate folding of the articular cartilage.

Grossing/Fixation

Every step in the histology process is critical, from dissection up to and including cover-slipping, especially for articular cartilage samples. It is very important that your samples are dissected properly. For example, a mouse hind limb should be dissected well, leaving as little remaining soft and connective tissue as possible. When grossing around the joint, tissue is left intact to protect the joint (Figure 1). If samples are incorrectly grossed or not kept hydrated, they will neither decalcify nor process well leading to bad results. Bone samples should be fixed for a minimum of 72 hours in 10% Neutral Buffered Formalin. Samples are then rinsed well to remove the salts from fixation and then placed into a decalcifying agent, such as EDTA, for 7 to 14 days depending on the sample and its size. The decalcifying agent should be fresh and changed regularly. It is crucial to use a decalcification end point test, such as x-ray, chemical testing using ammonium oxalate (1) or weight test (2). It is imperative to remove all the calcium from the bone and equally important to not leave your samples in decalcification solution too long. Leaving samples in decalcifying agents too long causes excessive loss of the proteoglycans, increasing the odds of your sections folding.

Fig.1: Correctly grossed joint/tissue

Processing

Bone processing programs require longer processing cycles, generally 1 hour per station in automated processors. Larger samples such as rabbit and dog need longer programs. The Animal Processing Manual from the National Society for Histotechnology, Veterinary, Industry and Research Committee is a valuable reference for processing all types of tissue (3). We use xylene as a clearing agent as it gets water out of the bone tissue better than other clearing agents. We also use paraffin with higher concentrations of plastic polymers (Paraplast Plus) when processing, as it infiltrates bone tissue better. Tissue must be completely fixed before processing. A desired sample thickness is 3-4mm, or about the thickness of a penny. If a sample is too large and "stuffed" into a cassette, the reagents will not be able to dehydrate, clear or infiltrate the tissue.

Embedding

Paraffin embedding is a critical step in the histological process when working with bone and joint samples, as it is with any sample. The orientation of your sample is very important. If bone is embedded at an angle, it may cause the bone to break and “chunk out” of the block. Harder paraffin (Paraplast) makes sectioning bone easier; it allows more support and stability. Embed your tissue as flat as possible. If there is a cut side, embed that cut side down in the mold. We embed mouse leg, femur and tibia in a “smile” orientation with the tibia/fibula connection up, as we are focusing on the skeletal muscle (Figure 2).

Fig.2: Optimal embedding of mouse sample

Microtomy

Make sure you have a heavy duty microtome when cutting any type of bone sample. When trimming or facing into your block, be very careful! Trim slowly and change the blade when necessary. If you trim in too fast, you can cause the bone or joint to chunk out. Put your block on an ice tray with a thin layer of water and soak your block before cutting. The colder the block, the easier bone is to section. When a block is cold the paraffin is stronger, offering more support. When sectioning, if calcium still remains in your sample it may cause your sample to chunk out or the section to lift from the slide, increasing the chances of articular cartilage folding. Bone and joints are difficult to get to adhere to slides. Slide selection should be considered carefully; a slide that is more charged will decrease the odds of folding and rippling. Because bone can be tricky to embed, you must angle your chuck/block holder in order to get to the proper level or plane. Be patient!

Staining

When preparing your sections for routine or special staining, you must take special care to prevent articular cartilage folding. Generally, we bake our slides overnight at 60° C to remove paraffin as well as adhere tissue to the slides. However, we have found this is not the case with samples that have articular cartilage. In fact, after baking overnight the probability of folding increases greatly. We allow our sections to completely air dry overnight at room temperature. After drying, we place our slides horizontally on a slide dryer at 37° Celsius for a minimum of 12 hours. Many times we leave our slides on the slide dryer over the weekend. All of our staining is done manually, which allows us to handle our samples in the gentle manner they require. If you move too fast or jar the slides, it may cause bone and joints to fold and lift from the slide. We then run our slides through a series of xylene, 100% EtOH, 95% EtOH and 70% EtOH each for 5 minutes to dehydrate our samples. After we have dehydrated our samples, we leave them at room temperature for 30 minutes to completely dry before staining (Figure 3).In our experience, this is the key stepto reduce articular cartilage folding. After your section is completely dry, you can proceed to your stain protocol as normal. The other key factor to prevent articular cartilage folding is to air dry your sections again after a series of 70% EtOH, 95% EtOH and 100% EtOH for the rehydration step. After your slides are completely dry, dip them in xylene and coverslip.

The same steps used in the dehydration and rehydration processes can be used while performing immunohistochemistry to avoid articular cartilage folding.

Fig.3a: Decreased folding of cartilage when samples are air dried after dehydration prior to staining
Fig.3b: Increased folding of cartilage when samples are stained without using the air drying technique

Immunohistochemistry

Immunohistochemistry protocols that require heat induced antigen retrieval can be damaging to both the cartilage and bone. High temperatures can cause the bone and joint to lift off the slide completely or to ripple causing artifacts. If your immunohistochemistry protocol calls for using heat retrieval, lower the temperature and extend the incubation time.

When using histo-morphometry to measure articular cartilage following injury or surface damage, the articular cartilage cannot be folded. Folding of the cartilage will give measurements that are neither accurate nor true representations of your sample.

Careful and gentle handling of articular cartilage samples and sections is essential. Following proper histological steps from dissecting your tissue to cover slipping your slide are critical to obtaining quality articular cartilage sections.

References

  • Skinner RA, Hickmon SG, Lumpkin CK, Aronson J, Nicholas RW. Decalcified Bone: Twenty Years of Successful Specimen Management. The Journal of Histotechnology 1997;20;267-277.
  • Callis G, Sterchi D. Decalcification of Bone: Literature Review and Practical Study of Various Decalcifying Agents, Methods, and Their Effects on Bone Histology. The Journal of Histotechnology 1998;21;49-58.
  • Animal Processing Manual. First ed., National Society Of Histotechnology, 2002.

This presentation was prepared by Sarah Mack, Manager Histology at the University of Rochester, NY.

The presentation represents Sarah Mack’s views, and does not necessarily represent or reflect the views or opinions of Leica. It is for educational purposes only and is not intended as regulatory or legal advice or as diagnostic advice for a particular patient or a particular disease or condition.