Do's and Don'ts in the Preparation of Muscle Cryosections for Histological Analysis

Podsumowanie

Here we demonstrate the most efficient methods for freezing, embedding, cryosectioning, and staining of muscle biopsies to avoid freezing artifacts.

Streszczenie

Histological evaluation of muscle biopsies has served as an indispensable tool in the understanding of the development and progression of pathology of neuromuscular disorders. However, in order to do so, proper care needs to be taken when excising and preserving tissues to achieve optimal staining. One method of tissue preservation involves fixing tissues in formaldehyde and then embedding them with paraffin wax. This method preserves morphology well and allows for long-term storage at RT but is cumbersome and requires handling of toxic chemicals. Further, formaldehyde fixation results in antigen cross-linking, which necessitates antigen retrieval protocols for effective immunostaining. On the contrary, frozen sectioning does not require fixation and thus retains biological antigen conformation. This method also provides a distinct advantage in quick turn around time, making it especially useful in situations needing quick histological evaluation like intraoperative surgical biopsies. Here we describe the most effective method of preparing muscle biopsies for visualization with different histological and immunological stains.

Wprowadzenie

Examination of muscle histology plays a critical role in the understanding of different types of neuromuscular disorders^1-4. When combined with other techniques, it allows researchers to get a better idea of the manifestation and progression of pathology and can also be essential to evaluate the efficacy of a therapeutic intervention^5-10. However, to be accurate, the tissues need to be preserved in the proper manner so as to preserve the physiological state immediately before excision. This requires great care during removal, preservation, sectioning, and staining.

Tissues can be prepared in two different ways for light microscopic study. The first method, formalin fixed paraffin embedded (FFPE) sections, requires tissues to be fixed in 10% natural buffered formaldehyde before being embedded with paraffin wax^11,12. The fixation step helps to preserve morphology better but also cross links endogenous proteins thus necessitating intricate antigen retrieval procedures for immunostaining and eliminating the possibility of enzymatic staining on such sections¹². Frozen sections, on the other hand, do not need to be pre-fixed or processed; therefore, proteins are able to retain native biological conformations^13,14. Further, frozen sections also allow for quick turnaround time, which at times is necessary, for example in the intraoperative diagnosis of sarcomas and other surgical biopsies¹⁵. However, if not done properly, this method is prone to freeze damage, which introduces changes to muscle architecture making the sections unfit for histological examination. This paper will outline the most effective method to prepare muscle biopsies in order to achieve optimal staining for proper examination.

Protokół

1. Tissue Harvest and Freezing of Muscle Tissues

1. Euthanize the mouse with an overdose of isoflurane (2-chloro-2-(difluoromethoxy)-1,1,1-trifluoro-ethane). Perform this step in a fume hood and use a secondary containment method such as a desiccator or a bell jar containing a cotton swab soaked in isoflurane.
2. Confirm death by firmly squeezing footpad. Use a secondary method of euthanasia such as cervical dislocation.
3. Wet the fur with 70% alcohol to reduce the sticking of loose hair strands on the muscles. Peel the skin off the limb using a fine forceps such as #5.
4. Carefully separate the muscle of interest (tibialis anterior (TA) in this case) from the bones underneath, starting from the tendon and remove.
5. Excise the muscle, cover it in OCT (Optimum Cutting Temperature compound), and lay it flat on a labeled disposable freezing mold. Make sure that the muscle is at its normal physiological orientation (head to tail) without stretching. Alternatively, freeze the muscle on small styrofoam squares and pin it using insect pins to ensure the correct length of the muscles.
6. Chill 2-methylbutane (isopentane) in a steel beaker using liquid nitrogen. This takes on average 3 - 5 min. Keep stirring intermittently until white precipitates start to form on the bottom and walls of the beaker.
   NOTE: When this occurs, isopentane has reached optimal freezing temperature (-150 °C)
7. Dip the molds containing muscles in the chilled 2-methylbutane. Freeze small muscles such as the diaphragm and extensor digitorum longus (EDL) for 6 - 12 sec and larger muscles like the gastrocnemius soleus (GS) and triceps for 15 - 20 sec. Do not freeze the muscles for too long as this may lead to cracking.
8. Transfer the frozen tissues on to dry ice and let the isopentane evaporate (note that this process takes on average around 15 - 20 min). Wrap the tissues in aluminum foil and store them at ultra low temperature (-70 °C to -80 °C) until sectioning.

2. Embedding the Tissues in OCT to Prepare Tissue Block

1. Transport tissues on dry ice to cyrostat to prevent thawing. Transfer tissue to cryostat chamber (set at -20 to -24 °C to avoid full thawing of tissues) and let them equilibrate for 30 min.
2. Turn the Peltier bay cooling on. If the cryostat does not have this cooling, use aerosol cooling spray to quickly freeze the OCT. Do not let the muscle thaw at any point during the embedding as this can result in freeze damage.
3. Add a uniform thin layer of OCT on the specimen disc and let it cool. When most of the OCT is frozen on the bottom while still liquid on the top, insert the tissue at the correct orientation (perpendicular to OCT for transverse sections and parallel to OCT for longitudinal sections). Use aerosol cooling spray to quickly freeze OCT. Touch the unembeded part of the tissue with heat extractor and wait for 45 sec.
4. Add another thin layer of OCT around the muscle, spray with aerosol cooling spray and extract the heat as in the previous step.
5. Keep adding OCT in small increments and quickly freeze the OCT using a combination of aerosol cooling spray and heat extractor until the whole muscle is covered.
6. Put the heat extractor on the top of the tissue block and wait for 5 min.

3. Preparing Sections and Identifying the Sections from Mid-belly Region of the Muscles

1. Mount the specimen onto the specimen head. Tighten the knob to secure the disc. Make sure that the specimen disc is in good contact with the specimen head.
2. Adjust the chamber temperature to between -21 and -24 °C and wait until the set temperature is achieved.
3. Adjust the thickness settings (7 µm); trim the block by advancing or retracting the block using coarse and fine settings.
4. Collect the sections on pre-warmed positively charged microscope slides by pressing the top of the slide onto the sections, using the attraction between opposite charges to facilitate the adherence of the cut sections to the slide.
5. Identify the mid-belly sections by measuring cross-sectional area (CSA) of the sections. Do this using imaging software on the computer that is connected to the microscope.
   NOTE: Phase contrast images are taken and circumference of the entire muscle is measured via a tracing function on the software program. This will yield both CSA as well as minimum ferret diameter (measure of fiber cross-sectional size that is expressed as the smallest distance between two parallel tangents on opposite sides of a particle) measurements. Note: When CSA and minimum ferret diameter measurements begin to plateau, mid belly has been reached.
6. Inventory and archive the slides at -80 °C for future staining.
   NOTE: OCT does not need to be removed prior to staining procedures. Once slides are coverslipped, they are ready to be stained immediately.

4. Staining

NOTE: While detailed step-by-step procedures can be found on the product data sheet and should be followed for staining procedures, personal optimization may be required to obtain optimal staining.

1. Because mounting media (see table) is not miscible with water, dehydrate slides through increasing grades of alcohol (2 min each in 70%, 95%, and 100% ethanol) and clear them with xylene (100% for 5 min) to ensure slides do not become opaque over time.
2. Coverslip sections and let them dry. Image with microscope equipped with imaging software.

Wyniki

The set-up for harvesting and freezing of tissues can be seen in Figure 1. Excised tissues should be stored on a gauze soaked in PBS to avoid drying (Figure 1A). When tissues are selected to be used for histological analysis they should be dipped in OCT and laid out on cryo mold in the proper orientation and as close to physiological length as possible to ensure accurate morphology (Figure 1B). Slurry of isopentane suitable for tissue freezing can be achieved by cooling ...

Dyskusje

Histology and immunohistochemistry have been used as key tools in understanding the manifestation and progression of pathology in various neuromuscular disorders. Classically, muscle biopsies were first fixed in formaldehyde and then embedded with paraffin wax. While formaldehyde fixation preserves tissue architecture and allows tissue storage and transport at RT, it also inactivates enzymes and crosslinks proteins necessitating further steps to achieve accurate immunostaining. This problem is eliminated with the use of ...

Materiały

Name	Company	Catalog Number	Comments
Cryostat	Leica CM 1850	Leica Microsystems Inc.	Buffalo Grove, IL 60089 U.S.A., office phone 1-800-248-0123 Alternative: Richard Allen Scientific
Microscope	Nikon Eclipse 50i	Nikon Instruments Inc.	1300 Walt Whitman Road, Melville, N.Y. 11747-3064 U.S.A., Phone: 1-631-547-8500 Alternative: Olympus
Image analysis software	Nikon Imaging Software Basic Research	Nikon Instruments Inc.	1300 Walt Whitman Road, Melville, N.Y. 11747-3064, U.S.A., Phone: 1-631-547-8500 Alternatives: Image J, Metamorph
Isoflurane	14043-220-05	JD Medical Dist. Co., Inc.	1923 West Peoria Avenue, Phoenix, AZ 85029 U.S.A.
OCT	4583	Sakura Inc.	Torrence, CA 90501 U.S.A. Alternative source: Leica Microsystem
Freeze It	23-022524	Thermofisher	790 Memorial Dr, Cambridge, MA, 02139 U.S.A. Alternative source: VWR Scientific
Disposable tissue mold	22-363-554	Thermofisher	790 Memorial Dr, Cambridge, MA 02139 U.S.A. Alternative source: VWR Scientific
Colorfrost plus slides	9991001	Thermofisher	790 Memorial Dr, Cambridge, MA 02139 U.S.A. Alternative source: VWR Scientific
Acetone	650501-4L	Sigma-Aldrich	3050 Spruce Street, St. Louis, MO 63103 U.S.A. Alternative source: VWR Scientific
Ethyl alcohol	HC-1300-1GL	Thermofisher	790 Memorial Dr, Cambridge, MA 02139 U.S.A. Alternative source: VWR Scientific
2-methyl butane	M 32631-SL	Sigma-Aldrich	3050 Spruce Street, St. Louis, MO 63103 U.S.A. Alternative source: VWR Scientific
Xylene	HC-7001GA	Thermofisher	790 Memorial Dr, Cambridge, MA 02139 U.S.A. Alternative source: VWR Scientific
Cytoseal 280	8311-4	Thermofisher	790 Memorial Dr, Cambridge, MA 02139 U.S.A. Alternative source: VWR Scientific
Hematoxylin Gill #3	CS402-1D	Thermofisher	790 Memorial Dr, Cambridge, MA 02139 U.S.A. Alternative source: VWR Scientific
Eosin	6766007	Thermofisher	790 Memorial Dr, Cambridge, MA 02139 U.S.A. Alternative source: VWR Scientific