High-Speed Human Temporal Bone Sectioning for the Assessment of COVID-19-Associated Middle Ear Pathology

Podsumowanie

This article describes a technique for rapid human temporal bone sectioning that utilizes a microsaw with twin diamond blades to generate thin slices for rapid decalcification and analysis of temporal bone immunohistochemistry.

Streszczenie

Histopathologic analysis of human temporal bone sections is a fundamental technique for studying inner and middle ear pathology. Temporal bone sections are prepared by postmortem temporal bone harvest, fixation, decalcification, embedding, and staining. Due to the density of the temporal bone, decalcification is a time-consuming and resource-intensive process; complete tissue preparation may take 9-10 months on average. This slows otopathology research and hinders time-sensitive studies, such as those relevant to the COVID-19 pandemic. This paper describes a technique for the rapid preparation and decalcification of temporal bone sections to speed tissue processing.

Temporal bones were harvested postmortem using standard techniques and fixed in 10% formalin. A precision microsaw with twin diamond blades was used to cut each section into three thick sections. Thick temporal bone sections were then decalcified in decalcifying solution for 7-10 days before being embedded in paraffin, sectioned into thin (10 µm) sections using a cryotome, and mounted on uncharged slides. Tissue samples were then deparaffinized and rehydrated for antibody staining (ACE2, TMPRSS2, Furin) and imaged. This technique reduced the time from harvest to tissue analysis from 9-10 months to 10-14 days. High-speed temporal bone sectioning may increase the speed of otopathology research and reduce the resources necessary for tissue preparation, while also facilitating time-sensitive studies such as those related to COVID-19.

Wprowadzenie

Human temporal bone research provides an invaluable resource to study the pathology and pathophysiology of the inner and middle ear. Before the 19th century, little was known regarding otologic disease^1,2,3. To better understand otologic disease and "rescue aural surgery from the hands of quacks," Joseph Toynbee (1815-1866) developed methods to study histologic sections of the human temporal bone³. This work was furthered by Adam Politzer (1835-1920) in Vienna and others across Europe during the remainder of the 19th century, who used temporal bone sections to describe the histopathology of many common conditions affecting the ear^2,3,4.

The first human temporal bone laboratory in the United States was opened in 1927 at Johns Hopkins Hospital, where Stacy Guild (1890-1966) developed methods for temporal bone sectioning^5,6. The methods developed by Guild consisted of a 9-10 month process that included postmortem harvest, fixation, decalcification in nitric acid, dehydration in ethanol, celloidin embedding, sectioning, staining, and mounting. Modifications to this technique were later made by Harold Schuknecht (1917-1996)⁷; however, the basic components of this process remain essentially unchanged.

The significant resources required to maintain a temporal bone laboratory have presented a challenge for temporal bone research and likely contributed to its declining popularity over the past 30 years^4,8. A significant portion of temporal bone laboratory resources must be devoted to the 9-10 month process of temporal bone preparation. One of the most time-consuming steps in preparation is the decalcification of the temporal bone, which is the densest bone in the human body. Decalcification is typically performed in nitric acid or ethylenediaminetetraacetic acid (EDTA) and takes weeks to months while requiring the frequent changing of solutions^7,9. Further, time-sensitive studies of the human ear, such as those related to the COVID-19 pandemic, may be hindered by this slow preparation process. This paper describes a technique for high-speed temporal bone sectioning that uses a diamond microsaw to generate thick sections that allow for rapid decalcification and tissue analysis within 10-14 days of temporal bone harvest.

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Protokół

This protocol was developed with IRB (IRB00250002) approval and in accordance with institutional policies for the use of human tissue and infectious material. Each temporal bone donor provided written consent before death, or consent was obtained posthumously from the donor's family. See the Table of Materials for details about all materials, equipment, and software used in this protocol.

1. Temporal bone harvest

1. Obtain local institutional review board (IRB) board approval, review institutional policies for the use of human and infectious material, and obtain consent for tissue donation before utilizing this protocol.
2. Put on proper personal protective equipment (PPE) before working with tissue from COVID-19-positive temporal bone donors. Ensure that the PPE consists of an N-95 respirator and face shield (or alternatively a positive pressure air purification system), gown, and two pairs of gloves. Review techniques for properly donning and doffing PPE before beginning this protocol¹⁰.
3. Harvest temporal bone tissue within 12-24 h of donor death. If the body is not refrigerated, ensure that the harvest occurs within 8 h of death.
   1. Harvest temporal bones during autopsy using the four-incision, block method by osteotome⁷.
      1. Following craniotomy, remove the brain and divide the cranial nerves to the internal auditory canal sharply.
      2. Make the first bony incision with the osteotome parallel to and just medial to the squamous portion of the temporal bone.
      3. Perform the second bony incision parallel to the first at the medial border of the temporal bone.
      4. Then, make the third incision 3-4 cm anterior and parallel to the petrous ridge.
      5. Make the fourth incision roughly parallel to the third, 2 cm posterior to the petrous ridge.
         NOTE: Ensure that all incisions extend through the skull base.
      6. Then, remove the temporal bone using sharp dissection to free the soft tissue attachment along the inferior edge of the specimen. If embalming is to be performed following temporal bone harvest, tie off the stump of the carotid artery.

2. Tissue fixation, decalcification, and sectioning

1. Immediately place the tissue in 200-300 mL of 10% buffered formalin (formaldehyde) so that the tissue is fully submerged. Leave the tissue in formaldehyde for a minimum of 72 h at room temperature, changing the solutions daily. Store the tissue in an air-tight container and perform solution changes under a fume hood while wearing appropriate PPE to prevent virus spread.
   NOTE: Following the 72 h fixation period, the specimens no longer need to be considered infectious.
2. Use a precision microsaw with twin diamond blades to cut each specimen into three "thick" sections to allow for more rapid tissue decalcification. Set the twin diamond blades to a distance of 5 mm, so that the central section of temporal bone is 5 mm thick. Ensure that the sections of tissue on either end are 3-5 mm thick.
3. Place the thick sections in 200-300 mL of 23% w/w formic acid decalcifying solution for 7-10 days at room temperature, until the tissue is soft enough for paraffin embedding. Change the solutions daily. Check for adequate tissue decalcification by palpating the specimen, which should feel soft.
   NOTE: Decalcification may also be verified by x-ray.
4. Rinse the specimens in running tap water for 24 h by placing them in a large beaker underneath a running faucet.
5. Dehydrate the tissue in a series of alcohols of increasing concentration⁷. Submerge the tissue in 100-200 mL of 70% ethanol for 1.5 h, followed by three washes in 95% and 100% ethanol for 1.5 h each, respectively. Next, wash the tissue 3 x 1.5 h in Xylene.
6. Embed the thick sections in paraffin, with four treatments of 45 min each.
7. Use a cryotome to cut thin (10 µm) sections. Position the tissue so that the tissue is cut in the axial plane. Cut thicker (20 µm) sections if desired.

3. Immunohistochemistry and imaging

1. If traditional hematoxylin and eosin staining is desired (not described here), perform staining before mounting the sections on glass slides⁷.
2. Mount the sections on positively charged glass slides.
3. Bake the slides on a hot plate at 60 °C for 20 min.
4. Place the slides in a holder and submerge them in a commercial pretreatment solution containing an organic solvent (diethanolamine in this case) and ethanol to deparaffinize, rehydrate, and unmask the tissue.
   NOTE: This step is necessary to achieve satisfactory results with immunohistochemistry for formalin-fixed and paraffin-embedded tissue.
5. Heat the slides in a pressure cooker on high pressure for 20 min.
6. Place the slides in a humidified chamber and block the tissue with a commercial blocking solution.
7. Probe the tissue sections with the primary antibody against angiotensin-converting enzyme 2 (ACE2; 1:50), transmembrane protease serine 2 (TMPRSS2, 1:1,000), and the Furin protease (1:250).
   NOTE: The ACE2, TMPRSS2, and Furin antibodies are used because these proteins are believed to play a role in SARS-CoV-2 infectivity^11,12, and this protocol sought to investigate the possible mechanisms by which SARS-CoV-2 may infect the middle ear¹³.
8. Treat with HRP-conjugated anti-rabbit secondary antibody (ACE2, Furin; 1:100 dilution) or anti-goat (TMPRSS2, 1:100 dilution) secondary antibody.
9. Counterstain the slides with 70% hematoxylin in water.
10. Acquire images on a light microscope with a mounted digital camera. Obtain images of the middle ear mucosa and Eustachian tube at 20x and 10x magnification, respectively.

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Wyniki

Hematoxylin and eosin staining of the middle ear mucosa and Eustachian tube showed preservation of the middle ear mucosa and submucosal middle ear tissue following processing (Figure 1). Immunohistochemical images showed expression of the ACE2, TMPRSS2, and Furin proteins within the middle ear mucosa and Eustachian tube (Figure 1). The presence of these proteins within the middle ear provides a possible route by which SARS-CoV-2 may infect the respiratory epithe...

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Dyskusje

Human temporal bone research is critical for studying inner and middle ear pathology but remains a time- and resource-intensive endeavor. This paper describes a technique that uses a diamond microsaw to generate thick temporal bone sections that can be rapidly decalcified before further sectioning so that the time from tissue harvest to study can be reduced from 9-10 months to 10-14 days. This technique may reduce the resources required for temporal bone processing and facilitate time-sensitive studies, such as those rel...

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Materiały

Name	Company	Catalog Number	Comments
Anti-ACE-2 Antibody (1:50 applied dilution)	Novus Biologicals	SN0754
Anti-Furin Antibody (1:250 dilution)	Abcam	EPR 14674
Anti-TMPRSS2 Antibody (1:1,000 dilution)	Novus Biologicals	NBP1-20984
BX43 Manual System Microscope	Olympus Life Science Solutions
CBN/Diamond Hybrid Wafering Blade	Pace Technologies	WB-007GP
Collin Mallet - 8''	Surgical Mart	SM1517
DS-Fi3 Microscope Camera	Nikon
Dual Endogenous Enzyme Block (commercial blocking solution)	Dako	S2003
Eaosin Stain	Sigma-Aldrich	548-24-3
Formalin solution, neutral buffered 10%	Sigma-Aldrich	HT501128
Formical-4 Decalcifier (formic acid decalcifying solution)	StatLab	1214-1 GAL
Hematoxylin Stain	Sigma-Aldrich	H9627
HRP-Conjugated Anti-Rabbit Secondary Antibody (1:100 dilution)	Leica Biosystems	PV6119
ImmPRESS HRP Horse Anti-Goat igG Detection Kit, Peroxidase (1:100 dilution)	Vector Laboratories	MP-7405
Lambotte Osteotome	Surgical Mart	SM1553
Metallographic PICO 155P Precision Saw	Pace Technologies	PICO 155P	microsaw
NIS Elements Software Version 4.6	Nikon
Paraplast Plus	Sigma-Aldrich	P3683	paraffin
Positive Charged Microscope Slides with White Frosted End	Walter Products	1140B15
Thermo Shandon Crytome FSE Cryostat Microtome	New Life Scientific Inc.	A78900104	cryotome
Triology Pretreatment Solution (commercial pretreatment solution)	Sigma-Aldrich	920P-05
Xylene	Sigma-Aldrich	920P-05