U54 SCENT Normal Lung Autopsy Tissue Collection Procedure
Carolyn Glass, andrew.nixon, Mary Jordan*
Abstract
This document outlines the required criteria and collection protocol for normal lung specimen acquisition from autopsy at Duke University Hospital through the Biorepository and Precision Pathology Center (BRPC) in the Department of Pathology.
Steps
Inclusion and Exclusion Criteria
Inclusion Criteria:
• >18 weeks fetal lung to age >85 years old from decedents with consented autopsy
• All sexes
• Grossly normal lung (reviewed and triaged by autopsy staff/faculty)
Exclusion Criteria:
• No primary lung disease (pulmonary embolism, COPD, primary lung cancer,
pneumonia, interstitial lung disease, emphysema/heavy smoker, etc)
• If “pulmonary hypertension” stated in clinical notes, this tissue maystill be taken and
reviewed by histologic exam
• No metastatic cancer to lung
• No active infection (remote >2 weeks ago is acceptable, viral titers must be negative)
• Check blood culture for infection
• No recent treatment with chemotherapy (recent <1 year)
• Time of death <48 hours prior to collection
Collection Protocol
U54 Clinical Research Coordinator will access Microsoft Teams DUH Decedent Care - Labs Autopsy Team.
U54 Clinical Research Coordinator will screen the afternoon prior for upcoming autopsy collections that fit inclusion and exclusion criteria.
U54 Clinical Research Coordinator will call the morning of procedure day at to request for resident or PA for:
a. Lung tissue available from autopsy
b. Before and after pictures of lungs
Before and after pictures of lungs
b.
Autopsy team will notify BRPC staff of available tissue.
Receive 1 fragment of normal lung tissue (total size collected will be 3x3x3 cm) from the RUL, RML, RLL, LUL, and LLL upon notification by the autopsy suite staff.
Process each lobe fragment into the following samples. Create a QC for each sample collected
a. FFPE (3x3x0.5 cm)
b. Snap frozen: split in half
9. ½ snap freeze in cryovial
ii. ½ will be cut into “rice -size piece”
1. Wash tissue with PBS to remove the blood and epithelial lining fluid.
2. Using blade, mince tissue into approximately 20 small pieces (1-2mm).
3. Evenly distribute the rice sized pieces into 3 cryopreserved tubes with 1mL freezing media
each.
4. Cells should be frozen slowly at 1°C/min. Put tubes in the freezing container (e.g.,
Mr. Frosty) with isopropyl alcohol and place them overnight in a -80'C freezer.
5. Next day, transfer tubes to liquid nitrogen.
c. If tissue remaining: 3 additional cryovials of snap frozen tissue cut into rice sized pieces and
OCT
Route FFPE samples to Research Histology Lab to:
a. Create an H&E from each FFPE sample and route to pathologist for review.
b. After review, create 2 tissue scrolls from the tissue blocks and coordinate RNA and DNA
extraction.
c. Once RNA and DNA extraction is complete, the frozen LN2 samples will be shipped to lab for
scRNAseq.