Ultrasound-accelerated Tissue Fixation/Processing Achieves Superior Morphology and Macromolecule Integrity with Storage Stability

Author:

Chu Wei-Sing1,Liang Qi1,Tang Yao2,King Randy1,Wong Kondi3,Gong Maokai1,Wei Minqi1,Liu Jilan1,Feng Shaw-Huey4,Lo Shyh-Ching4,Andriko Jo-Ann5,Orr Marshall6

Affiliation:

1. Department of Scientific Laboratories, Armed Forces Institute of Pathology, Washington, DC

2. Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland

3. Neuropathology and Ophthalmic Pathology, Armed Forces Institute of Pathology, Washington, DC

4. Infectious and Parasitic Diseases Pathology, Armed Forces Institute of Pathology, Washington, DC

5. Department of Pathology, Walter Reed Army Medical Center, Washington, DC

6. Naval Research Laboratory, Washington, DC

Abstract

We demonstrate that high-frequency and high-intensity ultrasound (US) can be applied to both tissue fixation and tissue processing to complete the conventional overnight formalin-fixation and paraffin-embedding (FFPE) procedures within 1 hr. US-facilitated FFPE retains superior tissue morphology and long-term room temperature storage stability than conventional FFPE. There is less alteration of protein antigenicity after US-FFPE preservation so that rapid immunohistochemical reactions occur with higher sensitivity and intensity, reducing the need for antigen retrieval pretreatment. US-FFPE tissues present storage stability so that room temperature storage up to 7 years does not significantly affect tissue morphology, protein antigenic properties, RNA distribution, localization, and quantitation. In addition, during fixation, tissue displays physical changes that can be monitored and reflected as changes in transmission US signals. As far as we know, this is the first effort to monitor tissue physical changes during fixation. Further study of this phenomenon may provide a method to control and to monitor the level of fixation for quality controls. The mechanism of less alteration of protein antigenicity by US-FFPE was discussed. (J Histochem Cytochem 54:503-513, 2006)

Publisher

SAGE Publications

Subject

Histology,Anatomy

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