Constructing high-density tissue microarrays with a novel method and a self-made tissue-arraying instrument

Abstract

Abstract Tissue microarrays (TMAs), also called tissue chips, contain hundreds to thousands of tissue cores obtained from different tissue donor blocks. By using TMA technology, a molecular marker, such as protein, RAN or DNA, can be simultaneously examined in hundreds of different specimens under the same experimental conditions. A growing number of previous studies have introduced different methods for constructing TMAs. Many authors tried to use various methods to implant more tissue cores in a single recipient block, and most of these methods involved reducing the diameter of the tissue cores and/or the spacing between adjacent tissue cores. However, when creating TMAs, it is difficult to reduce the distance between tissue cores to zero except with extremely expensive automatic TMA arrayers. Here, we introduce a novel method to construct a high-density TMA that does not have spacing between the tissue cores. We also introduce a method for preparing a self-made tissue‑arraying instrument. With this method and the tissue‑arraying instrument, we successfully created a TMA containing 126 tissue cores that were 2 mm in diameter. H&E staining, immunohistochemical staining and fluorescence in situ hybridization were performed on the sections cut from the TMA without any tissue spot loss. This method is easy to operate, and the materials for creating the tissue‑arraying instrument are inexpensive and can be purchased anywhere. Therefore, this high-density method can be applied in all laboratories.