Abstract

Laser microdissection is an invaluable tool in medical research that facilitates collecting specific cell populations for molecular analysis. Diversity of research targets (e.g., cancerous and precancerous lesions in clinical and animal research, cell pellets, rodent embryos, etc.) and varied scientific objectives, however, present challenges toward establishing standard laser microdissection protocols. Sample preparation is crucial for quality RNA, DNA and protein retrieval, where it often determines the feasibility of a laser microdissection project. The majority of microdissection studies in clinical and animal model research are conducted on frozen tissues containing native nucleic acids, unmodified by fixation. However, the variable morphological quality of frozen sections from tissues containing fat, collagen or delicate cell structures can limit or prevent successful harvest of the desired cell population via laser dissection. The CryoJane Tape-Transfer System®, a commercial device that improves cryosectioning outcomes on glass slides has been reported superior for slide preparation and isolation of high quality osteocyte RNA (frozen bone) during laser dissection. Considering the reported advantages of CryoJane for laser dissection on glass slides, we asked whether the system could also work with the plastic membrane slides used by UV laser based microdissection instruments, as these are better suited for collection of larger target areas. In an attempt to optimize laser microdissection slide preparation for tissues of different RNA stability and cryosectioning difficulty, we evaluated the CryoJane system for use with both glass (laser capture microdissection) and membrane (laser cutting microdissection) slides. We have established a sample preparation protocol for glass and membrane slides including manual coating of membrane slides with CryoJane solutions, cryosectioning, slide staining and dissection procedure, lysis and RNA extraction that facilitated efficient dissection and high quality RNA retrieval from CryoJane preparations. CryoJane technology therefore has the potential to facilitate standardization of laser microdissection slide preparation from frozen tissues.

Highlights

  • Laser microdissection (LM) of frozen tissue sections has been successfully used for genomic and proteomic studies in clinical and research laboratories [1,2,3]

  • Considering that the CryoJane procedure aids in successful serial sectioning of a frozen tissue block and in protecting tissue RNA due to the low temperature (225–30uC) of cryotomy, we evaluated CryoJane for the optimization of LM sample preparation for frozen tissues

  • PET-CJ slide should be placed on a MMI SupportSlide, which proved to be invaluable for proper transfer of sections onto membranes during application of the Hand Roller (Leica Microsystems, GmbH, Nussloch, Germany) to the Transfer Adhesive Tape

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Summary

Introduction

Laser microdissection (LM) of frozen tissue sections has been successfully used for genomic and proteomic studies in clinical and research laboratories [1,2,3]. Frozen sections are considered optimal for genomic studies [2,5,7,8], but a range of tissues containing collagen, fat, cartilage, bone and delicate structures (e.g. mouse normal ovarian epithelium) as well as plant tissues are not suitable for routine serial cryosectioning. For such tissues, random loss of material during cryotomy and staining, as well as poor section morphology is common [9]

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