4.3 Article

A Simplified Method for the Histochemical Detection of Iron in Paraffin Sections: Intracellular Iron Deposits in Central Nervous System Tissue

Journal

ASN NEURO
Volume 13, Issue -, Pages -

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/1759091420982169

Keywords

Alzheimer's disease; amyloid; CISD2; histochemistry; iron; mitochondria; neuron; paraffin; vessel

Categories

Funding

  1. ApoPharma, Inc.
  2. National Multiple Sclerosis Society [PP-1706-27915]
  3. University of Kansas Alzheimer's Disease Center (KU ADC) (National Institutes of Health) - National Institute on Aging [P30 AG035982]
  4. Kansas Intellectual and Developmental Disabilities Research Center [NIH U54 HD 090216]

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A simplified staining procedure incorporating acetone and limits to iron extraction was developed and applied to paraffin sections from CNS tissue of mice deficient in CISD2 and Alzheimer's disease cases. Discrete nuclear and cytoplasmic staining features were detected in neurons, particularly in hindbrain large neurons. The procedure revealed staining details often missed by other methods and could facilitate the study of iron in various CNS conditions.
Although all cells contain iron, most histochemical methods fail to reveal the presence of iron within many cells of the central nervous system (CNS), particularly neurons. Previously, a sensitive method was developed that limited the extraction of iron in paraffin sections, and this method revealed staining within neurons. However, the staining was often too robust making it difficult to discern discrete intracellular structures. In 1970, a study incorporated acetone in an iron histochemical procedure to facilitate the demarcation of staining features. In the present study, both acetone and limits to iron extraction were included in a simplified staining procedure. This procedure was applied to paraffin sections of CNS tissue from CISD2 deficient and littermate control mice. Discrete nuclear and cytoplasmic staining features were detected in all mice. Although widely present in neurons, punctate cytoplasmic staining was particularly prominent in large neurons within the hindbrain. Evaluation of extended depth of focus images, from serial focal planes, revealed numerous stained cytoplasmic structures. Additionally, the simplified staining procedure was applied to paraffin sections from Alzheimer's disease and control cases. Despite suboptimal processing conditions compared to mouse tissue, discrete staining of cytoplasmic structures was revealed in some neurons, although many other neurons had nondescript staining features. In addition, initial findings revealed iron deposited within some vessels from patients with Alzheimer's disease. In summary, since paraffin sections are commonly used for histological preparations, this simplified histochemical procedure could facilitate the study of iron in various CNS conditions by revealing staining details often missed by other procedures.

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