Evidence map›Paper›PMID 39611118›Full record

ArticleFrontiers in neuroanatomy2024

Differential effects of prolonged post-fixation on immunohistochemical and histochemical staining for postmortem human brains.

Weiya Ma, Eve-Marie Frigon, Josefina Maranzano, Yashar Zeighami, Mahsa Dadar

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Article in Frontiers in neuroanatomy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Weiya MaCerebral Imaging Centre, Douglas Mental Health University Institute, Montreal, QC, Canada.
Eve-Marie FrigonDepartment of Anatomy, University of Quebec in Trois-Rivieres, Trois-Rivieres, QC, Canada.
Josefina MaranzanoDepartment of Anatomy, University of Quebec in Trois-Rivieres, Trois-Rivieres, QC, Canada.
Yashar ZeighamiCerebral Imaging Centre, Douglas Mental Health University Institute, Montreal, QC, Canada.
Mahsa DadarCerebral Imaging Centre, Douglas Mental Health University Institute, Montreal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Immunohistochemical (IHC) and histochemical (HC) staining techniques are widely used on human brains that are post-fixed in formalin and stored in brain banks worldwide for varying durations, from months to decades. Understanding the effects of prolonged post-fixation, postmortem interval (PMI), and age on these staining procedures is important for accurately interpreting their outcomes, thereby improving the diagnosis and research of brain disorders afflicting millions of people worldwide. Methods: In this study, we conducted both IHC and HC staining on the prefrontal cortex of postmortem human brains post-fixed for 1, 5, 10, 15, and 20 years. For IHC staining, we used two antibodies for each marker: the neuron marker neuronal nuclear antigen (NeuN), the astrocyte marker glial fibrillary acidic protein (GFAP), and the microglia marker ionized calcium-binding adaptor molecule 1 (Iba1). For HC staining, we conducted hematoxylin and eosin Y (H&E), cresyl violet (CV), and Luxol fast blue (LFB) stains to examine neuropils, neurons, and myelin, respectively. Results: We observed that the intensity of NeuN, Iba1, CV, or LFB staining was negatively correlated with post-fixation durations. Conversely, we detected a positive correlation between the intensity of GFAP and H&E staining and post-fixation durations. Moreover, there was no correlation between the intensity of NeuN, GFAP, Iba1, H&E, CV, and LFB staining and PMI. Additionally, no correlation was found between these staining intensities and age, except for the intensity of GFAP immunostained by one antiserum, which was negatively correlated with age. Conclusion: Taken together, these findings suggest that prolonged post-fixation has both positive and negative effects, while age and PMI exert limited influence on these IHC and HC parameters. Therefore, it is essential to consider these differential changes when interpreting results derived from tissues with extended post-fixation durations. Furthermore, if feasible, we recommend conducting IHC and HC staining on human brains with the same post-fixation time spans and using the most optimal antibodies to mitigate the impact on subsequent analyses.

Indexed as

brain bankGFAPhematoxylinIba1myelinNeuNpostmortem intervalprefrontal cortex

Identifiers

PMID39611118
PMCPMC11602276

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