TMEM119 as a specific marker of microglia reaction in traumatic brain injury in postmortem examination
Autor: | Stefanie Trella, Camelia-Maria Monoranu, Luitpold Distel, Simone Bohnert, Michael Bohnert, Benjamin Ondruschka, Anja Seiffert |
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Rok vydání: | 2020 |
Předmět: |
Male
Pathology 0302 clinical medicine Cerebrospinal fluid Cerebellum Pons Cortex (anatomy) Brain Injuries Traumatic Receptors Immunologic Child Forensic Pathology Aged 80 and over 0303 health sciences Membrane Glycoproteins Microglia Human brain Middle Aged Immunohistochemistry White Matter medicine.anatomical_structure Child Preschool Female Original Article Autopsy Immunocytochemistry Adult medicine.medical_specialty Adolescent Receptors CCR2 Traumatic brain injury Pathology and Forensic Medicine White matter Young Adult 03 medical and health sciences medicine Humans ddc:610 Neuroinflammation Aged 030304 developmental biology Forensic neuropathology business.industry Membrane Proteins Biomarker medicine.disease Forensic neurotraumatology business Biomarkers 030217 neurology & neurosurgery |
Zdroj: | International Journal of Legal Medicine |
ISSN: | 1437-1596 0937-9827 |
DOI: | 10.1007/s00414-020-02384-z |
Popis: | The aim of the present study was a refined analysis of neuroinflammation including TMEM119 as a useful microglia-specific marker in forensic assessments of traumatic causes of death, e.g., traumatic brain injury (TBI). Human brain tissue samples were obtained from autopsies and divided into cases with lethal TBI (n = 25) and subdivided into three groups according to their trauma survival time and compared with an age-, gender-, and postmortem interval-matched cohort of sudden cardiovascular fatalities as controls (n = 23). Brain tissue samples next to cortex contusions and surrounding white matter as well as samples of the ipsilateral uninjured brain stem and cerebellum were collected and stained immunohistochemically with antibodies against TMEM119, CD206, and CCR2. We could document the highest number of TMEM119-positive cells in acute TBI death with highly significant differences to the control numbers. CCR2-positive monocytes showed a significantly higher cell count in the cortex samples of TBI cases than in the controls with an increasing number of immunopositive cells over time. The number of CD206-positive M2 microglial cells increased survival time-dependent. After 3 days of survival, the cell number increased significantly in all four regions investigated compared with controls. In sum, we validate a specific and robustly expressed as well as fast reacting microglia marker, TMEM119, which distinguishes microglia from resident and infiltrating macrophages and thus offers a great potential for the estimation of the minimum survival time after TBI. Electronic supplementary material The online version of this article (10.1007/s00414-020-02384-z) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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