TMEM119 as a specific marker of microglia reaction in traumatic brain injury in postmortem examination

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TMEM119 as a specific marker of microglia reaction in traumatic brain injury in postmortem examination. / Bohnert, Simone; Seiffert, Anja; Trella, Stefanie; Bohnert, Michael; Distel, Luitpold; Ondruschka, Benjamin; Monoranu, Camelia-Maria.

In: INT J LEGAL MED, Vol. 134, No. 6, 11.2020, p. 2167-2176.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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Bohnert, S, Seiffert, A, Trella, S, Bohnert, M, Distel, L, Ondruschka, B & Monoranu, C-M 2020, 'TMEM119 as a specific marker of microglia reaction in traumatic brain injury in postmortem examination', INT J LEGAL MED, vol. 134, no. 6, pp. 2167-2176. https://doi.org/10.1007/s00414-020-02384-z

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@article{1d3227b777ef4ad987f34ebf8794c685,
title = "TMEM119 as a specific marker of microglia reaction in traumatic brain injury in postmortem examination",
abstract = "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.",
author = "Simone Bohnert and Anja Seiffert and Stefanie Trella and Michael Bohnert and Luitpold Distel and Benjamin Ondruschka and Camelia-Maria Monoranu",
year = "2020",
month = nov,
doi = "10.1007/s00414-020-02384-z",
language = "English",
volume = "134",
pages = "2167--2176",
journal = "INT J LEGAL MED",
issn = "0937-9827",
publisher = "Springer",
number = "6",

}

RIS

TY - JOUR

T1 - TMEM119 as a specific marker of microglia reaction in traumatic brain injury in postmortem examination

AU - Bohnert, Simone

AU - Seiffert, Anja

AU - Trella, Stefanie

AU - Bohnert, Michael

AU - Distel, Luitpold

AU - Ondruschka, Benjamin

AU - Monoranu, Camelia-Maria

PY - 2020/11

Y1 - 2020/11

N2 - 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.

AB - 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.

U2 - 10.1007/s00414-020-02384-z

DO - 10.1007/s00414-020-02384-z

M3 - SCORING: Journal article

C2 - 32719959

VL - 134

SP - 2167

EP - 2176

JO - INT J LEGAL MED

JF - INT J LEGAL MED

SN - 0937-9827

IS - 6

ER -