Differential Leukocyte and Platelet Profiles in Distinct Models of Traumatic Brain Injury.
Differential Leukocyte and Platelet Profiles in Distinct Models of Traumatic Brain Injury.
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DOI:
10.3390/cells10030500
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发表时间:
2021-02-26
期刊:
影响因子:
6
通讯作者:
Sullivan PG
中科院分区:
文献类型:
--
作者:
Hubbard WB;Banerjee M;Vekaria H;Prakhya KS;Joshi S;Wang QJ;Saatman KE;Whiteheart SW;Sullivan PG
Traumatic brain injury (TBI) affects over 3 million individuals every year in the U.S. There is growing appreciation that TBI can produce systemic modifications, which are in part propagated through blood–brain barrier (BBB) dysfunction and blood–brain cell interactions. As such, platelets and leukocytes contribute to mechanisms of thromboinflammation after TBI. While these mechanisms have been investigated in experimental models of contusion brain injury, less is known regarding acute alterations following mild closed head injury. To investigate the role of platelet dynamics and bioenergetics after TBI, we employed two distinct, well-established models of TBI in mice: the controlled cortical impact (CCI) model of contusion brain injury and the closed head injury (CHI) model of mild diffuse brain injury. Hematology parameters, platelet-neutrophil aggregation, and platelet respirometry were assessed acutely after injury. CCI resulted in an early drop in blood leukocyte counts, while CHI increased blood leukocyte counts early after injury. Platelet-neutrophil aggregation was altered acutely after CCI compared to sham. Furthermore, platelet bioenergetic coupling efficiency was transiently reduced at 6 h and increased at 24 h post-CCI. After CHI, oxidative phosphorylation in intact platelets was reduced at 6 h and increased at 24 h compared to sham. Taken together, these data demonstrate that brain trauma initiates alterations in platelet-leukocyte dynamics and platelet metabolism, which may be time- and injury-dependent, providing evidence that platelets carry a peripheral signature of brain injury. The unique trend of platelet bioenergetics after two distinct types of TBI suggests the potential for utilization in prognosis.
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影响因子:
4.6
作者:
Hubbard, W. Brad;Harwood, Christopher L.;Sullivan, Patrick G.
通讯作者:
Sullivan, Patrick G.
DOI:
10.1097/nen.0000000000000115
发表时间:
2014-10
影响因子:
3.2
作者:
Bolton AN;Saatman KE
通讯作者:
Saatman KE
影响因子:
1.9
作者:
Guillotte, Andrew R.;Herbert, Joseph P.;Litofsky, N. Scott
通讯作者:
Litofsky, N. Scott
影响因子:
6.9
作者:
Chodobski A;Zink BJ;Szmydynger-Chodobska J
通讯作者:
Szmydynger-Chodobska J
影响因子:
16.6
作者:
Ehinger JK;Piel S;Ford R;Karlsson M;Sjövall F;Frostner EÅ;Morota S;Taylor RW;Turnbull DM;Cornell C;Moss SJ;Metzsch C;Hansson MJ;Fliri H;Elmér E
通讯作者:
Elmér E