Pial Vessel-Associated Microglia/Macrophages Increase in Female Dahl-SS/Jr Rats Independent of Pregnancy History.
Pial Vessel-Associated Microglia/Macrophages Increase in Female Dahl-SS/Jr Rats Independent of Pregnancy History.
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与妊娠史无关的女性DAHL-SS/JR大鼠的小血管相关小胶质细胞/巨噬细胞增加。
DOI:
10.3390/ijms23063384
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发表时间:
2022-03-21
影响因子:
5.6
通讯作者:
Sasser JM
中科院分区:
文献类型:
--
作者:
Warrington JP;Shao Q;Clayton AM;Maeda KJ;Beckett AG;Garrett MR;Sasser JM
As the resident immune cells of the central nervous system, microglia have a wide range of functions such as surveillance, phagocytosis, and signaling through production of chemokines and cytokines. Recent studies have identified and characterized macrophages residing at the meninges, a series of layers surrounding the brain and spinal cord. While perivascular microglia within the brain parenchyma increase following chronic hypertension, there are no reports of changes at the meninges, and specifically, associated with the pial vasculature. Thus, we used female Sprague Dawley and Dahl salt-sensitive (SS/Jr) rat brains, stained for ionized calcium-binding adapter molecule (Iba1), and characterized microglia/macrophages associated with pial vessels in the posterior brain. Results indicate that Iba1+ pial vessel-associated microglia (PVAM) completely surrounded the vessels in brains from the Dahl-SS/Jr rats. PVAM density was significantly higher and distance between PVAMs lower in Dahl-SS/Jr compared to the Sprague Dawley rat brains. Pregnancy history did not affect these findings. While the functional role of these cells are not known, we contextualize our novel findings with that of other studies assessing or characterizing myeloid cells at the borders of the CNS (meninges and choroid plexus) and perivascular macrophages and propose their possible origin in the Dahl-SS/Jr model of chronic hypertension.
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影响因子:
8.8
作者:
Askew K;Li K;Olmos-Alonso A;Garcia-Moreno F;Liang Y;Richardson P;Tipton T;Chapman MA;Riecken K;Beccari S;Sierra A;Molnár Z;Cragg MS;Garaschuk O;Perry VH;Gomez-Nicola D
通讯作者:
Gomez-Nicola D
影响因子:
56.9
作者:
Nimmerjahn, A;Kirchhoff, F;Helmchen, F
通讯作者:
Helmchen, F
DOI:
10.1016/j.bbi.2018.03.028
发表时间:
2018-05
期刊:
Brain, behavior, and immunity
影响因子:
--
作者:
Clayton AM;Shao Q;Paauw ND;Giambrone AB;Granger JP;Warrington JP
通讯作者:
Warrington JP
影响因子:
8.3
作者:
Hung SK;Lee MS;Lin HY;Chen LC;Chuang CJ;Chew CH;Yu BH;Yang HJ;Hsu FC;Chiou WY
通讯作者:
Chiou WY
DOI:
10.1016/s0169-328x(98)00040-0
发表时间:
1998-06-01
期刊:
MOLECULAR BRAIN RESEARCH
影响因子:
--
作者:
Ito, D;Imai, Y;Kohsaka, S
通讯作者:
Kohsaka, S