McKay Sarah M, Brooks Daniel J, Hu Ping, McLachlan Elspeth M
Spinal Injuries Research Centre, Prince of Wales Medical Research Institute, Randwick, NSW, Australia.
J Neuropathol Exp Neurol. 2007 Aug;66(8):698-710. doi: 10.1097/nen.0b013e3181256b32.
The inflammatory response has been characterized in the lumbosacral segments (L4-S1) of rats after spinal transection at T8. Immune cells were identified immunohistochemically using antibodies to complement type 3 receptor, CD11b (OX-42), the macrophage lysosomal antigen, CD68 (ED1), major histocompatibility complex class II (MHC II), and CD163 (ED2), a marker of perivascular cells. One week after cord transection, OX-42+ microglial density had nearly doubled. In the white matter, microglia became enlarged, often with retracted processes. In contrast, microglia in the grey matter remained ramified although nearly half of those lying medially contained clusters of ED1+ granules. After 8 weeks, ED1+ (+/-MHC II) macrophages were prominent in regions of Wallerian degeneration extending from dorsolateral to ventral funiculi. Microglial density remained raised in grey matter, particularly in the ventral horns of L4/5. Ramified microglia expressing MHC II+ (+/-ED1) extended from deep in the dorsal columns and around the central canal to the ventral columns. More ED2+ (+/-MHC II) perivascular and meningeal cells were recruited and expressed ED1. Thus, distinct from their conversion into macrophages in the white matter, the activation of ramified microglia after degeneration in the grey matter involves expression of ED1 without morphologic transformation.
在T8脊髓横断后的大鼠腰骶段(L4-S1)中对炎症反应进行了表征。使用针对补体3型受体CD11b(OX-42)、巨噬细胞溶酶体抗原CD68(ED1)、主要组织相容性复合体II类(MHC II)以及血管周围细胞标志物CD163(ED2)的抗体,通过免疫组织化学鉴定免疫细胞。脊髓横断一周后,OX-42 +小胶质细胞密度几乎增加了一倍。在白质中,小胶质细胞变大,其突起常常回缩。相比之下,灰质中的小胶质细胞仍呈分支状,尽管近一半位于内侧的小胶质细胞含有ED1 +颗粒簇。8周后,ED1 +(+/- MHC II)巨噬细胞在从背外侧到腹侧索的华勒氏变性区域中很突出。灰质中的小胶质细胞密度仍然升高,尤其是在L4/5的腹角。表达MHC II +(+/- ED1)的分支状小胶质细胞从背柱深处延伸至中央管周围并到达腹侧柱。更多的ED2 +(+/- MHC II)血管周围细胞和脑膜细胞被募集并表达ED1。因此,与它们在白质中转化为巨噬细胞不同,灰质变性后分支状小胶质细胞的激活涉及ED1的表达而无形态学转变。