首页> 美国卫生研究院文献>Frontiers in Neurology >Vasculature Remodeling in a Rat Model of Cerebral Ischemia. The Fate of the BrdU-Labeled Cells Prior to Stroke
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Vasculature Remodeling in a Rat Model of Cerebral Ischemia. The Fate of the BrdU-Labeled Cells Prior to Stroke

机译:在大鼠脑缺血模型中的血管重构。脑卒中前BrdU标签细胞的命运

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摘要

Despite the clinical significance of post-stroke angiogenesis, a detailed phenotypic analysis of pre-stroke vascular remodeling and post-stroke angiogenesis had not yet been done in a model of focal ischemia. In this study, using BrdU-labeling of proliferating cells and immunofluorescence of pre- and post-stroke rats, we found that, (i) BrdU administered before stroke was incorporated preferentially into the nuclei of endothelial cells lining the lumen of existing blood vessels and newly born neurons in the dentate gyrus but not in the subventricular zone or proliferating microglia, (ii) BrdU injection prior to stroke led to the patchy distribution of the newly incorporated endothelial cells into existing blood vessels of the adult rat brain, (iii) BrdU injection prior to stroke specifically labeled neuronal precursors cells in a region of soft tissue beyond the inhibitory scar, which seems to be permissive to regenerative events, (iv) BrdU injection after stroke led to labeling of endothelial cells crossing or detaching from the disintegrating blood vessels and their incorporation into new blood vessels in the stroke region, scar tissue and the region beyond, (v) BrdU injection after stroke led to specific incorporation of BrdU-positive nuclei into the “pinwheel” architecture of the ventricular epithelium, (vi) blood vessels in remote areas relative to the infarct core and in the contralateral non-lesioned cortex, showed co-labeled BrdU/RECA+ endothelial cells shortly after the BrdU injection, which strongly suggests a bone marrow origin of the endothelial cells. In the damaged cortex, a BrdU/prolyl 4-hydroxylase beta double labeling in the close proximity to collagen IV-labeled basement membrane, suggests that, in addition to bone marrow derived endothelial cells, the disintegrating vascular wall itself could also be a source of proliferating endothelial cells, (vii) By day 28 after stroke, new blood vessels were observed in the perilesional area and the scar tissue region, which is generally considered to be resistant to regenerative events. Finally, (viii) vigorous angiogenesis was also detected in a region of soft tissue, also called “islet of regeneration,” located next to the inhibitory scar.>Conclusion: BrdU administered prior to, and after stroke, allows to investigate brain vasculature remodeling in the adult brain.
机译:尽管中风后血管生成具有临床意义,但尚未在局灶性缺血模型中对中风前血管重塑和中风后血管生成进行详细的表型分析。在这项研究中,我们使用BrdU标记增生性细胞以及中风前和中风后大鼠的免疫荧光,我们发现:(i)中风前施用的BrdU被优先掺入衬在现有血管腔内的内皮细胞核中。齿状回中的新生神经元,但不在脑室下区域或增殖性小胶质细胞中,(ii)脑卒中前的BrdU注射导致新整合的内皮细胞向成年大鼠脑的现有血管中分散分布,(iii)BrdU在卒中前注射特别标记的神经元前体细胞在抑制性瘢痕之外的软组织区域中,这似乎允许再生事件。(iv)在卒中后进行BrdU注射导致内皮细胞的标记穿越或脱离崩解血管(v)中风后注射BrdU,并将其整合到中风区域,疤痕组织及其他区域的新血管中导致BrdU阳性细胞核特异性掺入心室上皮的“风车”结构。(vi)相对于梗塞核心和对侧非病变皮层的偏远地区的血管,显示出共同标记的BrdU / RECA BrdU注射后不久 + 内皮细胞,强烈暗示了内皮细胞的骨髓起源。在受损的皮层中,紧邻胶原IV标记的基底膜的BrdU /脯氨酰4-羟化酶β双标记表明,除骨髓来源的内皮细胞外,崩解的血管壁本身也可能是血管壁的来源。 (vii)卒中后第28天,在病灶周围区域和瘢痕组织区域观察到了新血管,通常认为该血管对再生事件具有抵抗力。最后,(viii)在抑制性瘢痕旁的软组织区域(也称为“再生岛”)也检测到了强烈的血管生成。>结论:在卒中前后,给予BrdU,可以研究成人大脑中的脑血管重构。

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