《中国康复理论与实践》 ›› 2019, Vol. 25 ›› Issue (11): 1293-1302.doi: 10.3969/j.issn.1006-9771.2019.11.008

• 基础研究 • 上一篇    下一篇

脑梗死后囊腔微环境分析

李秀明1, 刘罡2   

  1. 1.上海交通大学医学院附属瑞金医院北院,上海市 201801
    2.复旦大学附属华山医院,上海市 200031
  • 收稿日期:2019-04-22 修回日期:2019-07-12 出版日期:2019-11-25 发布日期:2019-11-21
  • 通讯作者: 刘罡,E-mail: surgeonliu@126.com E-mail:surgeonliu@126.com
  • 作者简介:李秀明(1984-),女,汉族,山东滨州市人,硕士,主治医师,主要研究方向:脑卒中的康复治疗、骨关节疾病康复等。
  • 基金资助:
    上海市卫计委课题(No. 20154Y0101)

Microenvironment Analysis of Cystic Cavity after Cerebral Infarction

LI Xiu-ming1, LIU Gang2   

  1. 1.North Hospital of Ruijin Hospital Affiliated to Medical College of Shanghai Jiaotong University, Shanghai 201801, China
    2.Huashan Hospital Affiliated to Fudan University, Shanghai 200031, China
  • Received:2019-04-22 Revised:2019-07-12 Published:2019-11-25 Online:2019-11-21
  • Contact: LIU Gang, E-mail: surgeonliu@126.com E-mail:surgeonliu@126.com
  • Supported by:
    Supported by Shanghai Health and Family Planning Committee Research Project (No. 20154Y0101)

摘要: 目的 研究脑梗死囊腔内液化学成分和囊腔壁血供情况,分析其是否适宜神经干细胞移植。方法 雄性Sprague-Dawley大鼠20只行永久性大脑中动脉栓塞术。造模后3 d、10 d、21 d MRI观察梗死后囊腔形成情况,获取囊腔和侧脑室坐标。形成囊腔的大鼠抽取囊腔内液和脑脊液质谱分析。鼠脑HE染色和免疫荧光凝集素染色进行观察。结果 造模后21 d时,大鼠脑梗死区液体囊腔形态基本稳定。囊腔由坏死区周边正常脑组织与软脑膜共同构成。囊腔中心无细胞结构存在;囊腔壁部分由软脑膜构成,脑膜结构完整,其上可见脑膜血管;囊腔中心与脑膜交界处可见大量细胞聚集。囊腔周围有血管分布,与对侧相应脑区无明显差别。与脑脊液相比,囊腔微环境中共筛选出36种差异分子,31种上升,5种下降。差异最大的10种分子中,多数对干细胞移植具有正面促进作用,包括抗炎、抗肿瘤、促进神经细胞存活等。但缺乏促进神经干细胞向神经元分化的相关分子,促进向胶质增生的相关分子增高。结论 脑梗死慢性期形成的囊腔作为一个相对封闭的液体空间,具备神经干细胞移植的基本条件,适宜移植细胞存活。但微环境中有关分子成分多促进神经干细胞向胶质细胞分化。

关键词: 脑梗死, 囊腔, 微环境, 脑脊液, 质谱分析, 差异因子

Abstract: Objective To study the liquefaction in the cystic cavity of cerebral infarction and the blood supply in the wall to explore whether it is suitable for neural stem cell transplantation. Methods A total of 20 male Sprague-Dawley rats were established middle cerebral artery occlusion (MCAO) model. They were observed the formation of cystic cavity three, ten and 21 days after modeling with MRI, and the coordinates of cystic cavity and lateral ventricle were recorded. Intracystic fluid and cerebrospinal fluid were extracted from the rats with cavities for mass spectrometry. Frozen sections of the brains were stained with HE and immunofluorescence agglutinin and observed. Results The cystic cavity in the infarction area became stable 21 days after modeling, which was composed of the brain tissue and the pia matter. There was no cellular structure in the center of the cystic cavity. The wall of the cystic cavity was partly composed of the pia matter. There were a large number of cells at the junction between the center of the cystic cavity and the meninges. Blood vessels distributed around the cystic cavity, similar with those in unaffected side. A total of 36 different molecules were screened out, in which 31 increased and five decreased. For the top ten molecules, most of them positively benefited stem cell transplantation, including anti-inflammatory, anti-tumor and promoting the survival of nerve cells. However, they did not liked to promote neural stem cells differentiating into neurons, but glial cells. Conclusion As a relatively closed fluid space, the cystic cavity formed in the chronic cerebral infarction can provide basic conditions for neural stem cell transplantation. However, relevant molecular components in the microenvironment mostly promote the differentiation of neural stem cells into glial cells.

Key words: cerebral infarction, cystic cavity, microenvironment, cerebrospinal fluid, mass spectrometry, differential factors

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