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静脉注射骨髓基质细胞(MSCs)可增加大鼠创伤性脑损伤后脑内生长因子的表达。

Intravenous administration of marrow stromal cells (MSCs) increases the expression of growth factors in rat brain after traumatic brain injury.

作者信息

Mahmood Asim, Lu Dunyue, Chopp Michael

机构信息

Department of Neurosurgery and Neurology, Henry Ford Hospital, Detroit, Michigan 48020, USA.

出版信息

J Neurotrauma. 2004 Jan;21(1):33-9. doi: 10.1089/089771504772695922.

Abstract

This study was designed to investigate the effects of intravenous administration of marrow stromal cells (MSCs) on the expression of growth factors in rat brain after traumatic brain injury (TBI). The fate of transplanted MSCs and expression of growth factors was examined by immunohistochemistry. In addition, the level of growth factors was measured quantitatively using enzyme linked immunosorbent assay (ELISA). Growth factors that were studied included nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and basic fibroblast growth factor (bFGF). For immunohistochemical studies, 12 male Wistar rats were subjected to TBI and then divided into three groups with the first group receiving no treatment, the second group receiving saline (placebo) and the third group receiving MSCs intravenously 1 day after TBI. The neurological function of rats was studied by using Rotarod motor test and modified neurological severity scores. The animals were sacrificed 15 days after TBI and brain sections stained by immunohistochemistry to study the distribution of MSCs as well as expression of growth factors NGF, BDNF, and bFGF. For quantitative analysis, a second set of male Wistar rats (n = 18) was subjected to TBI and then injected with either saline (n = 9) or MSCs (n = 9) 1 day after injury. These rats were sacrificed on days 2, 5, and 8 after TBI and brain extracts used to measure NGF, BDNF, and bFGF. We found that after transplantation, MSCs preferentially migrated into the injured hemisphere and there was a statistically significant improvement in the functional outcome of MSC-treated rats compared to control rats. NGF, BDNF, and bFGF were expressed in the injured brain of both treated as well as control rats; however, quantitative ELISA studies showed that expression of NGF and BDNF was significantly increased (p < 0.05) in the treated group. This study shows that intravenous administration of MSCs after TBI increases the expression of growth factors (NGF, BDNF), which possibly contributes to the improvement in functional outcome seen in these rats.

摘要

本研究旨在探讨静脉注射骨髓基质细胞(MSCs)对创伤性脑损伤(TBI)大鼠脑内生长因子表达的影响。通过免疫组织化学检测移植的MSCs的命运以及生长因子的表达。此外,使用酶联免疫吸附测定(ELISA)定量测量生长因子的水平。所研究的生长因子包括神经生长因子(NGF)、脑源性神经营养因子(BDNF)和碱性成纤维细胞生长因子(bFGF)。对于免疫组织化学研究,12只雄性Wistar大鼠接受TBI,然后分为三组,第一组不接受治疗,第二组接受生理盐水(安慰剂),第三组在TBI后1天静脉注射MSCs。通过转棒运动试验和改良神经严重程度评分研究大鼠的神经功能。TBI后15天处死动物,脑切片进行免疫组织化学染色,以研究MSCs的分布以及生长因子NGF、BDNF和bFGF的表达。为了进行定量分析,第二组雄性Wistar大鼠(n = 18)接受TBI,然后在损伤后1天注射生理盐水(n = 9)或MSCs(n = 9)。这些大鼠在TBI后第2、5和8天处死,脑提取物用于测量NGF、BDNF和bFGF。我们发现,移植后,MSCs优先迁移到损伤的半球,与对照大鼠相比,接受MSCs治疗的大鼠的功能结局有统计学上的显著改善。NGF、BDNF和bFGF在治疗组和对照组大鼠的损伤脑中均有表达;然而,定量ELISA研究表明,治疗组中NGF和BDNF的表达显著增加(p < 0.05)。本研究表明,TBI后静脉注射MSCs可增加生长因子(NGF、BDNF)的表达,这可能有助于改善这些大鼠的功能结局。

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