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胎儿下丘脑移植促进成年视上核大细胞神经元轴突切断后的存活和功能再生。

Fetal hypothalamic transplants promote survival and functional regeneration of axotomized adult supraoptic magnocellular neurons.

作者信息

Marciano F F, Wiegand S J, Sladek J R, Gash D M

机构信息

Department of Neurobiology and Anatomy, University of Rochester School of Medicine, NY 14642.

出版信息

Brain Res. 1989 Mar 27;483(1):135-42. doi: 10.1016/0006-8993(89)90044-9.

Abstract

This study investigated the mechanisms by which fetal hypothalamic transplants promote functional recovery in neurohypophysectomized rats. Seven days after neurohypophysectomy (resulting in urine osmolalities of about 800 mOsm), young adult male Long-Evans rats received either fetal hypothalamic grafts (n = 10) or sham transplants (n = 7). Recovery from the lesioned-induced diabetes insipidus was monitored for 6 months and then the transplant sites were evaluated by immunocytochemistry. Surviving host supraoptic magnocellular neurons and neurophysin-positive grafted neurons were counted and their formation of neurohemal contacts evaluated by retrograde transport of systemically injected horseradish peroxidase (HRP). There were significantly more surviving supraoptic magnocellular neurons in neurohypophysectomized animals with median eminence-placed grafts (2236 +/- 261 neurons/animal) than in animals with ectopic tissue grafts (895 +/- 142 neurons/animal) or sham implants (1052 +/- 92 neurons/animal). Almost all surviving host magnocellular neurons were labeled with retrogradely transported HRP while virtually none of the grafted neurophysin positive cells showed evidence of HRP uptake. The degree of functional recovery was directly correlated with the increased survival of host neurons. By 8 weeks post-transplantation, animals with median eminence-placed grafts had recovered from their diabetes insipidus and could concentrate their urine to within normal limits (2,120 +/- 110 mOsm). This recovery was stable for the remainder of the 6 month test period. In contrast, animals with ectopic grafts and sham transplants had permanent deficits in fluid regulation. Our results provide evidence for the long-term capacity of fetal neural tissue implants to rescue host neurons from the cell death that typically occurs in the mature central nervous system after axotomy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究调查了胎儿下丘脑移植促进去神经垂体大鼠功能恢复的机制。在去神经垂体术后7天(导致尿渗透压约为800 mOsm),成年雄性Long-Evans大鼠接受胎儿下丘脑移植(n = 10)或假手术移植(n = 7)。对损伤诱导的尿崩症恢复情况进行了6个月的监测,然后通过免疫细胞化学评估移植部位。计数存活的宿主视上大细胞神经元和神经垂体素阳性移植神经元,并通过全身注射辣根过氧化物酶(HRP)的逆行运输评估它们形成的神经血接触。与异位组织移植动物(895±142个神经元/动物)或假植入动物(1052±92个神经元/动物)相比,在正中隆起处移植的去神经垂体动物中存活的视上大细胞神经元明显更多(2236±261个神经元/动物)。几乎所有存活的宿主大细胞神经元都被逆行运输的HRP标记,而几乎没有移植的神经垂体素阳性细胞显示出摄取HRP的证据。功能恢复程度与宿主神经元存活率的增加直接相关。移植后8周,正中隆起处移植的动物已从尿崩症中恢复,其尿液可浓缩至正常范围内(2120±110 mOsm)。在6个月测试期的剩余时间里,这种恢复情况稳定。相比之下,异位移植和假手术移植的动物在液体调节方面存在永久性缺陷。我们的结果为胎儿神经组织植入物长期拯救宿主神经元免于轴突切断后成熟中枢神经系统中通常发生的细胞死亡提供了证据。(摘要截断于250字)

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