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NGF转基因小鼠免疫超神经支配的发育

Development of immune hyperinnervation in NGF-transgenic mice.

作者信息

Carlson S L, Johnson S, Parrish M E, Cass W A

机构信息

Department of Anatomy and Neurobiology, University of Kentucky Medical Center, Lexington 40536-0084, USA.

出版信息

Exp Neurol. 1998 Jan;149(1):209-20. doi: 10.1006/exnr.1997.6711.

Abstract

Sympathetic innervation of lymphoid tissues is localized to specific tissue compartments, but little is known of the "factors" that are important in establishing this pattern during development. Numerous studies have shown interactions of nerve growth factor (NGF) with the immune system, which may include modulation of immune innervation. We previously have shown that NGF transgenic mice, which overexpress NGF in skin and not immune tissues, have a dramatic hyperinnervation of splenic marginal zone and peripheral lymph node medulla and capsule. The purpose of the current studies was to determine if the presence of elevated NGF would alter immune system development and the process of sympathetic ingrowth. The results show that the splenic innervation in NGF transgenics gradually diverged from controls during the first two postnatal weeks, with the greatest change occurring between postnatal days 13 and 16 when the splenic organization was reaching the adult pattern. In contrast, the peripheral lymph nodes were hyperinnervated at an earlier age. mesenteric lymph nodes never diverged from the normal pattern. NGF levels in transgenic spleen were much higher than controls at postnatal days 1 and 2, when little innervation was present, and declined as the tissue matured, possibly because of NGF uptake by the ingrowing sympathetic fibers. This suggests that immune tissues are capable of concentrating NGF, which in turn may modulate the level of innervation by the sympathetic nervous system.

摘要

淋巴组织的交感神经支配定位于特定的组织区域,但对于在发育过程中建立这种模式起重要作用的“因子”却知之甚少。大量研究表明神经生长因子(NGF)与免疫系统存在相互作用,这可能包括对免疫神经支配的调节。我们之前已经表明,在皮肤而非免疫组织中过度表达NGF的NGF转基因小鼠,其脾脏边缘区以及外周淋巴结髓质和被膜有显著的神经支配过度。当前研究的目的是确定NGF水平升高是否会改变免疫系统发育以及交感神经长入的过程。结果显示,在出生后的前两周内,NGF转基因小鼠的脾脏神经支配逐渐与对照组出现差异,在出生后第13至16天,当脾脏组织达到成年模式时变化最为显著。相比之下,外周淋巴结在更早的年龄就出现了神经支配过度。肠系膜淋巴结从未偏离正常模式。在出生后第1天和第2天,当神经支配很少时,转基因脾脏中的NGF水平远高于对照组,并且随着组织成熟而下降,这可能是由于长入的交感神经纤维摄取了NGF。这表明免疫组织能够浓缩NGF,而NGF反过来可能调节交感神经系统的神经支配水平。

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