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成熟脑和脊髓中蛋白聚糖的突触周围屏障

Perisynaptic barrier of proteoglycans in the mature brain and spinal cord.

作者信息

Murakami Takuro, Ohtsuka Aiji

机构信息

Department of Human Morphology, Functional Physiology, Biophysiological Science, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan.

出版信息

Arch Histol Cytol. 2003 Aug;66(3):195-207. doi: 10.1679/aohc.66.195.

DOI:10.1679/aohc.66.195
PMID:14527161
Abstract

Cell bodies and their dendrites of motor neurons, motor-related neurons, and certain other subsets of neurons such as GABAergic interneurons in the mature brain and spinal cord possess intensely negatively charged perineuronal or perisynaptic nets of proteoglycans which are linked to the nerve cell surface glycoproteins. These perineuronal nets of proteoglycans are digested by chondroitinase ABC, hyaluronidase, or collagenase, but not by endo-alpha-N-acetylgalactosaminidase, which is reactive to the nerve cell surface glycoproteins. Aggrecan, versican, neurocan, and brevican are members of a family of chondroitin sulfate proteoglycans that bind to hyaluronan. Neurocan- or brevican-deficient mice showed a regionally heterogeneous composition of proteoglycans in perineuronal nets. Aggrecan glycoforms contribute to the molecular heterogeneity of the perineuronal nets. Proteoglycans such as phosphacan are included in matrix-associated proteoglycans. The extracellular matrix glycoprotein tenascin-R is accumulated in the perineuronal nets. The perineuronal proteoglycans are produced by associated satellite astrocytes just before weaning, while the nerve cell surface glycoproteins are produced by the associated nerve cells at earlier stages after birth. The perineuronal proteoglycans may entrap the tissue fluid and form a perineuronal gel layer which protects the synapses as a "perisynaptic barrier". Degradation of the perineuronal proteoglycans or perisynaptic barrier by treatment with chondroitinase ABC or hyaluronidase reactivates the neuronal plasticity or promotes the functional recovery of a severed nervous system. Another set of perineuronal nets occurs, which are intensely positively charged and contain guanidino compounds. It is considered that these intensely positively charged nets are intermingled with the intensely negatively charged ones of proteoglycans.

摘要

成熟脑和脊髓中运动神经元、运动相关神经元以及某些其他神经元亚群(如GABA能中间神经元)的细胞体及其树突,具有与神经细胞表面糖蛋白相连的、带强负电荷的蛋白聚糖神经元周围或突触周围网络。这些蛋白聚糖神经元周围网络可被软骨素酶ABC、透明质酸酶或胶原酶消化,但不能被对神经细胞表面糖蛋白有反应的内切α-N-乙酰半乳糖胺酶消化。聚集蛋白聚糖、多功能蛋白聚糖、神经蛋白聚糖和短蛋白聚糖是与透明质酸结合的硫酸软骨素蛋白聚糖家族的成员。神经蛋白聚糖或短蛋白聚糖缺陷小鼠的神经元周围网络中蛋白聚糖的组成存在区域异质性。聚集蛋白聚糖糖型有助于神经元周围网络的分子异质性。诸如磷酸蛋白聚糖等蛋白聚糖包含在与基质相关的蛋白聚糖中。细胞外基质糖蛋白腱生蛋白-R在神经元周围网络中积累。神经元周围蛋白聚糖在断奶前由相关的卫星星形胶质细胞产生,而神经细胞表面糖蛋白在出生后的早期阶段由相关神经细胞产生。神经元周围蛋白聚糖可能会截留组织液并形成神经元周围凝胶层,作为“突触周围屏障”保护突触。用软骨素酶ABC或透明质酸酶处理使神经元周围蛋白聚糖或突触周围屏障降解,可重新激活神经元可塑性或促进受损神经系统的功能恢复。另一组神经元周围网络存在,其带强正电荷并含有胍基化合物。据认为,这些带强正电荷的网络与带强负电荷的蛋白聚糖网络相互交织。

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