NEUROFILAMENT DEPENDENT STRUCTURING OF AXOPLASM

轴浆的神经丝依赖性结构

• 批准号: 7601046
• 负责人: Don W Cleveland
• 金额: $ 4.34万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-05-01 至 2008-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7601046
• 关键词: Axon; Caliber; Cells; Computer Retrieval of Information on Scientific Projects Database; Crush Injury; Cultured Cells; Data; Elderly; Fiber; Filament; Funding; Gene Targeting; Genetic; Grant; Growth; Insecta; Institution; Length; Life; Light; Microtubules; Mus; Mutation; Myelin; Neurofilament Proteins; Neurofilament-H; Neurofilament-M; Neurons; Phosphorylation; Phosphotransferases; Polymers; Protein Overexpression; Proteins; Quail; Radial; Ranvier' s Nodes; Rate; Recovery; Research; Research Personnel; Resources; Role; Schwann Cells; Signal Transduction; Source; Structure; Tail; United States National Institutes of Health; Yin; axon growth; axoplasm; insight; myelination; neurofilament; neuronal cell body; sciatic nerve; slow axonal transport

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Neurofilaments are the most abundant structural component of large myelinated axons, and are obligate hetero-polymers of neurofilament light (NF-L), medium (NF-M) and heavy (NF-H). As with most neuronal proteins, neurofilaments are synthesized in the soma, and are subsequently transported into the axon via slow axonal transport. Once in the axon, neurofilaments are extremely long-lived proteins involved in establishing and maintaining the three-dimensional array of axoplasm.Analysis of neurofilament expression following axonal recovery from crush injury suggested a role for neurofilaments in establishing axonal diameter (Hoffman et al., 1987). Genetics in both mouse and quail have unequivocally confirmed that neurofilaments are required for determining mature axonal diameter. In mouse, loss of neurofilaments (Elder et al., 1998; Eyer and Peterson, 1994; Jacomy et al., 1999; Ohara et al., 1993; Zhu et al., 1997) markedly suppresses the growth in axonal diameter that initiates during myelination. Moreover, axonal diameter is sensitive to the subunit ratio of neurofilaments as increased expression of any single subunit inhibits radial growth (Collard et al., 1995; Cote et al., 1993; Marszalek et al., 1996; Monteiro et al., 1990; Tu et al., 1995; Wong et al., 1995; Xu et al., 1996) whereas simultaneous overexpression of NF-L and NF-M or NF-H increases overall axonal diameter (Xu et al., 1996). Neurofilament dependent radial growth is itself associated with phosphorylation of the carboxy terminal tail domains of both NF-M and NF-H. Expression of full-length neurofilaments, and various truncation mutations, in Sf9 insect cells resulted in 10 nm fibers that formed carboxy terminal, phosphorylated cross-bridges that extended along the length of the filament (Chen et al., 2000; Nakagawa et al., 1995). Analysis of the sciatic nerve axoplasm suggested that these carboxy terminal cross-bridges contact adjacent neurofilaments and microtubules (Hirokawa et al., 1984; Rao et al., 2002). Furthermore, expression of carboxy terminally truncated NF-H resulted in mice with reduced rates of radial growth and markedly fewer cross-bridges. Interestingly, carboxy-terminal truncation of NF-H resulted in sub-regions of closely opposed neurofilaments that were not observed in wild type littermates (Rao et al., 2002). While neurofilaments and their phosphorylation are required for proper post-natal growth of axons, several lines of evidence suggests that neurofilament phosphorylation is regulated by myelinating cells (de Waegh et al., 1992; Yin et al., 1998). Axonal segments ensheathed by myelin defective Schwann cells do not undergo post-natal growth whereas segments of the same axon ensheathed by myelin-competent Schwann cells achieve large axonal diameters (de Waegh et al., 1992). These data strongly suggest that an outside-in signal cascade, originating from myelinating cells, activates local kinases or phosphotases (or both) resulting in increased local phosphorylation of the carboxy termini of NF-M and NF-H resulting in expansion of the axon (Hsieh et al., 1994). Moreover, neurofilaments that reside within the internode are nearly stoichoimetrically phosphorylated on the carboxy-terminal tail domain of NF-M and NF-H whereas NFs that reside in the Node of Ranvier are considerably less phosphorylated (Carden et al., 1985; Julien and Mushynski, 1983; Lee et al., 1988). Gene targeting and cell culture studies implicate NF-M as a possible target for a myelin-derived signal resulting in radial growth of axons (Elder et al., 1998). However, deletion of the entirety of NF-M does not offer insight into the specific sub-region(s) of NF-M targeted by a myelin-derived signal cascade.

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