Requirement of heavy neurofilament subunit in the development of axons with large calibers

被引:116
作者
Elder, GA
Friedrich, VL
Kang, CH
Bosco, P
Gourov, A
Tu, PH
Zhang, B
Lee, VMY
Lazzarini, RA
机构
[1] CUNY, Mt Sinai Med Ctr, Brookdale Ctr Dev & Mol Biol, New York, NY 10029 USA
[2] CUNY, Mt Sinai Med Ctr, Dept Psychiat, New York, NY 10029 USA
[3] Univ Penn, Sch Med, Dept Pathol & Lab Med, Ctr Neurodegenerat Dis Res, Philadelphia, PA 19104 USA
关键词
neurofilament proteins; neuronal cytoskeleton; mice; knockout; gene targeting; large diameter axons;
D O I
10.1083/jcb.143.1.195
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neurofilaments (NFs) are prominent components of large myelinated axons. Previous studies have suggested that NF number as well as the phosphorylation state of the COOH-terminal tail of the heavy neurofilament (NF-H) subunit are major determinants of axonal caliber. We created NF-H knockout mice to assess the contribution of NF-H to the development of axon size as well as its effect on the amounts of low and mid-sized NF subunits (NF-L and NF-M respectively). Surprisingly, we found that NF-L levels were reduced only slightly whereas NF-M and tubulin proteins were unchanged in NF-H-null mice. However, the calibers of both large and small diameter myelinated axons were diminished in NF-H-null mice despite the fact that these mice showed only a slight decrease in NF density and that filaments in the mutant were most frequently spaced at the same interfilament distance found in control. Significantly, large diameter axons failed to develop in both the central and peripheral nervous systems. These results demonstrate directly that unlike losing the NF-L or NF-M subunits, loss of NF-H has only a slight effect on NF number in axons. Yet NF-H plays a major role in the development of large diameter axons.
引用
收藏
页码:195 / 205
页数:11
相关论文
共 62 条
  • [51] THE STRUCTURE OF THE LARGEST MURINE NEUROFILAMENT PROTEIN (NF-H) AS REVEALED BY CIS-DNA AND GENOMIC SEQUENCES
    SHNEIDMAN, PS
    CARDEN, MJ
    LEES, JF
    LAZZARINI, RA
    [J]. MOLECULAR BRAIN RESEARCH, 1988, 4 (03): : 217 - 231
  • [52] MOLECULAR AND CELLULAR BIOLOGY OF INTERMEDIATE FILAMENTS
    STEINERT, PM
    ROOP, DR
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1988, 57 : 593 - 625
  • [53] OVEREXPRESSION OF THE HUMAN NFM SUBUNIT IN TRANSGENIC MICE MODIFIES THE LEVEL OF ENDOGENOUS NFL AND THE PHOSPHORYLATION STATE OF NFH SUBUNITS
    TU, PH
    ELDER, G
    LAZZARINI, RA
    NELSON, D
    TROJANOWSKI, JQ
    LEE, VMY
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 129 (06) : 1629 - 1640
  • [54] A HIGH-MOLECULAR-WEIGHT SQUID NEUROFILAMENT PROTEIN CONTAINS A LAMIN-LIKE ROD DOMAIN AND A TAIL DOMAIN WITH LYS-SER-PRO REPEATS
    WAY, J
    HELLMICH, MR
    JAFFE, H
    SZARO, B
    PANT, HC
    GAINER, H
    BATTEY, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (15) : 6963 - 6967
  • [55] MODULATIONS OF NEUROFILAMENT AXONAL-TRANSPORT DURING THE DEVELOPMENT OF RABBIT RETINAL GANGLION-CELLS
    WILLARD, M
    SIMON, C
    [J]. CELL, 1983, 35 (02) : 551 - 559
  • [56] Wurst W., 1993, Gene targeting: a practical approach., P33
  • [57] Subunit composition of neurofilaments specifies axonal diameter
    Xu, ZS
    Marszalek, JR
    Lee, MK
    Wong, PC
    Folmer, J
    Crawford, TO
    Hsieh, ST
    Griffin, JW
    Cleveland, DW
    [J]. JOURNAL OF CELL BIOLOGY, 1996, 133 (05) : 1061 - 1069
  • [58] Xu Zuoshang, 1994, Current Opinion in Neurobiology, V4, P655, DOI 10.1016/0959-4388(94)90006-X
  • [59] HEREDITARY HYPOTROPHIC AXONOPATHY WITH NEUROFILAMENT DEFICIENCY IN A MUTANT STRAIN OF THE JAPANESE-QUAIL
    YAMASAKI, H
    ITAKURA, C
    MIZUTANI, M
    [J]. ACTA NEUROPATHOLOGICA, 1991, 82 (06) : 427 - 434
  • [60] Myelin-associated glycoprotein is a myelin signal that modulates the caliber of myelinated axons
    Yin, XH
    Crawford, TO
    Griffin, JW
    Tu, PH
    Lee, VMY
    Li, CM
    Roder, J
    Trapp, BD
    [J]. JOURNAL OF NEUROSCIENCE, 1998, 18 (06) : 1953 - 1962