Metallothionein-I/II Promotes Axonal Regeneration in the Central Nervous System. 2015

Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
From the Department of Biological Sciences, Hunter College, City University of New York, New York 10065 and mustafa.siddiq@mssm.edu.

The adult CNS does not spontaneously regenerate after injury, due in large part to myelin-associated inhibitors such as myelin-associated glycoprotein (MAG), Nogo-A, and oligodendrocyte-myelin glycoprotein. All three inhibitors can interact with either the Nogo receptor complex or paired immunoglobulin-like receptor B. A conditioning lesion of the sciatic nerve allows the central processes of dorsal root ganglion (DRG) neurons to spontaneously regenerate in vivo after a dorsal column lesion. After a conditioning lesion, DRG neurons are no longer inhibited by myelin, and this effect is cyclic AMP (cAMP)- and transcription-dependent. Using a microarray analysis, we identified several genes that are up-regulated both in adult DRGs after a conditioning lesion and in DRG neurons treated with cAMP analogues. One gene that was up-regulated under both conditions is metallothionein (MT)-I. We show here that treatment with two closely related isoforms of MT (MT-I/II) can overcome the inhibitory effects of both myelin and MAG for cortical, hippocampal, and DRG neurons. Intrathecal delivery of MT-I/II to adult DRGs also promotes neurite outgrowth in the presence of MAG. Adult DRGs from MT-I/II-deficient mice extend significantly shorter processes on MAG compared with wild-type DRG neurons, and regeneration of dorsal column axons does not occur after a conditioning lesion in MT-I/II-deficient mice. Furthermore, a single intravitreal injection of MT-I/II after optic nerve crush promotes axonal regeneration. Mechanistically, MT-I/II ability to overcome MAG-mediated inhibition is transcription-dependent, and MT-I/II can block the proteolytic activity of α-secretase and the activation of PKC and Rho in response to soluble MAG.

UI MeSH Term Description Entries
D008297 Male Males
D008668 Metallothionein A low-molecular-weight (approx. 10 kD) protein occurring in the cytoplasm of kidney cortex and liver. It is rich in cysteinyl residues and contains no aromatic amino acids. Metallothionein shows high affinity for bivalent heavy metals. Isometallothionein,Metallothionein A,Metallothionein B,Metallothionein I,Metallothionein II,Metallothionein IIA
D009186 Myelin Sheath The lipid-rich sheath surrounding AXONS in both the CENTRAL NERVOUS SYSTEMS and PERIPHERAL NERVOUS SYSTEM. The myelin sheath is an electrical insulator and allows faster and more energetically efficient conduction of impulses. The sheath is formed by the cell membranes of glial cells (SCHWANN CELLS in the peripheral and OLIGODENDROGLIA in the central nervous system). Deterioration of the sheath in DEMYELINATING DISEASES is a serious clinical problem. Myelin,Myelin Sheaths,Sheath, Myelin,Sheaths, Myelin
D009416 Nerve Regeneration Renewal or physiological repair of damaged nerve tissue. Nerve Tissue Regeneration,Nervous Tissue Regeneration,Neural Tissue Regeneration,Nerve Tissue Regenerations,Nervous Tissue Regenerations,Neural Tissue Regenerations,Regeneration, Nerve,Regeneration, Nerve Tissue,Regeneration, Nervous Tissue,Regeneration, Neural Tissue,Tissue Regeneration, Nerve,Tissue Regeneration, Nervous,Tissue Regeneration, Neural
D002490 Central Nervous System The main information-processing organs of the nervous system, consisting of the brain, spinal cord, and meninges. Cerebrospinal Axis,Axi, Cerebrospinal,Axis, Cerebrospinal,Central Nervous Systems,Cerebrospinal Axi,Nervous System, Central,Nervous Systems, Central,Systems, Central Nervous
D005260 Female Females
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001369 Axons Nerve fibers that are capable of rapidly conducting impulses away from the neuron cell body. Axon
D051381 Rats The common name for the genus Rattus. Rattus,Rats, Laboratory,Rats, Norway,Rattus norvegicus,Laboratory Rat,Laboratory Rats,Norway Rat,Norway Rats,Rat,Rat, Laboratory,Rat, Norway,norvegicus, Rattus
D018345 Mice, Knockout Strains of mice in which certain GENES of their GENOMES have been disrupted, or "knocked-out". To produce knockouts, using RECOMBINANT DNA technology, the normal DNA sequence of the gene being studied is altered to prevent synthesis of a normal gene product. Cloned cells in which this DNA alteration is successful are then injected into mouse EMBRYOS to produce chimeric mice. The chimeric mice are then bred to yield a strain in which all the cells of the mouse contain the disrupted gene. Knockout mice are used as EXPERIMENTAL ANIMAL MODELS for diseases (DISEASE MODELS, ANIMAL) and to clarify the functions of the genes. Knockout Mice,Mice, Knock-out,Mouse, Knockout,Knock-out Mice,Knockout Mouse,Mice, Knock out

Related Publications

Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
March 2021, Neurobiology of disease,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
February 1995, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
December 1974, Experimental neurology,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
May 2008, Neurotoxicology,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
April 2012, Journal of medicinal food,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
January 2022, Frontiers in neuroscience,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
February 2021, Cell death & disease,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
April 2023, PLoS biology,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
January 1990, Advances in anatomy, embryology, and cell biology,
Mustafa M Siddiq, and Sari S Hannila, and Jason B Carmel, and John B Bryson, and Jianwei Hou, and Elena Nikulina, and Matthew R Willis, and Wilfredo Mellado, and Erica L Richman, and Melissa Hilaire, and Ronald P Hart, and Marie T Filbin
April 2014, Nature communications,
Copied contents to your clipboard!