» Articles » PMID: 8987787

A Transcription-dependent Switch Controls Competence of Adult Neurons for Distinct Modes of Axon Growth

Overview
Journal J Neurosci
Specialty Neurology
Date 1997 Jan 15
PMID 8987787
Citations 212
Authors
Affiliations
Soon will be listed here.
Abstract

Although maturing neurons undergo a precipitous decline in the expression of genes associated with developmental axon growth, structural changes in axon arbors occur in the adult nervous system under both normal and pathological conditions. Furthermore, some neurons support extensive regrowth of long axons after nerve injury. Analysis of adult dorsal root ganglion (DRG) neurons in culture now shows that competence for distinct types of axon growth depends on different patterns of gene expression. In the absence of ongoing transcription, newly isolated neurons can extend compact, highly branched arbors during the first day in culture. Neurons subjected to peripheral axon injury 2-7 d before plating support a distinct mode of growth characterized by rapid extension of long, sparsely branched axons. A transition from "arborizing" to "elongating" growth occurs in naive adult neurons after approximately 24 hr in culture but requires a discrete period of new transcription after removal of the ganglia from the intact animal. Thus, peripheral axotomy-by nerve crush or during removal of DRGs--induces a transcription-dependent change that alters the type of axon growth that can be executed by these adult neurons. This transition appears to be triggered, in large part, by interruption of retrogradely transported signals, because blocking axonal transport in vivo can elicit competence for elongating growth in many DRG neurons. In contrast to peripheral axotomy, interruption of the centrally projecting axons of DRG neurons in vivo leads to subsequent growth in vitro that is intermediate between "arborizing" and "elongating" growth. This suggests that the transition between these two modes of growth is a multistep process and that individual steps may be regulated separately. These observations together suggest that structural remodeling in the adult nervous system need not involve the same molecular apparatus as long axon growth during development and regeneration.

Citing Articles

Disruption of G3BP1 granules promotes mammalian CNS and PNS axon regeneration.

Sahoo P, Agrawal M, Hanovice N, Ward P, Desai M, Smith T Proc Natl Acad Sci U S A. 2025; 122(9):e2411811122.

PMID: 40014573 PMC: 11892601. DOI: 10.1073/pnas.2411811122.


KHSRP-mediated Decay of Axonally Localized Prenyl-Cdc42 mRNA Slows Nerve Regeneration.

Zdradzinski M, Vaughn L, Matoo S, Trumbull K, Loomis A, Thames E bioRxiv. 2025; .

PMID: 39975228 PMC: 11839134. DOI: 10.1101/2025.02.06.636857.


Plasticity of Mouse Dorsal Root Ganglion Neurons by Innate Immune Activation Is Influenced by Electrophysiological Activity.

Friedman T, Lamothe S, Maguire A, Hammond T, Tenorio G, Hilton B J Neurochem. 2024; 169(1):e16292.

PMID: 39725852 PMC: 11671441. DOI: 10.1111/jnc.16292.


Muscarinic acetylcholine type 1 receptor antagonism activates TRPM3 to augment mitochondrial function and drive axonal repair in adult sensory neurons.

Chauhan S, Smith D, Shariati-Ievari S, Srivastava A, Dhingra S, Aliani M Mol Metab. 2024; 92:102083.

PMID: 39694091 PMC: 11732569. DOI: 10.1016/j.molmet.2024.102083.


Neither injury induced macrophages within the nerve, nor the environment created by Wallerian degeneration is necessary for enhanced in vivo axon regeneration after peripheral nerve injury.

Talsma A, Niemi J, Zigmond R J Neuroinflammation. 2024; 21(1):134.

PMID: 38802868 PMC: 11131297. DOI: 10.1186/s12974-024-03132-5.


References
1.
Delree P, Ribbens C, Martin D, Rogister B, Lefebvre P, Rigo J . Plasticity of developing and adult dorsal root ganglion neurons as revealed in vitro. Brain Res Bull. 1993; 30(3-4):231-7. DOI: 10.1016/0361-9230(93)90249-b. View

2.
Hess D, Patterson S, Smith D, Skene J . Neuronal growth cone collapse and inhibition of protein fatty acylation by nitric oxide. Nature. 1993; 366(6455):562-5. DOI: 10.1038/366562a0. View

3.
Woolley C, McEwen B . Estradiol mediates fluctuation in hippocampal synapse density during the estrous cycle in the adult rat. J Neurosci. 1992; 12(7):2549-54. PMC: 6575846. View

4.
Bottenstein J, Sato G . Growth of a rat neuroblastoma cell line in serum-free supplemented medium. Proc Natl Acad Sci U S A. 1979; 76(1):514-7. PMC: 382972. DOI: 10.1073/pnas.76.1.514. View

5.
Verge V, Tetzlaff W, Richardson P, Bisby M . Correlation between GAP43 and nerve growth factor receptors in rat sensory neurons. J Neurosci. 1990; 10(3):926-34. PMC: 6570121. View