In search for a gold-standard procedure to count motor neurons in the spinal cord
- PMID: 29537481
- DOI: 10.14670/HH-11-983
In search for a gold-standard procedure to count motor neurons in the spinal cord
Abstract
Counting motor neurons within the spinal cord and brainstem represents a seminal step to comprehend the anatomy and physiology of the final common pathway sourcing from the CNS. Motor neuron loss allows to assess the severity of motor neuron disorders while providing a tool to assess disease modifying effects. Counting motor neurons at first implies gold standard identification methods. In fact, motor neurons may occur within mixed nuclei housing a considerable amount of neurons other than motor neurons. In the present review, we analyse various approaches to count motor neurons emphasizing both the benefits and bias of each protocol. A special emphasis is placed on discussing automated stereology. When automated stereology does not take into account site-specificity and does not distinguish between heterogeneous neuronal populations, it may confound data making such a procedure a sort of "guide for the perplex". Thus, if on the one hand automated stereology improves our ability to quantify neuronal populations, it may also hide false positives/negatives in neuronal counts. For instance, classic staining for antigens such as SMI-32, SMN and ChAT, which are routinely considered to be specific for motor neurons, may also occur in other neuronal types of the spinal cord. Even site specificity within Lamina IX may be misleading due to neuronal populations having a size and shape typical of motor neurons. This is the case of spinal border cells, which often surpass the border of Lamina VII and intermingle with motor neurons of Lamina IX. The present article discusses the need to join automated stereology with a dedicated knowledge of each specific neuroanatomical setting.
Similar articles
-
Expression of glutamate receptor subtypes in the spinal cord of control and mnd mice, a model of motor neuron disorder.J Neurosci Res. 2002 Nov 15;70(4):553-60. doi: 10.1002/jnr.10420. J Neurosci Res. 2002. PMID: 12404509
-
Neurons other than motor neurons in motor neuron disease.Histol Histopathol. 2017 Nov;32(11):1115-1123. doi: 10.14670/HH-11-895. Epub 2017 Apr 11. Histol Histopathol. 2017. PMID: 28397197 Review.
-
TDP-43 in differential diagnosis of motor neuron disorders.Acta Neuropathol. 2007 Jul;114(1):71-9. doi: 10.1007/s00401-007-0234-5. Epub 2007 Jun 14. Acta Neuropathol. 2007. PMID: 17569066
-
Motor neuron disease: a primary disorder of corticomotoneurons?Muscle Nerve. 1995 Mar;18(3):314-8. doi: 10.1002/mus.880180308. Muscle Nerve. 1995. PMID: 7870109
-
Spinal cord: motor neuron diseases.Neurol Clin. 2013 Feb;31(1):219-39. doi: 10.1016/j.ncl.2012.09.014. Neurol Clin. 2013. PMID: 23186902 Review.
Cited by
-
A KO mouse model for the lncRNA Lhx1os produces motor neuron alterations and locomotor impairment.iScience. 2022 Dec 28;26(1):105891. doi: 10.1016/j.isci.2022.105891. eCollection 2023 Jan 20. iScience. 2022. PMID: 36647387 Free PMC article.
-
Methylmercury Causes Neurodegeneration and Downregulation of Myelin Basic Protein in the Spinal Cord of Offspring Rats after Maternal Exposure.Int J Mol Sci. 2022 Mar 29;23(7):3777. doi: 10.3390/ijms23073777. Int J Mol Sci. 2022. PMID: 35409136 Free PMC article.
-
Inhibition of Autophagy In Vivo Extends Methamphetamine Toxicity to Mesencephalic Cell Bodies.Pharmaceuticals (Basel). 2021 Sep 29;14(10):1003. doi: 10.3390/ph14101003. Pharmaceuticals (Basel). 2021. PMID: 34681227 Free PMC article.
-
Histopathological changes of the spinal cord and motor neuron dynamics in SOD1 Tg mice.J Toxicol Pathol. 2022 Jan;35(1):129-133. doi: 10.1293/tox.2021-0056. Epub 2021 Oct 1. J Toxicol Pathol. 2022. PMID: 35221507 Free PMC article.
-
Efficient cytoplasmic cell quantification using a semi-automated FIJI-based tool.Sci Rep. 2025 Jul 28;15(1):27509. doi: 10.1038/s41598-025-12144-x. Sci Rep. 2025. PMID: 40721622 Free PMC article.