Universidad de Murcia. Departamento de Biología Celular e Histología
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 sitespecificity 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