Premium
Heterochrony of postnatal accumulation of nonphosphorylated heavy‐chain neurofilament by neurons of the cat dorsal lateral geniculate nucleus
Author(s) -
Mikhalkin Aleksandr,
Nikitiina,
Merkulyeva Natalia
Publication year - 2021
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.25028
Subject(s) - neurofilament , biology , geniculate , nucleus , lateral geniculate nucleus , heterochrony , anatomy , neuroscience , visual cortex , ontogeny , immunohistochemistry , endocrinology , immunology
Accumulation of the heavy‐chain neurofilaments reflects the maturation status of neuronal structures. The spatial distribution and postnatal developmental dynamic of neurons expressing nonphosphorylated heavy‐chain neurofilaments (labeled by SMI‐32 antibody) were analyzed in the dorsal lateral geniculate nucleus (LGNd) of the cat. Both interlaminar and intralaminar differences in the dynamic of SMI‐32 staining were observed. The following results were obtained: (a) Ascending dorsoventral gradient in the density of SMI‐32 immunopositive (SMI‐32(+)) neurons (the greatest neuronal density in layer Cm, the minor in the top sublayer of layer A). This gradient was most prominent at the earliest stages of postnatal development (1st–2nd weeks) and slowly flattened up to adulthood; (b) Layer A1 exhibits increases in SMI‐32‐positive cells earlier than layer A; (c) The general transient increment in the number and density of SMI‐32(+) neurons around 2–5 postnatal weeks. Since SMI‐32 antibody is considered to be a putative marker for Y cells forming a motion processing stream, we suggest that peculiarities of SMI‐32 staining at geniculate level could reflect the heterogeneity of Y cell subpopulations and the heterochrony of their postnatal maturation.