MicroRNA-24-3p regulates neuronal differentiation by controlling hippocalcin expression
Hippocalcin (HPCA) is a neuron-specific calcium-binding protein predominantly expressed in the nervous system. In the present study, we demonstrate that HPCA regulates neuronal differentiation in SH-SY5Y cells. We observed that the expression level of HPCA was increased during neuronal differentiati...
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Veröffentlicht in: | Cellular and molecular life sciences : CMLS 2019-11, Vol.76 (22), p.4569-4580 |
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Zusammenfassung: | Hippocalcin (HPCA) is a neuron-specific calcium-binding protein predominantly expressed in the nervous system. In the present study, we demonstrate that HPCA regulates neuronal differentiation in SH-SY5Y cells. We observed that the expression level of HPCA was increased during neuronal differentiation. Depletion of HPCA inhibited both neurite outgrowth and synaptophysin (SYP) expression, whereas overexpression of HPCA enhanced neuronal differentiation. Interestingly, we also found that the expression of
HPCA
mRNA was modulated by
miR
-
24
-
3p
. Using a dual-luciferase assay, we showed that co-transfection of a plasmid containing the
miR
-
24
-
3p
binding site from the 3′-untranslated region (3′UTR) of the
HPCA
gene and an
miR
-
24
-
3p
mimic effectively reduced luminescence activity. This effect was abolished when
miR
-
24
-
3p
seed sequences in the 3′UTR of the
HPCA
gene were mutated.
miR
-
24
-
3p
expression was decreased during differentiation, suggesting that the decreased expression level of
miR
-
24
-
3p
might have upregulated mRNA expression of
HPCA
. As expected, upregulation of
miR
-
24
-
3p
by an miRNA mimic led to reduced HPCA expression, accompanied by diminished neuronal differentiation. In contrast, downregulation of
miR
-
24
-
3p
by an antisense inhibitor promoted neurite outgrowth as well as levels of SYP expression. Taken together, these results suggest that
miR
-
24
-
3p
is an important miRNA that regulates neuronal differentiation by controlling HPCA expression. |
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ISSN: | 1420-682X 1420-9071 |
DOI: | 10.1007/s00018-019-03290-3 |