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2.
Nat Methods ; 18(1): 46-49, 2021 01.
Article in English | MEDLINE | ID: mdl-33408404

ABSTRACT

We have developed a miniature two-photon microscope equipped with an axial scanning mechanism and a long-working-distance miniature objective to enable multi-plane imaging over a volume of 420 × 420 × 180 µm3 at a lateral resolution of ~1 µm. Together with the detachable design that permits long-term recurring imaging, our miniature two-photon microscope can help decipher neuronal mechanisms in freely behaving animals.


Subject(s)
Brain/diagnostic imaging , Brain/physiology , Microscopy, Fluorescence, Multiphoton/methods , Miniaturization/methods , Neuroimaging/methods , Animals , Behavior, Animal , Brain/cytology , Cytological Techniques , Locomotion , Male , Mice , Mice, Inbred C57BL
3.
J Neurooncol ; 129(2): 211-20, 2016 09.
Article in English | MEDLINE | ID: mdl-27294355

ABSTRACT

Gliomas are highly malignant tumors, the most common of which are astrocytomas. A growing number of studies suggest that dysregulation of miRNAs is a frequent event contributing to the pathogenesis of gliomas. In this study, we found that over-expression of miR-132 inhibited cell proliferation and migration and triggered apoptosis, while knockdown of miR-132 showed opposite effects. PEA-15 was identified as a direct target of miR-132. Reintroduction of PEA-15 without 3'UTR region reversed the inhibitory effects of miR-132 on cell proliferation, migration, and apoptosis. MiR-132 was inversely correlated with the PEA-15 expression. CREB (cAMP response element binding protein) and KLF (Krüppel-like factor 8) were conformed as transcription factors of miR-132, which bidirectionally regulate the expression of miR-132. Our study suggests that miR-132 is an important tumor suppressor of astrocytoma progression by targeting PEA-15, while CREB and KLF can modulate the expression of miR-132, thus providing new insight into the molecular mechanisms underlying astrocytoma progression in vitro.


Subject(s)
Astrocytoma/metabolism , Brain Neoplasms/metabolism , Gene Expression Regulation, Neoplastic/physiology , Intracellular Signaling Peptides and Proteins/metabolism , MicroRNAs/metabolism , Phosphoproteins/metabolism , Analysis of Variance , Apoptosis/genetics , Apoptosis/physiology , Apoptosis Regulatory Proteins , Astrocytoma/pathology , Brain Neoplasms/pathology , CREB-Binding Protein/genetics , CREB-Binding Protein/metabolism , Cell Line, Tumor , Cell Movement/genetics , Cell Movement/physiology , Cell Proliferation/genetics , Cell Proliferation/physiology , Disease Progression , Gene Expression Regulation, Neoplastic/genetics , Glioma , HEK293 Cells , Humans , Kruppel-Like Transcription Factors , MicroRNAs/genetics , RNA, Messenger , Repressor Proteins/genetics , Repressor Proteins/metabolism , Sincalide/metabolism , Time Factors , Transfection
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