Aberrant hippocampal Atp8a1 levels are associated with altered synaptic strength, electrical activity, and autistic-like behavior
Autor: | Probal Banerjee, Silvia Menkes, Alexandra Marsillo, Guang Y. Wen, Abha Chauhan, Tatyana Budylin, Sara R. Guariglia, Andrzej Wieraszko, Rodina Sadek, Daniel P. McCloskey, Daniel J. Kerr |
---|---|
Rok vydání: | 2016 |
Předmět: |
Male
0301 basic medicine medicine.medical_specialty ATPase Hippocampus Hippocampal formation Temporal lobe Mice 03 medical and health sciences 0302 clinical medicine Microscopy Electron Transmission Internal medicine medicine Animals Humans Autistic Disorder Phospholipid Transfer Proteins Child Social Behavior CA1 Region Hippocampal Molecular Biology Adenosine Triphosphatases Mice Knockout Behavior Animal biology Flippase Temporal Lobe Mice Inbred C57BL Disease Models Animal 030104 developmental biology medicine.anatomical_structure Endocrinology Schaffer collateral Case-Control Studies Child Preschool Synapses biology.protein Excitatory postsynaptic potential Molecular Medicine 030217 neurology & neurosurgery Neurotypical |
Zdroj: | Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862:1755-1765 |
ISSN: | 0925-4439 |
DOI: | 10.1016/j.bbadis.2016.06.005 |
Popis: | Type IV ATPases are putative aminophospholipid translocases (APLTs), more commonly known as flippases. A pronounced induction of the flippase Atp8a1 was observed in post-mortem tissue homogenates from the hippocampus and temporal lobe of juvenile autistic subjects compared to age-matched controls. In order to simulate the human data, C57BL/6 mice were allowed to develop after intra-hippocampal injection of recombinant lentivirus expressing Atp8a1 at the early developmental stage of postnatal day 6 (P6). Transmission electron microscopy (TEM) analysis of the lentivirus-Atp8a1 treated (Atp8a1+) mice in adulthood revealed fewer and weaker excitatory synapses in the hippocampal CA1 region compared to mice injected with empty virus. Significant inhibition of the Schaffer collateral pathway was observed in the Atp8a1+ mice in paired-pulse recording (PPR) at 20-ms inter-stimulus interval. In the three-chambered sociability test, the Atp8a1+ mice displayed no preference for an encaged stranger mouse over a novel object, which is a characteristic autistic-like behavior. In sharp contrast, Atp8a1 (-/-) mice displayed a preference for a stranger mouse over the novel object, which is characteristic of neurotypical mouse behavior. However, similar to the Atp8a1+ mice, the Atp8a1 (-/-) mice harbored fewer and weaker excitatory synapses in CA1 compared to wild-type controls, and displayed inhibition at 20-ms inter-stimulus interval in PPR. These findings suggest that both elevated and diminished levels of Atp8a1 during early development are detrimental to brain connectivity, but only elevated Atp8a1 is associated with aberrant social behavior. Mice with augmented levels of Atp8a1 may therefore serve as a potential model in autism research. |
Databáze: | OpenAIRE |
Externí odkaz: |