Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia

Whole mouse embryos at three developmental timepoints, embryonic (E) day E10.5, E14.5, and E18.5, were analyzed for Agpat4 mRNA expression. Primary cortical mouse cultures prepared from E18.5 mouse brains were used for immunohistochemistry. Our data show that Agpat4 is differentially expressed at three timepoints in murine embryogenesis and is immunodetectable in both neurons and glial cells derived from the developing mouse brain. This paper contains data related to research concurrently published in Bradley et al. (2015) [1].


Subject area
Biology More specific subject area

Lipid biochemistry
Type of data Figure, graph How data was acquired Confocal fluorescence microscopy for AGPAT4 localization, real time PCR (qPCR) and deltaCt analysis for Agpat4 gene expression.

Data format
Raw (primary neural culture), analyzed (qPCR) Experimental factors Mouse embryos were harvested at 3 developmental timepoints

Experimental features
Agpat4 expression was determined by qPCR and SEM analysis, AGPAT4 localization was determined by confocal fluorescence microscopy Data source location University of Waterloo, Waterloo, Ontario, Canada

Data accessibility
Data is provided within the article

Value of the data
These data show that AGPAT4 is variably expressed during murine embryogenesis, suggesting possible importance during fetal development.
These data show that AGPAT4 is immunodetectable in both cortical neurons and glial cells. These data are valuable to researchers interested in investigating phospholipid synthesis during murine embryogenesis.
These data are valuable to researchers interested in phospholipid synthesis in brain cells.

Data
Acylglycerophosphate acyltransferase/lysophosphatidic acid acyltransferase (AGPAT/LPAAT) proteins catalyze the second step in the de novo synthesis of glycerophospholipids and triacylglycerols [2]. Largely identified through sequence homology, eleven AGPATs have been found in mice and humans [3]. A previous report by our laboratory identified AGPAT4 as a mitochondrial lysophosphatidic acid acyltransferase that is most highly expressed in brain [1]. To determine if AGPAT4 protein is immunodetectable in neurons and/or in glia, we performed immunohistochemistry on mixed cultures of primary cortical cells derived from brains of E18.5 embryonic mice. Cells were grown on coverslips for 7 days in Neurobasal s medium with B27 supplementation to promote neuronal differentiation. Primary neurons were identified as cells expressing the neuron-specific intermediate filament NESTIN, or cells positively co-staining with the fluorescent green Nissl stain Neurotrace 500/525 s . Glial cells were identified as cells that were immunopositive for glial fibrillary acidic protein (GFAP). AGPAT4 showed a diffuse, punctate staining ( Fig. 1) and was found to colocalize in cells that were identified as positive for either Nissl stain or immunodetectable NESTIN, indicating the presence of this enzyme in primary cortical neurons (Fig. 1). AGPAT4 was also detected in cells that co-express GFAP, indicating that it is also found in glial cells (Fig. 1).
Embryogenesis is a time of rapid cellular and organellar growth, which supports organogenesis. Development of cell membranes for expansion of specialized structures such as the central nervous system requires phospholipid biosynthesis, which requires the function of AGPATs. To determine whether Agpat4 mRNA is regulated during embryogenesis, total RNA was isolated from mouse embryos on developmental days E10.5, E14.5, and E18.5, and analyzed by RT-qPCR for relative Agpat4 mRNA expression normalized to 18s expression by the delta Ct method (Fig. 2). Agpat4 was upregulated 3.7-fold at developmental day E14.5 as compared to day E10.5. Agpat4 mRNA levels then decreased to only 4% of developmental day 14.5 levels immediately prior to birth, on day E18.5.

Primary neural culture
Fetal mice at embryonic day E18.5 were decapitated in a cell culture dish on ice containing dissection media (HBSS with 30 mM HEPES, 0.6% w/v glucose, 2% w/v sucrose, final pH 7.4). Brains were dissected out and transferred to a 15 mL conical tube, washed 3 Â with ice-cold dissection media, and the cortex was separated then incubated with 2 mL of pre-warmed 0.25% trypsin-EDTA for 20 min at 37°C in a humidified cell culture incubator with 5% CO 2 . Post-incubation, cells were centrifuged at 1000g for 5 min, trypsin was removed, and samples were washed once with warm dissection media. Brain samples were then re-suspended by pipetting in 2 mL of warm plating media (DMEM/F12þ 10% horse serum þ 10% FBS þ1% penicillin-streptomycin) until a homogenous mixture was achieved. The homogenate was strained using a 100 μm nylon cell strainer into a 50 mL conical tube, and centrifuged at 1000g for 5 min at 4°C. The pellet, containing mixed cortical neurons and glial cells, was re-suspended in 2 mL of plating media, and cells were seeded onto glass coverslips pretreated with poly-D-lysine and incubated at 37°C with 5% CO 2 for 3 h. Once cells attached to the plate, 50% of plating media was removed and supplemented with feeding media (Neurobasal media þ1% B27 supplement) to support the differentiation of primary neurons.

Immunofluorescence
Primary embryonic neurons and glial cells were isolated and grown on coverslips pretreated with poly-D-lysine, then fixed with 4% paraformaldehyde for 10 min, washed with PBS, and permeabilized with 0.5% Triton X-100 for 5 min at room temperature. Cells were then washed with PBS and blocked with 5% goat IgG serum in PBS. After 1 h, blocking serum was removed, and cells were incubated at room temperature for an additional hour with rabbit anti-AGPAT4 antibody (Bioss, Woburn MA), diluted 1:100 in PBS, alone or in combination with mouse anti-GFAP (1:500 dilution) or mouse anti-NESTIN antibodies (1:500 dilution) (Cell Signaling, Danvers MA). Cells were then washed with PBS, and incubated for 1 h at room temperature with Alexa Fluor s 488-conjugated anti-mouse IgG (Cell Signaling, Danvers MA), or stained with Neurotrace s 500/525 Green Fluorescent Nissl Stain (1:100 dilution in PBS) for 20 min at room temperature according to the manufacturer's protocol (Life Technologies, Carlsbad CA). Cells were then washed repeatedly with 0.1% Triton X-100 in PBS followed by PBS alone, stained with DAPI (1 μg/mL) for 15 mi, and mounted on glass microscope slides using Prolong Antifade.

RNA extraction, reverse transcription (RT) PCR, and real time (q) PCR
Total RNA was isolated from whole mouse embryos at embryonic (E) days E10.5, E14.5, and E18.5 using TRIzol s Reagent and quantified using a Nanodrop 2000 Spectrophotometer (Thermo Scientific, Waltham MA). cDNA was synthesized from 2 μg of RNA by oligo(dT) priming using SuperScript II Reverse Transcriptase according to the manufacturer's protocol. Expression of Agpat4 mRNA was determined using 1 μL of cDNA with Taqman gene expression assays (Mm00509777_m1 for Agpat4 and Mm04277571_s1 for 18S) in a CFX-96 Connect Real Time PCR Detection System (BioRad, Hercules CA). Gene expression levels were normalized to 18S and quantified by the ΔΔCt method.

Statistical analysis
The data are expressed as mean 7S.E.M. Statistically significant differences between two groups were assessed by Student's t test. Significance is accepted at P o0.05.