Journal: Journal of Molecular and Cellular Cardiology

Article Title: Angiotensin peptide synthesis and cyclic nucleotide modulation in sympathetic stellate ganglia

doi: 10.1016/j.yjmcc.2019.11.157

Figure Lengend Snippet: Highest abundant transcripts in young Wistar and preSHR stellate ganglia.

Article Snippet: Human stellate ganglia were shipped on dry ice in RNA later ® RNA Stabilization Solution (ThermoFisher).

Techniques: RNA Binding Assay, Binding Assay

Journal: Journal of Molecular and Cellular Cardiology

Article Title: Angiotensin peptide synthesis and cyclic nucleotide modulation in sympathetic stellate ganglia

doi: 10.1016/j.yjmcc.2019.11.157

Figure Lengend Snippet: Transcripts of angiotensin synthesizing genes were observed in the rat sympathetic stellate ganglia in the RNA-seq dataset. The transcriptome of the sympathetic stellate ganglia was sequenced using stellate ganglia extracted from four-week-old male Wistar rats ( n = 5) and age-matched male prehypertensive SHR (preSHR, n = 5). A KEGG analysis was carried out using the differentially expressed transcripts where the gene input was selected using the Benjamini-Hochburg p.adj < 0.05. The KEGG group ‘Renin Secretion’ was found to be significantly altered in the preSHR ganglia, where the gene input was selected using the Benjamini-Hochburg p.adj < 0.05 (a). A full list of the genes, the fold changes and respective levels of significance are reported in . The AngII and Ang1–7 synthesis pathways are outlined (b). Transcripts encoding the enzymes and precursors classically involved in the synthesis of AngII and Ang1–7 were identified in young rat stellate ganglia (b), where the relevant transcripts included Angiotensinogen ( Agt), Renin ( Ren ) and the Angiotensin Converting Enzymes ( Ace, Ace2 ). The transcripts for AngII receptors type 1 and 2 ( Agtr1a, Agtr1b, Agtr2) and for the Ang1–7 receptor Mas ( M as1 ) were also observed (c). Transcript abundances were not found to be differentially expressed in preSHR vs. Wistar ganglia, with the exception of Agtr1a that was significantly downregulated in the preSHR stellate ganglia (p. adj = 3.72 × 10 −8 , Salmon-DESeq2 method [ , ]).

Article Snippet: Human stellate ganglia were shipped on dry ice in RNA later ® RNA Stabilization Solution (ThermoFisher).

Techniques: RNA Sequencing Assay

Journal: Journal of Molecular and Cellular Cardiology

Article Title: Angiotensin peptide synthesis and cyclic nucleotide modulation in sympathetic stellate ganglia

doi: 10.1016/j.yjmcc.2019.11.157

Figure Lengend Snippet: Angiotensinergic mRNA transcript validation by qRT-PCR in rat stellate ganglia. The presence of the RNA transcripts Agt, Ren, Ace, Ace2, Agtr1a, Agtr1b, Agtr2 and Mas1 was confirmed by qRT-PCR in sympathetic stellate ganglia from four-week Wistar and preSHR ganglia (a), and 16-week adult Wistar and SHR (b). The qRT-PCR raw counts were first normalized to a control gene B2m as per the comparative (∆C T ) method . Each data point corresponds to one stellate RNA sample from one rat. Data are displayed as ∆C T mean ± SEM. FRET microscopy was conducted on sympathetic stellate neurons obtained from Wistar ( n = 11 rats, 3 cultures, 20 cells) and preSHR rats ( n = 9 rats, 3 cultures, 19 cells). Cells were transduced with the cGi500 FRET sensor and randomly selected for imaging. Increases in cGMP generation was observed in sympathetic neurons in response to Ang1–7 and AngII (c, d). Maximal FRET changes were evoked following administration of a combination of the NO-donor Sin-1 (10 μM) and the PDE inhibitor IBMX (100 μM). There was significantly greater cGMP generation in response to AngII in Wistar vs. preSHR neurons (two-way ANOVA, p = .0403). Peak FRET changes were obtained in response to AngII or Ang1–7 and converted to percentage FRET changes and values are depicted as a proportion of the maximal FRET change (%). There was no difference in peak FRET responses in response to Ang1–7 or between strains (d). Data are displayed as mean ± SEM.

Article Snippet: Human stellate ganglia were shipped on dry ice in RNA later ® RNA Stabilization Solution (ThermoFisher).

Techniques: Quantitative RT-PCR, Microscopy, Transduction, Imaging