Journal: iScience

Article Title: Activation of limbal epithelial proliferation is partly controlled by the ACE2-LCN2 pathway

doi: 10.1016/j.isci.2024.110534

Figure Lengend Snippet:

Article Snippet: Rabbit anti-Ace2 , Proteintech , Cat:# 21115-1-AP; RRID: AB_10732845.

Techniques: Virus, Recombinant, Bicinchoninic Acid Protein Assay, RNA Sequencing, Software

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: Angiotensin synthesizing enzymes and precursors are expressed in human stellate ganglia. In human stellate ganglia the presence of the mRNA transcripts encoding Agt ( n = 4), Ren ( n = 3) , Ace (n = 4) , Ace2 (n = 3) , Agtr1 (n = 4) , Agtr2 (n = 3) and Mas1 (n = 4) were confirmed by qRT-PCR. The qRT-PCR raw counts for the genes of interest were normalized to the control gene B2m using the ∆C T method and expressed as ∆C T mean ± SEM (a). ELISAs were used to demonstrate the protein expression of the relevant proteins of interest including Agt, Ren, AngII, ACE2 and Ang1–7 in human stellate ganglia. Agt was found to be highly expressed in human stellate ganglia ( n = 2, ~53,694 pg/mg), as was Ren (n = 3, 2005 ± 388 pg/mg). AngII (n = 3, 188.7 ± 15.37 pg/mg), ACE2 (n = 2, 171.9 ± 2.60 pg/mg) and Ang1–7 (n = 3, 179.9 ± 6.13 pg/mg) were also identified and were found to have similar levels of expression (b). Data are displayed as mean ± SEM. A model diagram depicts AngII and Ang1–7 release from the stellate ganglia and the proposed pre-and post-synaptic effects.

Article Snippet: Two-step qRT-PCR was used to confirm the presence of the following mRNA transcripts in the stellate ganglia cDNA libraries: angiotensinogen (AGT, Agt; Rn00593114_m1, Hs01586213_m1; rat, human respectively), renin ( Ren ; Rn00561847_m1, Hs00982555_m1; rat, human), angiotensin converting enzyme (ACE, Ace, Rn00561094_m1, Hs00174179_m1; rat, human), angiotensin converting enzyme type 2 (ACE2, Ace2 ; Rn01416293_m1, Hs01085333_m1; rat, human), angiotensin II receptor subtype 1a (AT 1A R, Agtr1a ; Rn02758772_s1; rat), angiotensin II receptor subtype 1b (AT 1B R, Agtr1b ; Rn02132799_s1; rat), angiotensin II receptor type 1 (AT 1 R, Agtr1 ; Hs00258938_m1; human), angiotensin II receptor type 2 (AT 2 R, Agtr2 ; Rn00560677_s1, Hs02621316_s1; rat, human), Mas receptor (Mas R, Mas1 ; Rn00562673_s1, Hs00267157_s1; rat, human).

Techniques: Quantitative RT-PCR, Control, Expressing

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: Two-step qRT-PCR was used to confirm the presence of the following mRNA transcripts in the stellate ganglia cDNA libraries: angiotensinogen (AGT, Agt; Rn00593114_m1, Hs01586213_m1; rat, human respectively), renin ( Ren ; Rn00561847_m1, Hs00982555_m1; rat, human), angiotensin converting enzyme (ACE, Ace, Rn00561094_m1, Hs00174179_m1; rat, human), angiotensin converting enzyme type 2 (ACE2, Ace2 ; Rn01416293_m1, Hs01085333_m1; rat, human), angiotensin II receptor subtype 1a (AT 1A R, Agtr1a ; Rn02758772_s1; rat), angiotensin II receptor subtype 1b (AT 1B R, Agtr1b ; Rn02132799_s1; rat), angiotensin II receptor type 1 (AT 1 R, Agtr1 ; Hs00258938_m1; human), angiotensin II receptor type 2 (AT 2 R, Agtr2 ; Rn00560677_s1, Hs02621316_s1; rat, human), Mas receptor (Mas R, Mas1 ; Rn00562673_s1, Hs00267157_s1; rat, human).

Techniques: RNA Sequencing

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: Two-step qRT-PCR was used to confirm the presence of the following mRNA transcripts in the stellate ganglia cDNA libraries: angiotensinogen (AGT, Agt; Rn00593114_m1, Hs01586213_m1; rat, human respectively), renin ( Ren ; Rn00561847_m1, Hs00982555_m1; rat, human), angiotensin converting enzyme (ACE, Ace, Rn00561094_m1, Hs00174179_m1; rat, human), angiotensin converting enzyme type 2 (ACE2, Ace2 ; Rn01416293_m1, Hs01085333_m1; rat, human), angiotensin II receptor subtype 1a (AT 1A R, Agtr1a ; Rn02758772_s1; rat), angiotensin II receptor subtype 1b (AT 1B R, Agtr1b ; Rn02132799_s1; rat), angiotensin II receptor type 1 (AT 1 R, Agtr1 ; Hs00258938_m1; human), angiotensin II receptor type 2 (AT 2 R, Agtr2 ; Rn00560677_s1, Hs02621316_s1; rat, human), Mas receptor (Mas R, Mas1 ; Rn00562673_s1, Hs00267157_s1; rat, human).

Techniques: Biomarker Discovery, Quantitative RT-PCR, Control, Microscopy, Transduction, Imaging

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: Model diagram depicts angiotensin synthesis and pre- and post-synaptic signaling pathways. In sympathetic stellate neurons, the classical pathway for Angiotensin II (AngII) synthesis occurs by sequential enzymatic cleavage of Angiotensinogen (Agt) by renin and Angiotensin Converting Enzymes (ACE). AngII is hydrolyzed by ACE2 producing the bioactive metabolite of Angiotensin 1–7 (Ang1–7). We identified the presence of precursors and transcripts encoding these enzymes and depict here a proposed model for angiotensin synthesis (a). We also identified the presence of AngII and Ang1–7 receptors on sympathetic stellate ganglia of human and rat. AngII has been shown to elevate intracellular Ca 2+ and enhance noradrenaline release via actions at AT 1 R [ , ]. Conversely Ang1–7-dependent activation of its cognate receptor, Mas R, has been shown to couple to NO in the brain and several other receptor sites . In this study, we show that administration of both AngII and Ang1–7 elevate cGMP in the rat stellate ganglia. We and others have previously demonstrated the importance of NO-cGMP signaling in reducing [Ca 2+ ] i [ , ] and end-organ transmission in peripheral sympathetic stellate nerves [ , , , ] although the effects of Ang1–7 may be biphasic . Dotted lines indicate intermediates in these intracellular signaling pathway. Several effects of AngII and Ang1–7 on the myocardium have been established [ , , , , , ].

Article Snippet: Two-step qRT-PCR was used to confirm the presence of the following mRNA transcripts in the stellate ganglia cDNA libraries: angiotensinogen (AGT, Agt; Rn00593114_m1, Hs01586213_m1; rat, human respectively), renin ( Ren ; Rn00561847_m1, Hs00982555_m1; rat, human), angiotensin converting enzyme (ACE, Ace, Rn00561094_m1, Hs00174179_m1; rat, human), angiotensin converting enzyme type 2 (ACE2, Ace2 ; Rn01416293_m1, Hs01085333_m1; rat, human), angiotensin II receptor subtype 1a (AT 1A R, Agtr1a ; Rn02758772_s1; rat), angiotensin II receptor subtype 1b (AT 1B R, Agtr1b ; Rn02132799_s1; rat), angiotensin II receptor type 1 (AT 1 R, Agtr1 ; Hs00258938_m1; human), angiotensin II receptor type 2 (AT 2 R, Agtr2 ; Rn00560677_s1, Hs02621316_s1; rat, human), Mas receptor (Mas R, Mas1 ; Rn00562673_s1, Hs00267157_s1; rat, human).

Techniques: Protein-Protein interactions, Activation Assay, Transmission Assay

Journal: bioRxiv

Article Title: Human iPSC-derived alveolar and airway epithelial cells can be cultured at air-liquid interface and express SARS-CoV-2 host factors

doi: 10.1101/2020.06.03.132639

Figure Lengend Snippet: (A) Day 0 (undifferentiated RUES2 PSCs), RUES2 iAT2s cultured as 3D spheres, and primary adult HTII-280-sorted AT2s were profiled by RNA-Seq. iAT2s cultured as 3D spheres express ACE2 and TMPRSS2 at similar levels compared to primary adult AT2s. (B) Level of expression of ACE2 and TMPRSS2 in iAT2s cultured in 3D (iAT2 3D) and at ALI (iAT2 ALI), iBC-derived cells (iBasal, iCiliated, and iSecretory), and primary human lung cells (AT2, Proliferating Epithelial Cells, Transitional AT2, AT1, Basal, Ciliated, Secretory, KRT5-/KRT17+, Endothelial, Immune, Mesenchymal). (C) Percentage of cells expressing ACE2 and TMPRSS2 in iAT2s cultured in 3D (iAT2 3D) and at ALI (iAT2 ALI), iBC-derived cells (iBasal, iCiliated, and iSecretory), and primary human lung cells (AT2, Proliferating Epithelial Cells, Transitional AT2, AT1, Basal, Ciliated, Secretory, KRT5-/KRT17+, Endothelial, Immune, Mesenchymal).

Article Snippet: The iPSC line BU1CG was differentiated to human intestinal organoids (HIOs) and profiled by digital gene expression as previously described (Mithal 2020). qRT-PCR was performed using Taqman probes ACE2 (ThermoFisher Hs01085333_m1) and TMPRSS2 (ThermoFisher Hs01122322_m1).

Techniques: Cell Culture, RNA Sequencing, Expressing, Derivative Assay

Journal: bioRxiv

Article Title: Human iPSC-derived alveolar and airway epithelial cells can be cultured at air-liquid interface and express SARS-CoV-2 host factors

doi: 10.1101/2020.06.03.132639

Figure Lengend Snippet: (A) Log Counts Per Million (Log CPM) for ACE2 and TMPRSS2 of day 42 HIO compared to day 8 progenitors (n=2 replicates per condition, ****= p<0.0001 calculated as described . HIOs significantly upregulate ACE2 and TMPRSS2 compared to day 8 progenitors. (B) qRT-PCR of ACE2 and TMPRSS2 in undifferentiated day 0 iPSCs (n=1), day 30 HIOs (n=3 differentiations), and primary human adult colon (n=1). Fold change calculated as 2 -ΔΔCt over day 0 sample, error bars represent the s.d.

Article Snippet: The iPSC line BU1CG was differentiated to human intestinal organoids (HIOs) and profiled by digital gene expression as previously described (Mithal 2020). qRT-PCR was performed using Taqman probes ACE2 (ThermoFisher Hs01085333_m1) and TMPRSS2 (ThermoFisher Hs01122322_m1).

Techniques: Quantitative RT-PCR