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gfrα2  (R&D Systems)


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    Structured Review

    R&D Systems gfrα2
    Temporal dynamics of <t>GFRα2</t> fiber innervation. (A-F) Representative images of PGP9.5 staining in the dermal-epidermal junction in male (A-C) and female (D-F) mice at various disease time points. (G) Quantification of GFRα2+ fiber crossings per mm of dermal–epidermal length. **** p < 0.0001, Two-way ANOVA, Tukey’s multiple comparisons test.
    Gfrα2, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 37 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gfr%CE%B12/Human%2FMouse+GFR+alpha-2%2FGDNF+R+alpha-2+Antibody/pmc12859467-42-39-40
    Average 94 stars, based on 37 article reviews
    gfrα2 - by Bioz Stars, 2026-11
    94/100 stars

    Images

    1) Product Images from "Peripheral immune response and axonal degeneration in the hind paw skin of mice with experimental autoimmune encephalomyelitis"

    Article Title: Peripheral immune response and axonal degeneration in the hind paw skin of mice with experimental autoimmune encephalomyelitis

    Journal: Neurobiology of Pain

    doi: 10.1016/j.ynpai.2025.100207

    Temporal dynamics of GFRα2 fiber innervation. (A-F) Representative images of PGP9.5 staining in the dermal-epidermal junction in male (A-C) and female (D-F) mice at various disease time points. (G) Quantification of GFRα2+ fiber crossings per mm of dermal–epidermal length. **** p < 0.0001, Two-way ANOVA, Tukey’s multiple comparisons test.
    Figure Legend Snippet: Temporal dynamics of GFRα2 fiber innervation. (A-F) Representative images of PGP9.5 staining in the dermal-epidermal junction in male (A-C) and female (D-F) mice at various disease time points. (G) Quantification of GFRα2+ fiber crossings per mm of dermal–epidermal length. **** p < 0.0001, Two-way ANOVA, Tukey’s multiple comparisons test.

    Techniques Used: Staining

    Related Articles

    Cell Culture:

    Article Title: Visceral motor neuron diversity delineates a cellular basis for nipple- and pilo-erection muscle control.
    Article Snippet: The visceral (or autonomic) motor system controls involuntary functions that are regulated by the activity of smooth muscle fibers, cardiac muscle fibers and glands.. The two major divisions include the sympathetic and parasympathetic systems.. The control of both divisions is modulated by inputs from the hypothalamus to preganglionic neurons in the brainstem and spinal cord, which in turn determine the activity of the primary visceral motor neurons in autonomic ganglia.

    Control:

    Article Title: Visceral motor neuron diversity delineates a cellular basis for nipple- and pilo-erection muscle control.
    Article Snippet: The visceral (or autonomic) motor system controls involuntary functions that are regulated by the activity of smooth muscle fibers, cardiac muscle fibers and glands.. The two major divisions include the sympathetic and parasympathetic systems.. The control of both divisions is modulated by inputs from the hypothalamus to preganglionic neurons in the brainstem and spinal cord, which in turn determine the activity of the primary visceral motor neurons in autonomic ganglia.

    Recombinant:

    Article Title: Genetic interplay between transcription factor Pou4f1/Brn3a and neurotrophin receptor Ret in retinal ganglion cell type specification
    Article Snippet: .. GFRα2 1:100 Anti- GFRα2 antibody (R&D Systems; AF429, RRID: AB_2294621) is a polyclonal goat antibody raised against NS0-derived recombinant mouse GFRα-2/GDNF Rα-2 (aminoacids Ser22-Ser441), and affinity purified with the target antigen. ..

    Affinity Purification:

    Article Title: Genetic interplay between transcription factor Pou4f1/Brn3a and neurotrophin receptor Ret in retinal ganglion cell type specification
    Article Snippet: .. GFRα2 1:100 Anti- GFRα2 antibody (R&D Systems; AF429, RRID: AB_2294621) is a polyclonal goat antibody raised against NS0-derived recombinant mouse GFRα-2/GDNF Rα-2 (aminoacids Ser22-Ser441), and affinity purified with the target antigen. ..

    Article Title: Peripheral injury of pelvic visceral sensory nerves alters GFRα (GDNF family receptor alpha) localization in sensory and autonomic pathways of the sacral spinal cord
    Article Snippet: .. Transverse sections were then incubated on a shaker (48 h at room temperature) in affinity purified antisera raised against goat GFRα1 (1:400; R&D Systems, Minneapolis, MN, cat. no. AF560; RRID:AB_2110307), GFRα2 (1:1000, R&D Systems, cat. no. AF429; RRID:AB_2294621), GFRα3 (1:300, R&D Systems, cat. no. AF2645; RRID:AB_2110295) or rabbit CGRP (1:2000, Millipore, Vic, Australia, cat. no. RRID:AB_2068655). ..

    Incubation:

    Article Title: Peripheral injury of pelvic visceral sensory nerves alters GFRα (GDNF family receptor alpha) localization in sensory and autonomic pathways of the sacral spinal cord
    Article Snippet: .. Transverse sections were then incubated on a shaker (48 h at room temperature) in affinity purified antisera raised against goat GFRα1 (1:400; R&D Systems, Minneapolis, MN, cat. no. AF560; RRID:AB_2110307), GFRα2 (1:1000, R&D Systems, cat. no. AF429; RRID:AB_2294621), GFRα3 (1:300, R&D Systems, cat. no. AF2645; RRID:AB_2110295) or rabbit CGRP (1:2000, Millipore, Vic, Australia, cat. no. RRID:AB_2068655). ..

    Article Title: Angiotensin II receptor type 2 activation is required for cutaneous sensory hyperinnervation and hypersensitivity in a rat hind paw model of inflammatory pain
    Article Snippet: Sections were immersed for 1 hour at room temperature in blocking solution containing 1.5% normal goat or donkey serum (Jackson ImmunoResearch Laboratories, Inc. West Grove, PA), 0.5% porcine gelatin (Sigma, St. Louis, MO), 0.5% Triton X-100 (Sigma), and SuperBlock in PBS (Thermo Scientific, Rockford, IL). .. Sections were incubated overnight at room temperature with primary antibodies directed against PGP9.5 (rabbit IgG,1:1200, AbD Serotec, Raleigh, NC), CGRP (sheep polyclonal, 1:500, Enzo Life Sciences International, Inc., Plymouth Meeting, PA), langerin (goat polyclonal, 1:100, Santa Cruz Biotechnology Inc., Santa Cruz, CA), GFRα2 (goat polyclonal, 1:800, R&D Systems, Inc., Minneapolis, MN), monoclonal anti- neurofilament 200 (mouse IgG1 isotype, 1:200, Sigma, St. Louis, MO), tyrosine hydroxylase (rabbit polyclonal, 1:200, EMD Millipore, Temecula, CA), renin (rabbit anti-rat antisera, 1:6000, a gift from Dr. T. Inagami, Vanderbilt University, Nashville, TN), angiotensinogen (rabbit monoclonal, 1:800; Swant, Bellinzona, Switzerland), TCR α/β, a T-cell marker (mouse monoclonal, 1:100, AbD Serotec, Raleigh, NC), and CD68 anti-macrophage/monocyte antibody (clone ED-1, mouse monoclonal, 1:100, EMD Millipore, Temecula, CA). .. Slides were rinsed with phosphate buffered saline containing 0.3% triton X-100 or 0.05% Tween-20 (Sigma), and incubated with Cy2 conjugated goat anti-rabbit (1:200; Jackson ImmunoResearch, West Grove, PA), Alexa 488 donkey anti sheep (1:800; Jackson), Cy3 conjugated donkey anti-rabbit (1:400, Jackson), Cy2 conjugated donkey anti-mouse (1:200, Jackson), Cy3 conjugated goat anti-mouse (1:200, Jackson), or Cy2 conjugated donkey anti-goat (1:200, Jackson) at room temperature for 1 h. Antibody specificity was confirmed by primary antisera preabsorption with blocking peptides, heat inactivation and antibody omissions.

    Immunohistochemistry:

    Article Title: GDNF availability determines enteric neuron number by controlling precursor proliferation.
    Article Snippet: Activated caspase 3 antibody (D175, Cell Signaling Technology, 1:100) staining was performed on 6 μm paraffin wax-embedded specimens. .. GFRα1 and GFRα2 (BAF560 and BAF429 respectively; R&D Systems, 1:40) immunohistochemistry was performed on 12 μm fresh frozen sections. ..

    Marker:

    Article Title: Angiotensin II receptor type 2 activation is required for cutaneous sensory hyperinnervation and hypersensitivity in a rat hind paw model of inflammatory pain
    Article Snippet: Sections were immersed for 1 hour at room temperature in blocking solution containing 1.5% normal goat or donkey serum (Jackson ImmunoResearch Laboratories, Inc. West Grove, PA), 0.5% porcine gelatin (Sigma, St. Louis, MO), 0.5% Triton X-100 (Sigma), and SuperBlock in PBS (Thermo Scientific, Rockford, IL). .. Sections were incubated overnight at room temperature with primary antibodies directed against PGP9.5 (rabbit IgG,1:1200, AbD Serotec, Raleigh, NC), CGRP (sheep polyclonal, 1:500, Enzo Life Sciences International, Inc., Plymouth Meeting, PA), langerin (goat polyclonal, 1:100, Santa Cruz Biotechnology Inc., Santa Cruz, CA), GFRα2 (goat polyclonal, 1:800, R&D Systems, Inc., Minneapolis, MN), monoclonal anti- neurofilament 200 (mouse IgG1 isotype, 1:200, Sigma, St. Louis, MO), tyrosine hydroxylase (rabbit polyclonal, 1:200, EMD Millipore, Temecula, CA), renin (rabbit anti-rat antisera, 1:6000, a gift from Dr. T. Inagami, Vanderbilt University, Nashville, TN), angiotensinogen (rabbit monoclonal, 1:800; Swant, Bellinzona, Switzerland), TCR α/β, a T-cell marker (mouse monoclonal, 1:100, AbD Serotec, Raleigh, NC), and CD68 anti-macrophage/monocyte antibody (clone ED-1, mouse monoclonal, 1:100, EMD Millipore, Temecula, CA). .. Slides were rinsed with phosphate buffered saline containing 0.3% triton X-100 or 0.05% Tween-20 (Sigma), and incubated with Cy2 conjugated goat anti-rabbit (1:200; Jackson ImmunoResearch, West Grove, PA), Alexa 488 donkey anti sheep (1:800; Jackson), Cy3 conjugated donkey anti-rabbit (1:400, Jackson), Cy2 conjugated donkey anti-mouse (1:200, Jackson), Cy3 conjugated goat anti-mouse (1:200, Jackson), or Cy2 conjugated donkey anti-goat (1:200, Jackson) at room temperature for 1 h. Antibody specificity was confirmed by primary antisera preabsorption with blocking peptides, heat inactivation and antibody omissions.



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    Temporal dynamics of <t>GFRα2</t> fiber innervation. (A-F) Representative images of PGP9.5 staining in the dermal-epidermal junction in male (A-C) and female (D-F) mice at various disease time points. (G) Quantification of GFRα2+ fiber crossings per mm of dermal–epidermal length. **** p < 0.0001, Two-way ANOVA, Tukey’s multiple comparisons test.
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    a , Cumulative time spent not responding to the tape (no-response time, seconds). b,c , Averaged time courses ± SEM of tape-directed bouts (b) and AUC (c) of CT (n = 8 M/7 F) and PS (n = 9 M/6 F) offspring. d , Ex vivo DRG neuron stimulation and calcium imaging. Percentage (%) of responsive neurons. e-g , Traces of the calcium-induced changes of fluorescence exclusively in responding neurons after addition of capsaicine (e, n = 35 [CT], 21 [PS]), b-alanine (f, n = 97 [CT], 57 [PS]) and MRS2365 (g, n = 87 [CT], 131 [PS]), and amplitude of the neuronal response measured as AUC of the highlighted duration (for 20 s after the addition of the stimulus), normalized per cell (upper panel) or per experiment (lower panel). Each triangle is a responding neuron, and each dot represents an experiment including 2 mice per group (d-g). h-j , Representative confocal microscopy images of neurofilament H (NFH, h) and GDNF Family Receptor Alpha 2 <t>(Gfrα2,</t> i) in glabrous skin sections and filament length (µm, j) per mm 2 in steady state W8 CT (n = 6) and PS (n = 7) offspring. Scale bars, 30 µm (cropped to 7 µm). k,l , Representative confocal microscopy images of Tubβ3, TH, IB4 and Substance P staining (k) and associated percentages (l) among all Tdt + neurons, in DRG from Nav1.8-Cre + ;Tdt CT (n = 6) and PS (n = 6 [TH + ], 7 [IB4 + , SP + ]) at steady state. Scale bars, 200 µm (cropped to 30 µm). Data are from at least two or three independent experiments. Bars represent mean values, and each dot or square corresponds to a single mouse (a,j,l). Mean + SEM; *P < 0.05, **P < 0.01, ***P < 0.001, ns: not significant; Unpaired t-test (a, c), Mann-Whitney test (d-g, j, l), two-sided. Illustrations in d were created using BioRender ( https://biorender.com ).
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    a , Cumulative time spent not responding to the tape (no-response time, seconds). b,c , Averaged time courses ± SEM of tape-directed bouts (b) and AUC (c) of CT (n = 8 M/7 F) and PS (n = 9 M/6 F) offspring. d , Ex vivo DRG neuron stimulation and calcium imaging. Percentage (%) of responsive neurons. e-g , Traces of the calcium-induced changes of fluorescence exclusively in responding neurons after addition of capsaicine (e, n = 35 [CT], 21 [PS]), b-alanine (f, n = 97 [CT], 57 [PS]) and MRS2365 (g, n = 87 [CT], 131 [PS]), and amplitude of the neuronal response measured as AUC of the highlighted duration (for 20 s after the addition of the stimulus), normalized per cell (upper panel) or per experiment (lower panel). Each triangle is a responding neuron, and each dot represents an experiment including 2 mice per group (d-g). h-j , Representative confocal microscopy images of neurofilament H (NFH, h) and GDNF Family Receptor Alpha 2 <t>(Gfrα2,</t> i) in glabrous skin sections and filament length (µm, j) per mm 2 in steady state W8 CT (n = 6) and PS (n = 7) offspring. Scale bars, 30 µm (cropped to 7 µm). k,l , Representative confocal microscopy images of Tubβ3, TH, IB4 and Substance P staining (k) and associated percentages (l) among all Tdt + neurons, in DRG from Nav1.8-Cre + ;Tdt CT (n = 6) and PS (n = 6 [TH + ], 7 [IB4 + , SP + ]) at steady state. Scale bars, 200 µm (cropped to 30 µm). Data are from at least two or three independent experiments. Bars represent mean values, and each dot or square corresponds to a single mouse (a,j,l). Mean + SEM; *P < 0.05, **P < 0.01, ***P < 0.001, ns: not significant; Unpaired t-test (a, c), Mann-Whitney test (d-g, j, l), two-sided. Illustrations in d were created using BioRender ( https://biorender.com ).
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    a , Cumulative time spent not responding to the tape (no-response time, seconds). b,c , Averaged time courses ± SEM of tape-directed bouts (b) and AUC (c) of CT (n = 8 M/7 F) and PS (n = 9 M/6 F) offspring. d , Ex vivo DRG neuron stimulation and calcium imaging. Percentage (%) of responsive neurons. e-g , Traces of the calcium-induced changes of fluorescence exclusively in responding neurons after addition of capsaicine (e, n = 35 [CT], 21 [PS]), b-alanine (f, n = 97 [CT], 57 [PS]) and MRS2365 (g, n = 87 [CT], 131 [PS]), and amplitude of the neuronal response measured as AUC of the highlighted duration (for 20 s after the addition of the stimulus), normalized per cell (upper panel) or per experiment (lower panel). Each triangle is a responding neuron, and each dot represents an experiment including 2 mice per group (d-g). h-j , Representative confocal microscopy images of neurofilament H (NFH, h) and GDNF Family Receptor Alpha 2 <t>(Gfrα2,</t> i) in glabrous skin sections and filament length (µm, j) per mm 2 in steady state W8 CT (n = 6) and PS (n = 7) offspring. Scale bars, 30 µm (cropped to 7 µm). k,l , Representative confocal microscopy images of Tubβ3, TH, IB4 and Substance P staining (k) and associated percentages (l) among all Tdt + neurons, in DRG from Nav1.8-Cre + ;Tdt CT (n = 6) and PS (n = 6 [TH + ], 7 [IB4 + , SP + ]) at steady state. Scale bars, 200 µm (cropped to 30 µm). Data are from at least two or three independent experiments. Bars represent mean values, and each dot or square corresponds to a single mouse (a,j,l). Mean + SEM; *P < 0.05, **P < 0.01, ***P < 0.001, ns: not significant; Unpaired t-test (a, c), Mann-Whitney test (d-g, j, l), two-sided. Illustrations in d were created using BioRender ( https://biorender.com ).
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    R&D Systems goat anti gfrα2
    a , Cumulative time spent not responding to the tape (no-response time, seconds). b,c , Averaged time courses ± SEM of tape-directed bouts (b) and AUC (c) of CT (n = 8 M/7 F) and PS (n = 9 M/6 F) offspring. d , Ex vivo DRG neuron stimulation and calcium imaging. Percentage (%) of responsive neurons. e-g , Traces of the calcium-induced changes of fluorescence exclusively in responding neurons after addition of capsaicine (e, n = 35 [CT], 21 [PS]), b-alanine (f, n = 97 [CT], 57 [PS]) and MRS2365 (g, n = 87 [CT], 131 [PS]), and amplitude of the neuronal response measured as AUC of the highlighted duration (for 20 s after the addition of the stimulus), normalized per cell (upper panel) or per experiment (lower panel). Each triangle is a responding neuron, and each dot represents an experiment including 2 mice per group (d-g). h-j , Representative confocal microscopy images of neurofilament H (NFH, h) and GDNF Family Receptor Alpha 2 <t>(Gfrα2,</t> i) in glabrous skin sections and filament length (µm, j) per mm 2 in steady state W8 CT (n = 6) and PS (n = 7) offspring. Scale bars, 30 µm (cropped to 7 µm). k,l , Representative confocal microscopy images of Tubβ3, TH, IB4 and Substance P staining (k) and associated percentages (l) among all Tdt + neurons, in DRG from Nav1.8-Cre + ;Tdt CT (n = 6) and PS (n = 6 [TH + ], 7 [IB4 + , SP + ]) at steady state. Scale bars, 200 µm (cropped to 30 µm). Data are from at least two or three independent experiments. Bars represent mean values, and each dot or square corresponds to a single mouse (a,j,l). Mean + SEM; *P < 0.05, **P < 0.01, ***P < 0.001, ns: not significant; Unpaired t-test (a, c), Mann-Whitney test (d-g, j, l), two-sided. Illustrations in d were created using BioRender ( https://biorender.com ).
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    Image Search Results


    Temporal dynamics of GFRα2 fiber innervation. (A-F) Representative images of PGP9.5 staining in the dermal-epidermal junction in male (A-C) and female (D-F) mice at various disease time points. (G) Quantification of GFRα2+ fiber crossings per mm of dermal–epidermal length. **** p < 0.0001, Two-way ANOVA, Tukey’s multiple comparisons test.

    Journal: Neurobiology of Pain

    Article Title: Peripheral immune response and axonal degeneration in the hind paw skin of mice with experimental autoimmune encephalomyelitis

    doi: 10.1016/j.ynpai.2025.100207

    Figure Lengend Snippet: Temporal dynamics of GFRα2 fiber innervation. (A-F) Representative images of PGP9.5 staining in the dermal-epidermal junction in male (A-C) and female (D-F) mice at various disease time points. (G) Quantification of GFRα2+ fiber crossings per mm of dermal–epidermal length. **** p < 0.0001, Two-way ANOVA, Tukey’s multiple comparisons test.

    Article Snippet: Primary antibodies included: CD45 (BD Biosciences 550539, 1:500), CD11b (Abcam ab133357, 1:200), CD11c (Abcam ab219799, 1:200), Ly6B.2 (Abcam ab53457, 1:200), CD4 (Abcam ab183685, 1:500), CD8 (Abcam ab217344, 1:500), PGP9.5 (EnCor Biotechnology 187–010116, 1:500), CGRP (Millipore Sigma PC205L-100UL, 1:500), and GFRα2 (R&D Systems AF429, 1:200).

    Techniques: Staining

    a , Cumulative time spent not responding to the tape (no-response time, seconds). b,c , Averaged time courses ± SEM of tape-directed bouts (b) and AUC (c) of CT (n = 8 M/7 F) and PS (n = 9 M/6 F) offspring. d , Ex vivo DRG neuron stimulation and calcium imaging. Percentage (%) of responsive neurons. e-g , Traces of the calcium-induced changes of fluorescence exclusively in responding neurons after addition of capsaicine (e, n = 35 [CT], 21 [PS]), b-alanine (f, n = 97 [CT], 57 [PS]) and MRS2365 (g, n = 87 [CT], 131 [PS]), and amplitude of the neuronal response measured as AUC of the highlighted duration (for 20 s after the addition of the stimulus), normalized per cell (upper panel) or per experiment (lower panel). Each triangle is a responding neuron, and each dot represents an experiment including 2 mice per group (d-g). h-j , Representative confocal microscopy images of neurofilament H (NFH, h) and GDNF Family Receptor Alpha 2 (Gfrα2, i) in glabrous skin sections and filament length (µm, j) per mm 2 in steady state W8 CT (n = 6) and PS (n = 7) offspring. Scale bars, 30 µm (cropped to 7 µm). k,l , Representative confocal microscopy images of Tubβ3, TH, IB4 and Substance P staining (k) and associated percentages (l) among all Tdt + neurons, in DRG from Nav1.8-Cre + ;Tdt CT (n = 6) and PS (n = 6 [TH + ], 7 [IB4 + , SP + ]) at steady state. Scale bars, 200 µm (cropped to 30 µm). Data are from at least two or three independent experiments. Bars represent mean values, and each dot or square corresponds to a single mouse (a,j,l). Mean + SEM; *P < 0.05, **P < 0.01, ***P < 0.001, ns: not significant; Unpaired t-test (a, c), Mann-Whitney test (d-g, j, l), two-sided. Illustrations in d were created using BioRender ( https://biorender.com ).

    Journal: Nature

    Article Title: Maternal stress triggers early-life eczema through fetal mast cell programming

    doi: 10.1038/s41586-025-09419-8

    Figure Lengend Snippet: a , Cumulative time spent not responding to the tape (no-response time, seconds). b,c , Averaged time courses ± SEM of tape-directed bouts (b) and AUC (c) of CT (n = 8 M/7 F) and PS (n = 9 M/6 F) offspring. d , Ex vivo DRG neuron stimulation and calcium imaging. Percentage (%) of responsive neurons. e-g , Traces of the calcium-induced changes of fluorescence exclusively in responding neurons after addition of capsaicine (e, n = 35 [CT], 21 [PS]), b-alanine (f, n = 97 [CT], 57 [PS]) and MRS2365 (g, n = 87 [CT], 131 [PS]), and amplitude of the neuronal response measured as AUC of the highlighted duration (for 20 s after the addition of the stimulus), normalized per cell (upper panel) or per experiment (lower panel). Each triangle is a responding neuron, and each dot represents an experiment including 2 mice per group (d-g). h-j , Representative confocal microscopy images of neurofilament H (NFH, h) and GDNF Family Receptor Alpha 2 (Gfrα2, i) in glabrous skin sections and filament length (µm, j) per mm 2 in steady state W8 CT (n = 6) and PS (n = 7) offspring. Scale bars, 30 µm (cropped to 7 µm). k,l , Representative confocal microscopy images of Tubβ3, TH, IB4 and Substance P staining (k) and associated percentages (l) among all Tdt + neurons, in DRG from Nav1.8-Cre + ;Tdt CT (n = 6) and PS (n = 6 [TH + ], 7 [IB4 + , SP + ]) at steady state. Scale bars, 200 µm (cropped to 30 µm). Data are from at least two or three independent experiments. Bars represent mean values, and each dot or square corresponds to a single mouse (a,j,l). Mean + SEM; *P < 0.05, **P < 0.01, ***P < 0.001, ns: not significant; Unpaired t-test (a, c), Mann-Whitney test (d-g, j, l), two-sided. Illustrations in d were created using BioRender ( https://biorender.com ).

    Article Snippet: Frozen or paraffin-embedded mouse skin sections pretreated using a heat-induced epitope retrieval method (in 10 mM sodium citrate buffer (pH 6.0)) were permeabilized for 30 min in PBS 0.5% (w/v)% BSA and 0.3% Triton X-100 and incubated overnight at 4 °C with fluorophore-coupled antibodies or unconjugated antibodies: anti-Filaggrin (Ozyme; BLE905801; 1:50), anti-Loricrin (Ozyme; BLE905101; 1:50), anti-mouse Keratin 6A (Ozyme; BLE905701; 1:50), Anti-Claudin 1 antibody (Abcam; ab15098; 1:50), Alexa Fluor 647 anti-mouse CD45 (BioLegend; 103124; 1:400), anti-TH (Sigma; AB1542; 1:100), Alexa Fluor 647 anti-Tubulin β3 (BioLegend; 801210; 1:50), anti-human/mouse GFRα2 (R&D Systems; AF429; 1:200), anti-mouse NFH (Sigma; AB1989; 1:1,000), anti-GFP (Proteintech; pabg1; 1:200), anti-RFP (Takara; 632496; 1:200), Anti-Substance P (Merck Millipore; MAB356; 1:200) and anti-αSMA (Thermo Fisher Scientific; 14-9760-82; Clone 1A4; 1/100).

    Techniques: Ex Vivo, Imaging, Fluorescence, Confocal Microscopy, Staining, MANN-WHITNEY