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Immunohistochemical staining of the neocortex of control brain for <t>TG1,</t> TG2 and TG‐catalyzed cross‐links. The anti‐TG1 antibody stained both neurons in the gray matter (A, arrow) and glial cells in the white matter (B, arrow). TG1 immunoreactivity was absent in vessels of the neocortex (C, arrow). TG2 was present in neurons in the gray matter (D, arrow) and in glial cells in the white matter (E, arrow). TG2 staining was observed in both capillaries and parenchymal vessels (F, arrow). The anti‐TG‐catalyzed cross‐link antibody (anti‐CL) was immunoreactive in astrocytes of both the white and the gray matter (G, arrow) and in the nucleus of glial cells and neurons of the neocortex (H, arrow). Weak immunoreactivity of the anti‐CL antibody was observed in parenchymal vessels (I, arrow). Original magnification: A, C, D, F, G, I×200; B, E, H×150. Abbreviations: TG = transglutaminase; TG1 = transglutaminase 1; TG2 = transglutaminase 2.
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Immunohistochemical staining of the neocortex of control brain for <t>TG1,</t> TG2 and TG‐catalyzed cross‐links. The anti‐TG1 antibody stained both neurons in the gray matter (A, arrow) and glial cells in the white matter (B, arrow). TG1 immunoreactivity was absent in vessels of the neocortex (C, arrow). TG2 was present in neurons in the gray matter (D, arrow) and in glial cells in the white matter (E, arrow). TG2 staining was observed in both capillaries and parenchymal vessels (F, arrow). The anti‐TG‐catalyzed cross‐link antibody (anti‐CL) was immunoreactive in astrocytes of both the white and the gray matter (G, arrow) and in the nucleus of glial cells and neurons of the neocortex (H, arrow). Weak immunoreactivity of the anti‐CL antibody was observed in parenchymal vessels (I, arrow). Original magnification: A, C, D, F, G, I×200; B, E, H×150. Abbreviations: TG = transglutaminase; TG1 = transglutaminase 1; TG2 = transglutaminase 2.
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Immunohistochemical staining of the neocortex of control brain for TG1, TG2 and TG‐catalyzed cross‐links. The anti‐TG1 antibody stained both neurons in the gray matter (A, arrow) and glial cells in the white matter (B, arrow). TG1 immunoreactivity was absent in vessels of the neocortex (C, arrow). TG2 was present in neurons in the gray matter (D, arrow) and in glial cells in the white matter (E, arrow). TG2 staining was observed in both capillaries and parenchymal vessels (F, arrow). The anti‐TG‐catalyzed cross‐link antibody (anti‐CL) was immunoreactive in astrocytes of both the white and the gray matter (G, arrow) and in the nucleus of glial cells and neurons of the neocortex (H, arrow). Weak immunoreactivity of the anti‐CL antibody was observed in parenchymal vessels (I, arrow). Original magnification: A, C, D, F, G, I×200; B, E, H×150. Abbreviations: TG = transglutaminase; TG1 = transglutaminase 1; TG2 = transglutaminase 2.

Journal: Brain Pathology

Article Title: Transglutaminases and Transglutaminase‐Catalyzed Cross‐Links Colocalize with the Pathological Lesions in Alzheimer's Disease Brain

doi: 10.1111/j.1750-3639.2008.00197.x

Figure Lengend Snippet: Immunohistochemical staining of the neocortex of control brain for TG1, TG2 and TG‐catalyzed cross‐links. The anti‐TG1 antibody stained both neurons in the gray matter (A, arrow) and glial cells in the white matter (B, arrow). TG1 immunoreactivity was absent in vessels of the neocortex (C, arrow). TG2 was present in neurons in the gray matter (D, arrow) and in glial cells in the white matter (E, arrow). TG2 staining was observed in both capillaries and parenchymal vessels (F, arrow). The anti‐TG‐catalyzed cross‐link antibody (anti‐CL) was immunoreactive in astrocytes of both the white and the gray matter (G, arrow) and in the nucleus of glial cells and neurons of the neocortex (H, arrow). Weak immunoreactivity of the anti‐CL antibody was observed in parenchymal vessels (I, arrow). Original magnification: A, C, D, F, G, I×200; B, E, H×150. Abbreviations: TG = transglutaminase; TG1 = transglutaminase 1; TG2 = transglutaminase 2.

Article Snippet: Goat anti‐human TG1 (Sc‐18129, 1:100 dilution), C‐terminal part, was purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA).

Techniques: Immunohistochemical staining, Staining

Immunohistochemical staining for TG1 of SPs, CAA and NFTs in the neocortex of Alzheimer's disease brain. Serial sections: A–B, C–D, E–F, J–K. The anti‐Aβ antibody stained both classic (A, arrow) and diffuse SPs (C, arrow), and CAA (C, large arrow). The anti‐TG1 antibody was absent in both classic (B, arrow) and diffuse (D, arrow) SPs, and in CAA (D, large arrow). The anti‐tau antibody‐stained NFTs (E, arrow). Anti‐TG1 immunoreactivity was demonstrated in NFTs (F, arrow). Double immunofluorescence staining demonstrated colocalization of TG1 with hyperphosphorylated tau in NFTs (G–I). Specificity of the anti‐TG1 antibody was demonstrated by preadsorption of the antibody with human recombinant TG1 (J,K). Staining of NFTs with anti‐TG1 (J) is absent after preadsorption (K). Original magnification: A–F, J, K×200; G–I×400. Abbreviations: TG1 = transglutaminase 1; SPs = senile plaques; CAA = cerebral amyloid angiopathy; NFTs = neurofibrillary tangles; Aβ = amyloid‐β.

Journal: Brain Pathology

Article Title: Transglutaminases and Transglutaminase‐Catalyzed Cross‐Links Colocalize with the Pathological Lesions in Alzheimer's Disease Brain

doi: 10.1111/j.1750-3639.2008.00197.x

Figure Lengend Snippet: Immunohistochemical staining for TG1 of SPs, CAA and NFTs in the neocortex of Alzheimer's disease brain. Serial sections: A–B, C–D, E–F, J–K. The anti‐Aβ antibody stained both classic (A, arrow) and diffuse SPs (C, arrow), and CAA (C, large arrow). The anti‐TG1 antibody was absent in both classic (B, arrow) and diffuse (D, arrow) SPs, and in CAA (D, large arrow). The anti‐tau antibody‐stained NFTs (E, arrow). Anti‐TG1 immunoreactivity was demonstrated in NFTs (F, arrow). Double immunofluorescence staining demonstrated colocalization of TG1 with hyperphosphorylated tau in NFTs (G–I). Specificity of the anti‐TG1 antibody was demonstrated by preadsorption of the antibody with human recombinant TG1 (J,K). Staining of NFTs with anti‐TG1 (J) is absent after preadsorption (K). Original magnification: A–F, J, K×200; G–I×400. Abbreviations: TG1 = transglutaminase 1; SPs = senile plaques; CAA = cerebral amyloid angiopathy; NFTs = neurofibrillary tangles; Aβ = amyloid‐β.

Article Snippet: Goat anti‐human TG1 (Sc‐18129, 1:100 dilution), C‐terminal part, was purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA).

Techniques: Immunohistochemical staining, Staining, Double Immunofluorescence Staining, Recombinant

Summary of the percentage [mean (SD)] of NFTs, diffuse SPs, classic SPs or Aβ‐affected vessels that were stained for TG1, TG2 or TG‐catalyzed cross‐links. Abbreviations: NFTs = neurofibrillary tangles; SPs = senile plaques; CAA = cerebral amyloid angiopathy; SD = standard deviation; TG = transglutaminase; TG1 = transglutaminase 1; TG2 = transglutaminase 2.

Journal: Brain Pathology

Article Title: Transglutaminases and Transglutaminase‐Catalyzed Cross‐Links Colocalize with the Pathological Lesions in Alzheimer's Disease Brain

doi: 10.1111/j.1750-3639.2008.00197.x

Figure Lengend Snippet: Summary of the percentage [mean (SD)] of NFTs, diffuse SPs, classic SPs or Aβ‐affected vessels that were stained for TG1, TG2 or TG‐catalyzed cross‐links. Abbreviations: NFTs = neurofibrillary tangles; SPs = senile plaques; CAA = cerebral amyloid angiopathy; SD = standard deviation; TG = transglutaminase; TG1 = transglutaminase 1; TG2 = transglutaminase 2.

Article Snippet: Goat anti‐human TG1 (Sc‐18129, 1:100 dilution), C‐terminal part, was purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA).

Techniques: Staining, Standard Deviation