Additional file 5 of Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia
Additional file 5: Supplementary Figure 5. Evidence of CAA pathology in AppSAA mice at 8 and 16 months of age. a Representative images of Aβ deposition in AppSAA +/+, AppSAA KI/+, and AppSAA KI/KI mice at 16 months of age; AppSAA KI/+ and AppSAA KI/KI exhibit parenchymal Aβ plaque deposition (exampl...
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creator | Xia, Dan Lianoglou, Steve Sandmann, Thomas Calvert, Meredith Suh, Jung H. Thomsen, Elliot Dugas, Jason Pizzo, Michelle E. DeVos, Sarah L. Earr, Timothy K. Lin, Chia-Ching Davis, Sonnet Ha, Connie Leung, Amy Wing-Sze Nguyen, Hoang Chau, Roni Yulyaningsih, Ernie Lopez, Isabel Solanoy, Hilda Masoud, Shababa T. Liang, Chun-chi Lin, Karin Astarita, Giuseppe Khoury, Nathalie Zuchero, Joy Yu Thorne, Robert G. Shen, Kevin Miller, Stephanie Palop, Jorge J. Garceau, Dylan Sasner, Michael Whitesell, Jennifer D. Harris, Julie A. Hummel, Selina Gnörich, Johannes Wind, Karin Kunze, Lea Zatcepin, Artem Brendel, Matthias Willem, Michael Haass, Christian Barnett, Daniel Zimmer, Till S. Orr, Anna G. Scearce-Levie, Kimberly Lewcock, Joseph W. Di Paolo, Gilbert Sanchez, Pascal E. |
description | Additional file 5: Supplementary Figure 5. Evidence of CAA pathology in AppSAA mice at 8 and 16 months of age. a Representative images of Aβ deposition in AppSAA +/+, AppSAA KI/+, and AppSAA KI/KI mice at 16 months of age; AppSAA KI/+ and AppSAA KI/KI exhibit parenchymal Aβ plaque deposition (examples indicated with yellow arrowheads for AppSAA KI/+) and Aβ deposition associated with leptomeningeal vessels (CAA; examples indicated with white arrows for both AppSAA KI/+ and AppSAA KI/KI). Scale bars = 1 mm. b Representative confocal images showing accumulation of Aβ surrounding leptomeningeal (pial) vessels (endothelial cells labeled by CD31 and smooth muscle cells labeled by alpha-smooth muscle actin, consistent with putative arteries/arterioles) in AppSAA mice at 8 and 16 months of age. Scale bars = 50 μm (left images and magnified views). c-e Super resolution confocal images from AppSAA KI/KI mice 16 months of age showing Aβ accumulation in a penetrating parenchymal vessel (c), branching leptomeningeal vessel in the ambient cistern (d) and a leptomeningeal vessel (e), scale bars = 20 μm for images across (c-e). |
doi_str_mv | 10.6084/m9.figshare.20056404 |
format | Image |
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Evidence of CAA pathology in AppSAA mice at 8 and 16 months of age. a Representative images of Aβ deposition in AppSAA +/+, AppSAA KI/+, and AppSAA KI/KI mice at 16 months of age; AppSAA KI/+ and AppSAA KI/KI exhibit parenchymal Aβ plaque deposition (examples indicated with yellow arrowheads for AppSAA KI/+) and Aβ deposition associated with leptomeningeal vessels (CAA; examples indicated with white arrows for both AppSAA KI/+ and AppSAA KI/KI). Scale bars = 1 mm. b Representative confocal images showing accumulation of Aβ surrounding leptomeningeal (pial) vessels (endothelial cells labeled by CD31 and smooth muscle cells labeled by alpha-smooth muscle actin, consistent with putative arteries/arterioles) in AppSAA mice at 8 and 16 months of age. Scale bars = 50 μm (left images and magnified views). c-e Super resolution confocal images from AppSAA KI/KI mice 16 months of age showing Aβ accumulation in a penetrating parenchymal vessel (c), branching leptomeningeal vessel in the ambient cistern (d) and a leptomeningeal vessel (e), scale bars = 20 μm for images across (c-e).</description><identifier>DOI: 10.6084/m9.figshare.20056404</identifier><language>eng</language><publisher>figshare</publisher><subject>Biochemistry ; Cancer ; Cell Biology ; FOS: Biological sciences ; FOS: Clinical medicine ; FOS: Health sciences ; Genetics ; Immunology ; Medicine ; Mental Health ; Neuroscience</subject><creationdate>2022</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-2620-5165</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,1888</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.20056404$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Xia, Dan</creatorcontrib><creatorcontrib>Lianoglou, Steve</creatorcontrib><creatorcontrib>Sandmann, Thomas</creatorcontrib><creatorcontrib>Calvert, Meredith</creatorcontrib><creatorcontrib>Suh, Jung H.</creatorcontrib><creatorcontrib>Thomsen, Elliot</creatorcontrib><creatorcontrib>Dugas, Jason</creatorcontrib><creatorcontrib>Pizzo, Michelle E.</creatorcontrib><creatorcontrib>DeVos, Sarah L.</creatorcontrib><creatorcontrib>Earr, Timothy K.</creatorcontrib><creatorcontrib>Lin, Chia-Ching</creatorcontrib><creatorcontrib>Davis, Sonnet</creatorcontrib><creatorcontrib>Ha, Connie</creatorcontrib><creatorcontrib>Leung, Amy Wing-Sze</creatorcontrib><creatorcontrib>Nguyen, Hoang</creatorcontrib><creatorcontrib>Chau, Roni</creatorcontrib><creatorcontrib>Yulyaningsih, Ernie</creatorcontrib><creatorcontrib>Lopez, Isabel</creatorcontrib><creatorcontrib>Solanoy, Hilda</creatorcontrib><creatorcontrib>Masoud, Shababa T.</creatorcontrib><creatorcontrib>Liang, Chun-chi</creatorcontrib><creatorcontrib>Lin, Karin</creatorcontrib><creatorcontrib>Astarita, Giuseppe</creatorcontrib><creatorcontrib>Khoury, Nathalie</creatorcontrib><creatorcontrib>Zuchero, Joy Yu</creatorcontrib><creatorcontrib>Thorne, Robert G.</creatorcontrib><creatorcontrib>Shen, Kevin</creatorcontrib><creatorcontrib>Miller, Stephanie</creatorcontrib><creatorcontrib>Palop, Jorge J.</creatorcontrib><creatorcontrib>Garceau, Dylan</creatorcontrib><creatorcontrib>Sasner, Michael</creatorcontrib><creatorcontrib>Whitesell, Jennifer D.</creatorcontrib><creatorcontrib>Harris, Julie A.</creatorcontrib><creatorcontrib>Hummel, Selina</creatorcontrib><creatorcontrib>Gnörich, Johannes</creatorcontrib><creatorcontrib>Wind, Karin</creatorcontrib><creatorcontrib>Kunze, Lea</creatorcontrib><creatorcontrib>Zatcepin, Artem</creatorcontrib><creatorcontrib>Brendel, Matthias</creatorcontrib><creatorcontrib>Willem, Michael</creatorcontrib><creatorcontrib>Haass, Christian</creatorcontrib><creatorcontrib>Barnett, Daniel</creatorcontrib><creatorcontrib>Zimmer, Till S.</creatorcontrib><creatorcontrib>Orr, Anna G.</creatorcontrib><creatorcontrib>Scearce-Levie, Kimberly</creatorcontrib><creatorcontrib>Lewcock, Joseph W.</creatorcontrib><creatorcontrib>Di Paolo, Gilbert</creatorcontrib><creatorcontrib>Sanchez, Pascal E.</creatorcontrib><title>Additional file 5 of Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia</title><description>Additional file 5: Supplementary Figure 5. Evidence of CAA pathology in AppSAA mice at 8 and 16 months of age. a Representative images of Aβ deposition in AppSAA +/+, AppSAA KI/+, and AppSAA KI/KI mice at 16 months of age; AppSAA KI/+ and AppSAA KI/KI exhibit parenchymal Aβ plaque deposition (examples indicated with yellow arrowheads for AppSAA KI/+) and Aβ deposition associated with leptomeningeal vessels (CAA; examples indicated with white arrows for both AppSAA KI/+ and AppSAA KI/KI). Scale bars = 1 mm. b Representative confocal images showing accumulation of Aβ surrounding leptomeningeal (pial) vessels (endothelial cells labeled by CD31 and smooth muscle cells labeled by alpha-smooth muscle actin, consistent with putative arteries/arterioles) in AppSAA mice at 8 and 16 months of age. Scale bars = 50 μm (left images and magnified views). c-e Super resolution confocal images from AppSAA KI/KI mice 16 months of age showing Aβ accumulation in a penetrating parenchymal vessel (c), branching leptomeningeal vessel in the ambient cistern (d) and a leptomeningeal vessel (e), scale bars = 20 μm for images across (c-e).</description><subject>Biochemistry</subject><subject>Cancer</subject><subject>Cell Biology</subject><subject>FOS: Biological sciences</subject><subject>FOS: Clinical medicine</subject><subject>FOS: Health sciences</subject><subject>Genetics</subject><subject>Immunology</subject><subject>Medicine</subject><subject>Mental 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Wing-Sze</creator><creator>Nguyen, Hoang</creator><creator>Chau, Roni</creator><creator>Yulyaningsih, Ernie</creator><creator>Lopez, Isabel</creator><creator>Solanoy, Hilda</creator><creator>Masoud, Shababa T.</creator><creator>Liang, Chun-chi</creator><creator>Lin, Karin</creator><creator>Astarita, Giuseppe</creator><creator>Khoury, Nathalie</creator><creator>Zuchero, Joy Yu</creator><creator>Thorne, Robert G.</creator><creator>Shen, Kevin</creator><creator>Miller, Stephanie</creator><creator>Palop, Jorge J.</creator><creator>Garceau, Dylan</creator><creator>Sasner, Michael</creator><creator>Whitesell, Jennifer D.</creator><creator>Harris, Julie A.</creator><creator>Hummel, Selina</creator><creator>Gnörich, Johannes</creator><creator>Wind, Karin</creator><creator>Kunze, Lea</creator><creator>Zatcepin, Artem</creator><creator>Brendel, Matthias</creator><creator>Willem, Michael</creator><creator>Haass, Christian</creator><creator>Barnett, Daniel</creator><creator>Zimmer, Till S.</creator><creator>Orr, Anna G.</creator><creator>Scearce-Levie, Kimberly</creator><creator>Lewcock, Joseph W.</creator><creator>Di Paolo, Gilbert</creator><creator>Sanchez, Pascal E.</creator><general>figshare</general><scope>DYCCY</scope><scope>PQ8</scope><orcidid>https://orcid.org/0000-0002-2620-5165</orcidid></search><sort><creationdate>20220612</creationdate><title>Additional file 5 of Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia</title><author>Xia, Dan ; Lianoglou, Steve ; Sandmann, Thomas ; Calvert, Meredith ; Suh, Jung H. ; Thomsen, Elliot ; Dugas, Jason ; Pizzo, Michelle E. ; DeVos, Sarah L. ; Earr, Timothy K. ; Lin, Chia-Ching ; Davis, Sonnet ; Ha, Connie ; Leung, Amy Wing-Sze ; Nguyen, Hoang ; Chau, Roni ; Yulyaningsih, Ernie ; Lopez, Isabel ; Solanoy, Hilda ; Masoud, Shababa T. ; Liang, Chun-chi ; Lin, Karin ; Astarita, Giuseppe ; Khoury, Nathalie ; Zuchero, Joy Yu ; Thorne, Robert G. ; Shen, Kevin ; Miller, Stephanie ; Palop, Jorge J. ; Garceau, Dylan ; Sasner, Michael ; Whitesell, Jennifer D. ; Harris, Julie A. ; Hummel, Selina ; Gnörich, Johannes ; Wind, Karin ; Kunze, Lea ; Zatcepin, Artem ; Brendel, Matthias ; Willem, Michael ; Haass, Christian ; Barnett, Daniel ; Zimmer, Till S. ; Orr, Anna G. ; Scearce-Levie, Kimberly ; Lewcock, Joseph W. ; Di Paolo, Gilbert ; Sanchez, Pascal E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_200564043</frbrgroupid><rsrctype>images</rsrctype><prefilter>images</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biochemistry</topic><topic>Cancer</topic><topic>Cell Biology</topic><topic>FOS: Biological sciences</topic><topic>FOS: Clinical medicine</topic><topic>FOS: Health sciences</topic><topic>Genetics</topic><topic>Immunology</topic><topic>Medicine</topic><topic>Mental 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Shababa T.</creatorcontrib><creatorcontrib>Liang, Chun-chi</creatorcontrib><creatorcontrib>Lin, Karin</creatorcontrib><creatorcontrib>Astarita, Giuseppe</creatorcontrib><creatorcontrib>Khoury, Nathalie</creatorcontrib><creatorcontrib>Zuchero, Joy Yu</creatorcontrib><creatorcontrib>Thorne, Robert G.</creatorcontrib><creatorcontrib>Shen, Kevin</creatorcontrib><creatorcontrib>Miller, Stephanie</creatorcontrib><creatorcontrib>Palop, Jorge J.</creatorcontrib><creatorcontrib>Garceau, Dylan</creatorcontrib><creatorcontrib>Sasner, Michael</creatorcontrib><creatorcontrib>Whitesell, Jennifer D.</creatorcontrib><creatorcontrib>Harris, Julie A.</creatorcontrib><creatorcontrib>Hummel, Selina</creatorcontrib><creatorcontrib>Gnörich, Johannes</creatorcontrib><creatorcontrib>Wind, Karin</creatorcontrib><creatorcontrib>Kunze, Lea</creatorcontrib><creatorcontrib>Zatcepin, Artem</creatorcontrib><creatorcontrib>Brendel, Matthias</creatorcontrib><creatorcontrib>Willem, Michael</creatorcontrib><creatorcontrib>Haass, Christian</creatorcontrib><creatorcontrib>Barnett, Daniel</creatorcontrib><creatorcontrib>Zimmer, Till S.</creatorcontrib><creatorcontrib>Orr, Anna G.</creatorcontrib><creatorcontrib>Scearce-Levie, Kimberly</creatorcontrib><creatorcontrib>Lewcock, Joseph W.</creatorcontrib><creatorcontrib>Di Paolo, Gilbert</creatorcontrib><creatorcontrib>Sanchez, Pascal E.</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Xia, Dan</au><au>Lianoglou, Steve</au><au>Sandmann, Thomas</au><au>Calvert, Meredith</au><au>Suh, Jung H.</au><au>Thomsen, Elliot</au><au>Dugas, Jason</au><au>Pizzo, Michelle E.</au><au>DeVos, Sarah L.</au><au>Earr, Timothy K.</au><au>Lin, Chia-Ching</au><au>Davis, Sonnet</au><au>Ha, Connie</au><au>Leung, Amy Wing-Sze</au><au>Nguyen, Hoang</au><au>Chau, Roni</au><au>Yulyaningsih, Ernie</au><au>Lopez, Isabel</au><au>Solanoy, Hilda</au><au>Masoud, Shababa T.</au><au>Liang, Chun-chi</au><au>Lin, Karin</au><au>Astarita, Giuseppe</au><au>Khoury, Nathalie</au><au>Zuchero, Joy Yu</au><au>Thorne, Robert G.</au><au>Shen, Kevin</au><au>Miller, Stephanie</au><au>Palop, Jorge J.</au><au>Garceau, Dylan</au><au>Sasner, Michael</au><au>Whitesell, Jennifer D.</au><au>Harris, Julie A.</au><au>Hummel, Selina</au><au>Gnörich, Johannes</au><au>Wind, Karin</au><au>Kunze, Lea</au><au>Zatcepin, Artem</au><au>Brendel, Matthias</au><au>Willem, Michael</au><au>Haass, Christian</au><au>Barnett, Daniel</au><au>Zimmer, Till S.</au><au>Orr, Anna G.</au><au>Scearce-Levie, Kimberly</au><au>Lewcock, Joseph W.</au><au>Di Paolo, Gilbert</au><au>Sanchez, Pascal E.</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><title>Additional file 5 of Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia</title><date>2022-06-12</date><risdate>2022</risdate><abstract>Additional file 5: Supplementary Figure 5. Evidence of CAA pathology in AppSAA mice at 8 and 16 months of age. a Representative images of Aβ deposition in AppSAA +/+, AppSAA KI/+, and AppSAA KI/KI mice at 16 months of age; AppSAA KI/+ and AppSAA KI/KI exhibit parenchymal Aβ plaque deposition (examples indicated with yellow arrowheads for AppSAA KI/+) and Aβ deposition associated with leptomeningeal vessels (CAA; examples indicated with white arrows for both AppSAA KI/+ and AppSAA KI/KI). Scale bars = 1 mm. b Representative confocal images showing accumulation of Aβ surrounding leptomeningeal (pial) vessels (endothelial cells labeled by CD31 and smooth muscle cells labeled by alpha-smooth muscle actin, consistent with putative arteries/arterioles) in AppSAA mice at 8 and 16 months of age. Scale bars = 50 μm (left images and magnified views). c-e Super resolution confocal images from AppSAA KI/KI mice 16 months of age showing Aβ accumulation in a penetrating parenchymal vessel (c), branching leptomeningeal vessel in the ambient cistern (d) and a leptomeningeal vessel (e), scale bars = 20 μm for images across (c-e).</abstract><pub>figshare</pub><doi>10.6084/m9.figshare.20056404</doi><orcidid>https://orcid.org/0000-0002-2620-5165</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biochemistry Cancer Cell Biology FOS: Biological sciences FOS: Clinical medicine FOS: Health sciences Genetics Immunology Medicine Mental Health Neuroscience |
title | Additional file 5 of Novel App knock-in mouse model shows key features of amyloid pathology and reveals profound metabolic dysregulation of microglia |
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