Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2024 Sep 12;15:7998. doi: 10.1038/s41467-024-52396-1

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

PMC Copyright notice

Fig. 4 — Peripheral Aβ-binding monocytes (n ≥ 3, with a total of 22 blood samples analyzed) were analyzed using four-color immunophenotypic analysis. Aβ-binding monocytes exhibited a LIN-1⁺ and HLA-DR⁺ (MHC-II) phenotype (a, b), indicating differentiation from dendritic cells, and expressed CX3CR1 and CCR2 chemotactic receptors (c, d), suggesting strong migratory capabilities. They also showed CD68⁺ macrophage-like (e) and TREM2⁺ microglia-like phenotypes (f). Aβ-binding monocytes expressed Aβ-binding receptors (CD85A, CD85D, CD91) (g–i), complement receptors (CD11b, CD11c, CD35) (j–l), and phagocytosis-associated receptors (MerTK, P2X7R, CD163, CD33) (m–p). It is worth noting that in the four-color panel for TREM2 (f), what matches TREM2, CD14, and CD16 was Qdot525 conjugated W0-2, unlike in the other panels where W0-2 was used in conjunction with a secondary antibody.