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Deciphering perivascular macrophages and microglia in the retinal ganglion cell layers.
Jeon, Jehwi; Park, Yong Soo; Kim, Sang-Hoon; Kong, Eunji; Kim, Jay; Yang, Jee Myung; Lee, Joo Yong; Kim, You-Me; Kim, In-Beom; Kim, Pilhan.
Affiliation
  • Jeon J; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
  • Park YS; KI for Health Science and Technology (KIHST), Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
  • Kim SH; Department of Anatomy, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Kong E; Institute for Basic Science, Daejeon, Republic of Korea.
  • Kim J; Department of Neuroscience, Columbia University, New York, NY, United States.
  • Yang JM; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
  • Lee JY; Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Kim YM; Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Kim IB; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
  • Kim P; Department of Anatomy, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Front Cell Dev Biol ; 12: 1368021, 2024.
Article in En | MEDLINE | ID: mdl-38596358
ABSTRACT

Introduction:

The classically defined two retinal microglia layers are distributed in inner and outer plexiform layers. Although there are some reports that retinal microglia are also superficially located around the ganglion cell layer (GCL) in contact with the vitreous, there has been a lack of detailed descriptions and not fully understood yet.

Methods:

We visualized the microglial layers by using CX3CR1-GFP (C57BL6) transgenic mice with both healthy and disease conditions including NaIO3-induced retinal degeneration models and IRBP-induced auto-immune uveitis models.

Result:

We found the GCL microglia has two subsets; peripheral (pph) microglia located on the retinal parenchyma and BAM (CNS Border Associated Macrophage) which have a special stretched phenotype only located on the surface of large retinal veins. First, in the pph microglia subset, but not in BAM, Galectin-3 and LYVE1 are focally expressed. However, LYVE1 is specifically expressed in the amoeboid or transition forms, except the typical dendritic morphology in the pph microglia. Second, BAM is tightly attached to the surface of the retinal veins and has similar morphology patterns in both the healthy and disease conditions. CD86+ BAM has a longer process which vertically passes the proximal retinal veins. Our data helps decipher the basic anatomy and pathophysiology of the retinal microglia in the GCL.

Discussion:

Our data helps decipher the basic anatomy and pathophysiology of the retinal microglia in the GCL.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Cell Dev Biol Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Cell Dev Biol Year: 2024 Type: Article