Anti-Inflammatory and Anti-(Lymph)angiogenic Properties of an ABCB5+ Limbal Mesenchymal Stem Cell Population

Author:

Meshko Berbang1ORCID,Volatier Thomas L. A.1ORCID,Mann Johanna1ORCID,Kluth Mark A.2ORCID,Ganss Christoph2,Frank Markus H.3456ORCID,Frank Natasha Y.578,Ksander Bruce R.9,Cursiefen Claus11011ORCID,Notara Maria11011

Affiliation:

1. Department of Ophthalmology, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany

2. RHEACELL GmbH & Co. KG, Im Neuenheimer Feld 517, 69120 Heidelberg, Germany

3. Transplant Research Program, Boston Children’s Hospital, Boston, MA 02115, USA

4. Harvard Skin Disease Research Center, Department of Dermatology, Brigham and Women’s Hospital, Boston, MA 02115, USA

5. Harvard Stem Cell Institute, Harvard University, Cambridge, MA 02138, USA

6. School of Medical and Health Sciences, Edith Cowan University, Perth, WA 6027, Australia

7. Department of Medicine, VA Boston Healthcare System, Boston, MA 02132, USA

8. Division of Genetics, Brigham and Women’s Hospital, Boston, MA 02115, USA

9. Massachusetts Eye & Ear Infirmary, Schepens Eye Research Institute, Boston, MA 02114, USA

10. Center for Molecular Medicine Cologne (CMMC), University of Cologne, 50937 Cologne, Germany

11. Cluster of Excellence Cellular Stress Responses in Aging-Associated Diseases (CECAD) Research Center, Joseph-Stelzmann-Str. 26, 50931 Cologne, Germany

Abstract

Corneal transparency and avascularity are essential for vision. The avascular cornea transitions into the vascularized conjunctiva at the limbus. Here, we explore a limbal stromal cell sub-population that expresses ABCB5 and has mesenchymal stem cell characteristics. Human primary corneal stromal cells were enriched for ABCB5 by using FACS sorting. ABCB5+ cells expressed the MSC markers CD90, CD73, and CD105. ABCB5+ but not ABCB5− cells from the same donor displayed evidence of pluripotency with a significantly higher colony-forming efficiency and the ability of trilineage differentiation (osteogenic, adipogenic, and chondrogenic). The ABCB5+ cell secretome demonstrated lower levels of the pro-inflammatory protein MIF (macrophage migration inhibitory factor) as well as of the pro-(lymph)angiogenic growth factors VEGFA and VEGFC, which correlated with reduced proliferation of Jurkat cells co-cultured with ABCB5+ cells and decreased proliferation of blood and lymphatic endothelial cells cultured in ABCB5+ cell-conditioned media. These data support the hypothesis that ABCB5+ limbal stromal cells are a putative MSC population with potential anti-inflammatory and anti-(lymph)angiogenic effects. The therapeutic modulation of ABCB5+ limbal stromal cells may prevent cornea neovascularization and inflammation and, if transplanted to other sites in the body, provide similar protective properties to other tissues.

Publisher

MDPI AG

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