| Literature DB >> 34774519 |
Zala Lužnik Marzidovšek1, Tomas Blanco2, Zhongmou Sun2, Hamid Alemi2, Gustavo Ortiz2, Hayate Nakagawa2, Sunil K Chauhan2, Andrew W Taylor3, Ula V Jurkunas2, Jia Yin4, Reza Dana5.
Abstract
Corneal transplantation is the most common form of tissue transplantation. The success of corneal transplantation mainly relies on the integrity of corneal endothelial cells (CEnCs), which maintain tissue transparency by pumping out excess water from the cornea. After transplantation, the rate of CEnC loss far exceeds that seen with normal aging, which can threaten sight. The underlying mechanisms are poorly understood. Alpha-melanocyte-stimulating hormone (α-MSH) is a neuropeptide that is constitutively found in the aqueous humor with both cytoprotective and immunomodulatory effects. The curent study found high expression of melanocortin 1 receptor (MC1R), the receptor for α-MSH, on CEnCs. The effect of α-MSH/MC1R signaling on endothelial function and allograft survival in vitro and in vivo was investigated using MC1R signaling-deficient mice (Mc1re/e mice with a nonfunctional MC1R). Herein, the results indicate that in addition to its well-known immunomodulatory effect, α-MSH has cytoprotective effects on CEnCs after corneal transplantation, and the loss of MC1R signaling significantly decreases long-term graft survival in vivo. In conclusion, α-MSH/MC1R signaling is critical for CEnC function and graft survival after corneal transplantation.Entities:
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Year: 2021 PMID: 34774519 PMCID: PMC8908049 DOI: 10.1016/j.ajpath.2021.10.016
Source DB: PubMed Journal: Am J Pathol ISSN: 0002-9440 Impact factor: 4.307