Osawa Hideya, Maruyama Kazuichi, Streilein J Wayne
Schepens Eye Research Institute, Harvard Department of Ophthalmology, Boston, Massachusetts 02114, USA.
Invest Ophthalmol Vis Sci. 2004 Jun;45(6):1908-15. doi: 10.1167/iovs.03-0512.
To determine the extent to which CD95 ligand (CD95L) expressed on corneal epithelium and endothelium influences survival of cornea grafts placed orthotopically and heterotopically in the anterior chamber (AC), an immune-privileged site.
Corneas from eyes of C57BL/6 (B6) and B6.gld (CD95L deficient) mice were (1) rendered into small full-thickness fragments, with or without an epithelial layer, and placed behind recipient corneas in the ACs of BALB/c eyes, while BALB/c corneas were similarly implanted in eyes of B6 and B6.lpr (CD95 deficient) mice; or (2) corneas were grafted orthotopically in BALB/c eyes as intact corneas or as composite corneas in which epithelium from one donor source was layered in vitro onto epithelium-deprived stroma+endothelium from another donor source before grafting. The fate of the grafts was assessed clinically and histologically, and the capacity of the grafts to sensitize recipient mice to donor alloantigens (delayed hypersensitivity, DH) was evaluated.
Allogeneic, full-thickness B6.gld corneal fragment grafts placed in the AC of BALB/c mice were rejected and sensitized their recipients, whereas epithelium-deprived B6.gld cornea fragments survived indefinitely and failed to sensitize their recipients. BALB/c corneal fragment grafts placed in the AC of C57BL/6 or B6.lpr eyes were rejected. Orthotopic cornea grafts composed of B6.gld epithelium layered onto wild-type B6 stroma and endothelium were rejected at a tempo and incidence similar to full-thickness B6 grafts, whereas orthotopic composite cornea grafts containing B6 epithelium layered onto B6.gld stroma+endothelium were vigorously rejected.
CD95L expression on epithelium of full-thickness cornea fragment grafts placed in the anterior chamber of BALB/c eyes protects these heterotopic grafts from rejection but has only a trivial role to play in determining the fate of orthotopic corneal grafts. In the latter type of corneal grafts, CD95L expression on the endothelium plays an essential role in preventing graft rejection.
确定角膜上皮和内皮表达的CD95配体(CD95L)在多大程度上影响原位和异位植入前房(一个免疫赦免部位)的角膜移植片的存活。
将C57BL/6(B6)和B6.gld(CD95L缺陷型)小鼠眼中的角膜(1)制成有或无上皮层的小全层碎片,置于BALB/c小鼠前房的受体角膜后方,同时将BALB/c角膜类似地植入B6和B6.lpr(CD95缺陷型)小鼠眼中;或者(2)将角膜作为完整角膜原位移植到BALB/c小鼠眼中,或者作为复合角膜移植,即将来自一个供体来源的上皮在体外分层到来自另一个供体来源的无上皮基质+内皮上,然后进行移植。临床和组织学评估移植片的转归,并评估移植片使受体小鼠对供体同种异体抗原致敏的能力(迟发型超敏反应,DH)。
置于BALB/c小鼠前房的同种异体全层B6.gld角膜碎片移植片被排斥并使受体致敏,而无上皮的B6.gld角膜碎片可无限期存活且未使受体致敏。置于C57BL/6或B6.lpr小鼠前房的BALB/c角膜碎片移植片被排斥。由B6.gld上皮分层到野生型B6基质和内皮上组成的原位角膜移植片的排斥速度和发生率与全层B6移植片相似,而含有B6上皮分层到B6.gld基质+内皮上的原位复合角膜移植片被强烈排斥。
置于BALB/c小鼠前房的全层角膜碎片移植片上皮上的CD95L表达可保护这些异位移植片不被排斥,但在决定原位角膜移植片的转归中仅起微不足道的作用。在后一种类型的角膜移植片中,内皮上的CD95L表达在防止移植片排斥中起重要作用。