دورية أكاديمية

Different Innate Immune Responses in BALB/c and C57BL/6 Strains following Corneal Transplantation.

التفاصيل البيبلوغرافية
العنوان: Different Innate Immune Responses in BALB/c and C57BL/6 Strains following Corneal Transplantation.
المؤلفون: Bleul T; Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany., Zhuang X; Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany., Hildebrand A; Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany., Lange C; Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany., Böhringer D; Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany., Schlunck G; Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany., Reinhard T; Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany., Lapp T; Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany, thabo.lapp@uniklinik-freiburg.de.
المصدر: Journal of innate immunity [J Innate Immun] 2021; Vol. 13 (1), pp. 49-59. Date of Electronic Publication: 2020 Sep 09.
نوع المنشور: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 101469471 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1662-8128 (Electronic) Linking ISSN: 1662811X NLM ISO Abbreviation: J Innate Immun Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : Karger, c2009-
مواضيع طبية MeSH: Corneal Transplantation*, Anterior Eye Segment/*immunology , Graft Rejection/*immunology , Macrophages/*immunology, ADP-ribosyl Cyclase 1/metabolism ; Animals ; Anterior Eye Segment/diagnostic imaging ; Antigens, Differentiation/metabolism ; Cell Movement ; Genetic Background ; Genetic Predisposition to Disease ; Graft Rejection/genetics ; Immunity, Innate/genetics ; Macrophage Activation ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Tomography, Optical Coherence ; Transplantation, Homologous ; Transplantation, Isogeneic
مستخلص: Purpose: To investigate immunological differences and the role of CD38+/F4/80 + M1 macrophages in C57BL/6J- and BALB/c-recipient mouse corneal transplantation models.
Methods: Allogeneic transplantation was performed crosswise in BALB/c mice and C57BL/6J mice; syngeneic transplantation was performed in both strains. Anterior chamber depth (ACD) was measured before and central corneal thickness (CCT) was measured both before and after transplantation. In vivo graft rejection was monitored using anterior eye segment optical coherence tomography (ASOCT) evaluating the CCT and grading of corneal oedema using a well-established clinical score (CS). Histology of corneal grafts was performed 18 or 21 days after surgery. Immunohistochemistry with anti-F4/80 antibody and anti-CD38 antibody was used for detecting M1 macrophages within the grafts.
Results: High CS and CCT values after allogeneic transplantation persisted in both BALB/c (n = 18) and C57BL/6J recipients (n = 20). After syngeneic transplantation, CS and CCT values increased in both models in the early phase after surgery due to the surgical trauma. Surprisingly, in the syngeneic C57BL/6J model, high CCT values persisted. Furthermore, anterior synechiae developed in C57BL/6 recipients after both syngeneic and allogeneic transplantation, whereas BALB/c recipients showed almost no synechiae - even though C57/BL6J animals tended to have a deeper anterior chamber (281 ± 11 pixels [mean ± SD]) compared with BALB/c animals of the same age (270 ± 9 pixels [mean ± SD]). Immunohistochemistry revealed numerous CD38+/F4/80 + M1 macrophages in grafts of C57BL/6J recipients following both syngeneic and allogeneic transplantation. However, in BALB/c-recipient mice only sparse M1 macrophages were detectable (CD38 + M1 macrophages relative to all F4/80 + cells: 75 vs. 17% [after allogeneic transplantation] and 66 vs. 17% [after syngeneic transplantation]; p < 0.05).
Conclusions: Allogeneic corneal transplants are rejected in BALB/c as well as C57BL/6J mice, but tissue alterations with anterior synechiae are more pronounced in C57BL/6J recipients. Following syngeneic transplantation, C57BL/6J-recipient animals show a persistent graft swelling with increased numbers of CD38+/F4/80 + M1 macrophages in grafted tissue, in contrast to the common model using BALB/c-recipient mice. Our data strongly suggest that strain-dependent differences convey different innate immune responses in BALB/c and C57BL/6J strains. Accordingly, in murine keratoplasty experiments, the mouse line of both donor and recipient animals must be carefully considered. C57BL/6J-recipient mice might be particularly suited to study corneal graft rejection in a clinical setting considered "high risk."
(© 2020 The Author(s) Published by S. Karger AG, Basel.)
References: J Am Acad Dermatol. 2006 Jan;54(1):1-15; quiz 16-8. (PMID: 16384751)
Arch Ophthalmol. 1991 Feb;109(2):244-51. (PMID: 1993036)
Oncoimmunology. 2017 Dec 26;7(4):e1409929. (PMID: 29632723)
Invest Ophthalmol Vis Sci. 1997 Dec;38(13):2833-43. (PMID: 9418737)
Front Immunol. 2018 Jul 10;9:1593. (PMID: 30042766)
Transplantation. 2005 Jan 15;79(1):23-31. (PMID: 15714165)
Immunology. 2010 Apr;129(4):556-66. (PMID: 20102413)
Invest Ophthalmol Vis Sci. 2000 Oct;41(11):3341-7. (PMID: 11006223)
Mol Vis. 2016 Oct 17;22:1248-1255. (PMID: 27777504)
Cornea. 2018 Jan;37(1):95-101. (PMID: 29023237)
Hum Gene Ther. 2018 Apr;29(4):467-479. (PMID: 28990426)
Transpl Immunol. 1996 Mar;4(1):53-6. (PMID: 8762011)
Invest Ophthalmol Vis Sci. 1995 Jul;36(8):1530-40. (PMID: 7601633)
J Exp Med. 2002 Jan 21;195(2):259-68. (PMID: 11805152)
Mol Vis. 2007 Apr 27;13:626-34. (PMID: 17515886)
Invest Ophthalmol Vis Sci. 2018 Aug 1;59(10):3911-3919. (PMID: 30073362)
Exp Eye Res. 2018 Apr;169:141-148. (PMID: 29305888)
Eur J Immunol. 2011 Sep;41(9):2472-6. (PMID: 21952799)
Transplantation. 2008 Dec 27;86(12):1720-4. (PMID: 19104411)
JAMA Ophthalmol. 2016 Feb;134(2):167-73. (PMID: 26633035)
Cornea. 2009 Sep;28(8):865-70. (PMID: 19654531)
PLoS One. 2018 Apr 4;13(4):e0194855. (PMID: 29617399)
Invest Ophthalmol Vis Sci. 2000 Jul;41(8):2239-47. (PMID: 10892868)
PLoS One. 2015 Dec 23;10(12):e0145342. (PMID: 26699615)
Immunology. 2016 May;148(1):102-13. (PMID: 26840507)
Exp Parasitol. 1988 Apr;65(2):258-68. (PMID: 3127233)
Nat Rev Immunol. 2008 Dec;8(12):958-69. (PMID: 19029990)
Invest Ophthalmol Vis Sci. 2019 Aug 1;60(10):3669-3679. (PMID: 31469894)
Trends Immunol. 2003 Nov;24(11):570-4. (PMID: 14596877)
Invest Ophthalmol Vis Sci. 2015 Nov;56(12):7250-9. (PMID: 26544793)
Am J Trop Med Hyg. 1982 Mar;31(2):230-8. (PMID: 6462064)
Ophthalmic Surg. 1990 Nov;21(11):781-5. (PMID: 2270163)
Invest Ophthalmol Vis Sci. 2002 Jul;43(7):2264-71. (PMID: 12091426)
Biomed Pharmacother. 2019 May;113:108558. (PMID: 30856534)
BMC Microbiol. 2018 May 30;18(1):45. (PMID: 29848308)
Sci Rep. 2017 Apr 20;7(1):971. (PMID: 28428556)
Immunity. 2014 Jul 17;41(1):14-20. (PMID: 25035950)
Cornea. 2019 Jun;38(6):742-747. (PMID: 30882541)
Invest Ophthalmol Vis Sci. 2018 Oct 1;59(12):5277-5284. (PMID: 30383199)
J Immunol. 2000 Jun 15;164(12):6166-73. (PMID: 10843666)
Invest Ophthalmol Vis Sci. 2019 Nov 1;60(14):4511-4519. (PMID: 31675422)
Am J Transplant. 2013 Jun;13(6):1461-73. (PMID: 23679575)
Biochem Biophys Res Commun. 2018 Jan 15;495(3):2338-2343. (PMID: 29274779)
BMC Ophthalmol. 2015 Jul 29;15:87. (PMID: 26219961)
Graefes Arch Clin Exp Ophthalmol. 1985;222(3):128-33. (PMID: 3884454)
Front Immunol. 2018 Oct 01;9:2246. (PMID: 30327653)
Arch Ophthalmol. 2006 Jan;124(1):62-9. (PMID: 16401786)
فهرسة مساهمة: Keywords: BALB/c; C57BL/6; Corneal graft rejection; Keratoplasty; Macrophage
المشرفين على المادة: 0 (Antigens, Differentiation)
0 (monocyte-macrophage differentiation antigen)
EC 3.2.2.6 (ADP-ribosyl Cyclase 1)
تواريخ الأحداث: Date Created: 20200909 Date Completed: 20211111 Latest Revision: 20211111
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC7879253
DOI: 10.1159/000509716
PMID: 32906119
قاعدة البيانات: MEDLINE
الوصف
تدمد:1662-8128
DOI:10.1159/000509716