TY - JOUR
T1 - Evaluating the effects of immunosuppression by in-vivo bioluminescence imaging after allotransplantation of ovarian grafts
AU - Lin, Yi Hsin
AU - Yeh, Yu Chi
AU - Tzeng, Chii Ruey
AU - Shang, Wei Jen
AU - Liu, Jah Yao
AU - Chen, Chi Huang
PY - 2011/2
Y1 - 2011/2
N2 - Bioluminescence imaging (BLI) has been introduced for studies of ongoing biological processes but has never been applied for ovarian transplantation. Here, BLI was used as a novel approach to trace the survival of ovarian grafts. The ovarian donors were transgenic mice carrying FVB/N-Tg (PolII-luc) as a reporter gene, encoding luciferase to catalyse luciferin which results in visible light emission as bioluminescence. There were three groups of recipients: (i) group A: BALB/c mice without immunosuppressant treatment; (ii) group B: BALB/c mice receiving a cocktail immunosuppressant treatment; and (iii) group C: immunodeficient NOD-SCID mice without immunosuppression. Luciferin BLI was used to follow graft survival, and viable follicle numbers were counted as a measure of success. Bioluminesence intensity fluctuated but was consistent with the end-point counts of viable follicle numbers. Group A showed loss of viable follicles and bioluminesence disappeared as early as day 10 following ovarian engraftment, indicating strong immune rejection. Groups B and C showed graft survival and measurable bioluminesence for up to 30 days. In conclusion, BLI provided non-invasive longitudinal dynamic monitoring of ovarian grafts with excellent sensitivity and spatial resolution. This approach should prove valuable for research on ovarian transplantation. Bioluminescence imaging (BLI) has been introduced for studies of ongoing biological processes but has never been applied for ovarian transplantation. Here, we used BLI as a novel approach to trace the survival of ovarian grafts. The ovarian donors were transgenic mice carrying FVB/N-Tg (PolII-luc) as a reporter gene encoding luciferase to catalyse luciferin, resulting in visible light emission as bioluminescence. There were three groups of recipients: group A, BALB/c mice without immunosuppressant treatment; group B, BALB/c mice receiving a cocktail immunosuppressant treatment and group C, immunodeficient NOD-SCID mice without immunosuppression. Luciferin BLI was used to follow engrafted tissue survival, and viable follicle numbers were counted as a measure of success. We found that bioluminescence intensity fluctuated but was consistent with the end-point counts of viable follicle numbers. Group A showed loss of viable follicles, and bioluminescence disappeared as early as the 10th day following ovarian engraftment, indicating strong immune rejection. Groups B and C showed graft survival and measurable BLI for up to 30 days. In conclusion, BLI provided non-invasive longitudinal dynamic monitoring of ovarian grafts with excellent sensitivity and spatial resolution. This approach should prove valuable for research on ovarian transplantation.
AB - Bioluminescence imaging (BLI) has been introduced for studies of ongoing biological processes but has never been applied for ovarian transplantation. Here, BLI was used as a novel approach to trace the survival of ovarian grafts. The ovarian donors were transgenic mice carrying FVB/N-Tg (PolII-luc) as a reporter gene, encoding luciferase to catalyse luciferin which results in visible light emission as bioluminescence. There were three groups of recipients: (i) group A: BALB/c mice without immunosuppressant treatment; (ii) group B: BALB/c mice receiving a cocktail immunosuppressant treatment; and (iii) group C: immunodeficient NOD-SCID mice without immunosuppression. Luciferin BLI was used to follow graft survival, and viable follicle numbers were counted as a measure of success. Bioluminesence intensity fluctuated but was consistent with the end-point counts of viable follicle numbers. Group A showed loss of viable follicles and bioluminesence disappeared as early as day 10 following ovarian engraftment, indicating strong immune rejection. Groups B and C showed graft survival and measurable bioluminesence for up to 30 days. In conclusion, BLI provided non-invasive longitudinal dynamic monitoring of ovarian grafts with excellent sensitivity and spatial resolution. This approach should prove valuable for research on ovarian transplantation. Bioluminescence imaging (BLI) has been introduced for studies of ongoing biological processes but has never been applied for ovarian transplantation. Here, we used BLI as a novel approach to trace the survival of ovarian grafts. The ovarian donors were transgenic mice carrying FVB/N-Tg (PolII-luc) as a reporter gene encoding luciferase to catalyse luciferin, resulting in visible light emission as bioluminescence. There were three groups of recipients: group A, BALB/c mice without immunosuppressant treatment; group B, BALB/c mice receiving a cocktail immunosuppressant treatment and group C, immunodeficient NOD-SCID mice without immunosuppression. Luciferin BLI was used to follow engrafted tissue survival, and viable follicle numbers were counted as a measure of success. We found that bioluminescence intensity fluctuated but was consistent with the end-point counts of viable follicle numbers. Group A showed loss of viable follicles, and bioluminescence disappeared as early as the 10th day following ovarian engraftment, indicating strong immune rejection. Groups B and C showed graft survival and measurable BLI for up to 30 days. In conclusion, BLI provided non-invasive longitudinal dynamic monitoring of ovarian grafts with excellent sensitivity and spatial resolution. This approach should prove valuable for research on ovarian transplantation.
KW - bioluminescence imaging
KW - ovarian transplantation
UR - http://www.scopus.com/inward/record.url?scp=79551566272&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79551566272&partnerID=8YFLogxK
U2 - 10.1016/j.rbmo.2010.10.010
DO - 10.1016/j.rbmo.2010.10.010
M3 - Article
C2 - 21233017
AN - SCOPUS:79551566272
SN - 1472-6483
VL - 22
SP - 220
EP - 227
JO - Reproductive BioMedicine Online
JF - Reproductive BioMedicine Online
IS - 2
ER -