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. 2011 Apr 26;301(1):E91–E98. doi: 10.1152/ajpendo.00701.2010

Fig. 1.

Fig. 1.

Premature aging phenotypes in testicular nuclear receptor 4 (TR4)−/− mice. A: 1-yr survival rate between TR4+/+, TR4+/−, and TR4−/− mice (n = 74 for TR4+/+ and TR4+/− mice, n = 77 for TR4−/− mice). B: general appearance of TR4−/− [knockout (KO)] mice. Gray hair and hunchback were seen in 6-mo-old TR4−/− female mice compared with age-matched TR4+/+ [wild-type (WT)] mice. C: extramedullary hematopoiesis in 6-mo-old TR4−/− mice liver. D: radiograph of 3- and 6-mo-old TR4−/− and TR4+/+ mice showed skeletal abnormalities in aging TR4−/− mice. Six-month-old TR4−/− mice display curvature of the spinal column (kyphosis). Pictures from BD are the representative pictures from ≥3 pairs of WT and KO mice. E: dual-energy X-ray absorptiometry scan analyses of young (2–4 mo; n = 4) and old male TR4−/− mice (n = 5) at the age of 6–7 mo compared with age/sex-matched TR4+/+ mice. Differences in bone mineral density (BMD) of a particular sex and genotypes were analyzed by Student's t-test *P < 0.05.