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Xabier L. Aranguren, Jonathan D. McCue, Benoit Hendrickx, Xiao-Hong Zhu, Fei Du, Eleanor Chen, Beatriz Pelacho, Ivan Peñuelas, Gloria Abizanda, Maialen Uriz, Sarah A. Frommer, Jeffrey J. Ross, Betsy A. Schroeder, Meredith S. Seaborn, Joshua R. Adney, Julianna Hagenbrock, Nathan H. Harris, Yi Zhang, Xiaoliang Zhang, Molly H. Nelson-Holte, Yuehua Jiang, An D. Billiau, Wei Chen, Felipe Prósper, Catherine M. Verfaillie, Aernout Luttun
Published in Volume 118, Issue 2
J Clin Invest. 2008; 118(2):505–514 doi:10.1172/JCI31153
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Figure 6
Effects of mMAPC-U and hMAPC-U in severe ischemia.

(AD) α-SMA (red) staining at 21 days in adductor of vehicle- (A), mMAPC-U– (B), mMAPC-U2– (C), or hMAPC-U–treated mice (D). Overexposure in the DAPI channel was used to reveal muscle tissue. (E and F) Laser Doppler measurements (E) in left legs (expressed as % improvement versus pretransplant [day +5] and relative to the nonligated right leg); and treadmill endurance test (F) measuring hind limb function (expressed as % of pretransplant performance [day +5]) at several time points after (+) ligation of vehicle- (red), mMAPC-U– (black), mMAPC-U2– (gray), or hMAPC-U–treated mice (blue). (GJ) Sirius red–stained cross sections of gastrocnemius muscle 3 weeks after transplantation of vehicle- (G), mMAPC-U– (H), mMAPC-U2– (I), or hMAPC-U–injected (J) animals. (K) Quantitative analysis of α-SMA (in adductor), viability (TTC), fibrosis (Sirius red), and myogenesis (desmin) staining (all in gastrocnemius), expressed as percent positive staining per muscle area in vehicle- (red), mMAPC-U– (black), mMAPC-U2– (gray), or hMAPC-U–treated mice (blue). All analyses were performed on 6–12 mice per group. *P < 0.05 versus vehicle for each corresponding time point; P = 0.05 versus vehicle; #P = 0.07 versus vehicle. Scale bars: 250 μm (AD) and 62.5 μm (GJ).