FIGURE

Figure 3

ID

ZDB-FIG-200314-12

Publication

Cirrincione et al., 2020 - Paclitaxel-induced peripheral neuropathy is caused by epidermal ROS and mitochondrial damage through conserved MMP-13 activation

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Figure 3

Axonal mitochondria are vacuolized following paclitaxel treatment but ROS/H₂O₂ levels are not elevated. (a,b) DsRed-labeled mitochondria in unmyelinated axons of somatosensory neurons labeled with CREST3:GFP following 4 hr treatment with vehicle (a) or paclitaxel (b). (c,d) Respective 3D reconstructions of axon branch segment (blue) in the epidermis containing mitochondria (pink, arrows). (e–i) Quantification of axonal mitochondria shows increased diameter (e), length (f), length-width ratio (g) and number of mitochondria per branch segment (h,i), n = 5 animals per treatment group. (j) TEM analysis of axonal mitochondria (M) following treatment with 0.09% DMSO vehicle, paclitaxel with or without MMP-13 inhibitor (Cl-82198 top and DB04760 bottom) for 3 hr and 96 hr shows rapid paclitaxel-induced mitochondria vacuolization (red arrows) and membrane disruptions (yellow arrows), persisting up to 96 hr, similar to paclitaxel + MMP-13 inhibitor. (k) Axonal HyPer oxidation is elevated after DMSO treatment for 3 hr but not after prolonged treatment with either DMSO or paclitaxel, n = 5–7 animals per treatment group. Abbreviations: B = basal keratinocyte, P = periderm, M = mitochondrion, Ax = axon, Ac = Actinotrichia.

Expression Data

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Antibody Labeling

Phenotype Data

Phenotype Detail

Acknowledgments

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