FIGURE

Fig. S5

ID
ZDB-FIG-190812-40
Publication
Chen et al., 2019 - Cerebrovascular Injuries Induce Lymphatic Invasion into Brain Parenchyma to Guide Vascular Regeneration in Zebrafish
Other Figures
All Figure Page
Back to All Figure Page
Fig. S5

The regenerating blood vessels arise from residual blood vessels through cell proliferation and migration, Related to Figure 1. (A and B) At 1 dpt after Mtz treatment, the residual blood vessels CVP (A, arrow) and PHBC (B, arrow) were photoconverted from green to red fluorescence. At 5 dpt, retentions of the Dendra2-red fluorescence were detected in nascent blood vessels MMCtAs (A, arrowhead, n=9/10) and CtAs (B, arrowhead, n=8/10), respectively. (C and D) Live imaging of the nascent MMCtA and CtA formation. Nascent MMCtA was observed to migrate from CVP to BCA (C, arrowheads, n=10/10), while nascent CtA migrated from PHBC to BA (D, arrowheads, n=10/10), accompanied by explanatory schematic diagrams. (E–G) Illustration of hindbrain vascular network indicate the image area in following panels (E). In contrast to DMSO treatment in which brain BECs rarely proliferated (F, n=20/20), many of nascent BECs were positive for EdU labeling at 3 dpt after Mtz treatment (G, arrows, n=19/21). All images are dorsal view, anterior upward. Scale bar, 50 μm. BA, basilar artery; BCA, basal communicating artery; CtA, central artery; CVP, choroidal vascular plexus; MMCtA, middle mesencephalic central artery; PHBC, primordial hindbrain channel.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image.

Reprinted from Developmental Cell, 49(5), Chen, J., He, J., Ni, R., Yang, Q., Zhang, Y., Luo, L., Cerebrovascular Injuries Induce Lymphatic Invasion into Brain Parenchyma to Guide Vascular Regeneration in Zebrafish, 697-710.e5, Copyright (2019) with permission from Elsevier. Full text @ Dev. Cell