A NEW METHOD FOR VITAL STAINING OF CENTRAL NERVOUS TISSUES WITH NEUTRAL RED

1971 ◽  
Vol 21 (1) ◽  
pp. 151-155
Author(s):  
Ryuei Maeda ◽  
Nobuo Ihara ◽  
Reiko Takada ◽  
Tadashi Kondo ◽  
Emyo Nakano ◽  
...  
Development ◽  
1986 ◽  
Vol 94 (1) ◽  
pp. 231-244
Author(s):  
J. M. Hurle ◽  
Y. Gañan

In the present work, we have analysed the possible involvement of ectodermal tissue in the control of interdigital mesenchymal cell death. Two types of experiments were performed in the stages previous to the onset of interdigital cell death: (i) removal of the AER of the interdigit; (ii) removal of the dorsal ectoderm of the interdigit. After the operation embryos were sacrificed at 10–12h intervals and the leg buds were studied by whole-mount cartilage staining, vital staining with neutral red and scanning electron microscopy. Between stages 27 and 30, ridge removal caused a local inhibition of the growth of the interdigit. In a high percentage of the cases, ridge removal at these stages was followed 30–40 h later by the formation of ectopic nodules of cartilage in the interdigit. The incidence of ectopic cartilage formation was maximum at stage 29 (60%). In all cases, cell death took place on schedule although the intensity and extent of necrosis appeared diminished in relation to the intensity of inhibition of interdigital growth and to the presence of interdigital cartilages. Ridge removal at stage 31 did not cause inhibition of the growth of the interdigit and ectopic chondrogenesis was only detected in 3 out of 35 operated embryos. Dorsal ectoderm removal from the proximal zone of the interdigit at stage 29 caused the chondrogenesis of the proximal interdigital mesenchyme in 6 out of 18 operated embryos. The pattern of neutral red vital staining was consistent with these results revealing a partial inhibition of interdigital cell death in the proximal zone of the interdigit. It is proposed that under the present experimental conditions the mesenchymal cells are diverted from the death programme by a primary transformation into cartilage.


1957 ◽  
Vol 65 (2-3) ◽  
pp. 139-144 ◽  
Author(s):  
Mizu Kojima ◽  
Tutomu Watanuki
Keyword(s):  

2009 ◽  
Vol 56 (5) ◽  
pp. 742-750 ◽  
Author(s):  
KIRSTEN MARNER ◽  
MOGENS S. NORN
Keyword(s):  

1927 ◽  
Vol 2 (1) ◽  
pp. 17-18 ◽  
Author(s):  
Max Phillips ◽  
Barnett Cohen
Keyword(s):  

2021 ◽  
Vol 9 (6) ◽  
pp. 616
Author(s):  
Dor Shefy ◽  
Nadav Shashar ◽  
Baruch Rinkevich

Xenogeneic and allogeneic encounters following aggregated and clustered settlements of coral larvae (planulae) may carry important ecological consequences in shaping coral reefs’ communities. However, larval settlement behaviors and settlement location choices in the presence of conspecifics or heterospecifics have not been examined in detail, due to a lack of experimental tools. One potential approach is the employment of vital staining of planulae with dyes that do not impair larval metamorphosis processes, are stable for prolonged periods, and do not diffuse to un-labeled counterpart planulae. For these purposes, we examined the use of neutral red (NR) dye, as an identification marker, on the planulae of Stylophora pistillata, a Red Sea branching coral species. To examine possible NR impacts on larval settlement in the presence of conspecific planulae, we followed the settlement ratios of kin, non-kin, and mixed assemblages, as a proxy for metamorphosis success. We found no differences in settlement rates of stained vs. unstained larvae, lack of stain diffusion to other larvae and that NR stain is maintained for more than a week under a still water regimen. Thus, staining with NR may serve as a useful experimental tool, opening new opportunities in studying larval settlement patterns in sessile marine organisms.


2017 ◽  
Author(s):  
Koji Makanae

It has been reported that the intracellular pH of the budding yeast Saccharomyces cerevisiae is asymmetric between mother and daughter cells, and this asymmetry in pH underlies replicative aging and rejuvenation. S. cerevisiae growth morphology changes between the yeast form and pseudohyphal form, according to nutrient availability. A previous study reported that the replicative life span of pseudohyphal form cells is longer than that of yeast form cells in S. cerevisiae. However, the intracellular pH of pseudohyphal cells is unknown. To examine the intracellular pH of S. cerevisiae cells during pseudohyphal growth, vital staining was performed with neutral red, which is a pH indicator, of cells growing on nitrogen starvation (SLAD) medium. The results showed that the vacuoles of S. cerevisiae cells during pseudohyphal growth induced by nitrogen starvation formed polar pH gradients. The relationship between cell size and shape and the neutral red staining patterns suggested that the pH of cell vacuoles during pseudohyphal growth changed from uniformly near pH 6.8 to steep gradients of pH from vacuole ends along the long axis of the cell. The results of time-lapse imaging to examine vacuolar dynamics and neutral red staining suggested that the pH gradients were not formed simply by inheritance of vacuolar contents accompanying vacuolar movements.


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