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Updated: Jul 27, 2025

Visualizing Scar Development Using SCAD Assay - An Ex-situ Skin Scarring Assay
Published on: April 28, 2022
SCN
Akiko Fujiwara1, Ikuo Yasumasu1
1Department of Biology, School of Education, Waseda University, 1-6-1 Nishiwaseda Shinjuku-ku, Tokyo 169, Japan.
Abstract:
Sea urchin eggs kept in artificial sea water (ASW) containing 0.01-0.3 M NaSCN in place of NaCI from within 2 min after insemination formed thin, enlarged fertilization envelopes, which were broken on mild agitation of egg suspensions more easily than those formed in Ca2+ -free ASW. The blastomeres of almost all embryos derived from eggs treated with 0.2M SCN- for 1 hr dissociated spontaneously, and did not reassociate with other blastomeres appreciably. Thus SCN- probably denaturated some compound(s) participating in blastomere binding and hardening of the fertilization envelope. Abnormal arrangements of blastomeres, probably due to incomplete blastomere dissociation, were observed in embryos derived from eggs treated with 0.1 M SCN- for 1 hr. Treatment of fertilized or unfertilized eggs with 0.05-0.1 M SCN- for a short period caused concentration-dependent block of morphogenic processes such as formation of the archenteron and pluteus arms in the post-hatching period. The effects of SCN- on morphogenesis were not inhibited by furosemide or 4,4'-diisothiocyano 2,2'-disulfonic stilbene. Presumably, the denaturation of several compounds in the egg surface by SCN- causes abnormal morphogenesis of embryos. The inhibitory effects of SCN- on hardening of the fertilization envelope, blastomere binding and morphogenesis were greater in the absence of Ca2+ .
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