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Biomedical subjects

I Iuchi

Publications and source records attributed to I Iuchi.

At least 73 records · Page 4Linked to original sources
PubMed1975

Electron microscopic study of erythrocytes in developing rainbow trouts, Salmo gairdnerii irideus, with particular reference to changes in the cell line.

The fine structure of the first erythroid cells in the embryonic circulation of the rainbow trout and new erythroid cells appearing after hatching was examined by scanning and transmission electron microscopy. The first erythroid cells in the embryos, where circulation has just begun, are very immature in ultrastructural characteristics; they are spherical, relatively large, and contain a large nucleus with diffuse chromatin and numerous free ribosomes mostly occurring as polyribosomes. The cells divide in the circulatory system. As development proceeds, the entire population undergoes a synchronous maturation, i.e., transformation into round and flat discs, progressive heterochromatization, reduction in number of cytoplasmic organelles, especially of ribosomes, and a concomitant increase of hemoglobin content. The fully mature first erythroid cells persist until after hatching and are gradually replaced by a new population of erythroid cells which begin to appear in the circulatory system within a few days after hatching. The new cells are at first small and spherical, and show immature ultrastructural features, but no dividing cells were encountered. The cytological changes accompanying maturation are almost parallel to those seen in the first class of erythroid cells. In the circulatory system of fry, where yolk absorption has just been completed, almost all the erythroid cells are mature. These cells are uniformly flat and elliptical discs. The differences in ribosome numbers in electron micrographs of erythroid cells from different stages of development are also consistent with the existence of two series of erythroid cell maturation in the peripheral blood of the developing rainbow trout.

Animals↗
PubMed1975

Ontogenetic expression of larval and adult hemoglobin phenotypes in the intergeneric salmonid hybrids.

Ontogeny of the hemoglobins of Honmasu (Oncorhynchus rhodurus, HXH),brook trout (Salvelinus fontinalis, BXB) and their reciprocal hybrids (HXB and BXH) was examined electrophoretically as well as spectrophotometrically. All of these fish have electrophoretically distinct larval and adult type hemoglobins and the transition from one type to the other occurred early during post-hatching development. In the case of larval hemoglobins, the electrophoretic pattern of a hybrid, BXH, resembled that of the maternal parent, brook trout (BXB), while the hemoglobin of the reciprocal hybrid, HXB, differed markedly from that of the maternal parent, Honmasu (HXH), in that it possesses a diffuse pattern. Spectrophotometric examinations indicated that this was mostly methemoglobin. Adult type hemoglobins at more advanced stages of both hybrids were electrophoretically resolved into the parental hemoglobins. However, no "hybrid" hemoglobins were detected. Because there was abnormal hemoglobin formation in the larval erythrocytes (erythrocytes L) of the HXB hybrid, and then normal hemoglobin synthesis in the adult erythrocytes (erythrocytes A) of the same fish at later developmental stages, it appears that the paternal effects upon the hemoglobin differed in these two erythroid cell lines of the developing trout.

Animals↗
PubMed1969

Hemoglobin Hiroshima (beta-143 histidine--aspartic acid): a newly identified fast moving beta chain variant associated with increased oxygen affinity and compensatory erythremia.

During a survey for hemoglobinopathies in over 9000 residents of Hiroshima Prefecture, Japan, a fast moving hemoglobin was identified in eight members of three generations in a Japanese family. The abnormal hemoglobin, named Hb Hiroshima, constitutes about 50% of the total hemoglobin in hemolysates from the carriers who have a mild erythremia but are otherwise apparently clinically unaffected. All preparations of Hb Hiroshima have increased affinity for oxygen, by either tonometric or oxygen electrode determinations. At pH 7.0, the oxygen pressure, P(50) required to half saturate an unfractionated hemolysate from a carrier was one-half that of Hb A, and the P(50) of a purified sample containing no Hb A was one-fourth that of Hb A. The pH dependence of the oxygen equilibrium (Bohr effect) is below normal, as shown by the absolute value of the Bohr effect factor which is about half that of Hb A, in the pH range between 7.0 and 7.4. The Hill constant, n, for Hb Hiroshima between pH 7.0 and 7.4 is 2-2.4, compared to 2.8-3 for Hb A under the same conditions, indicating reduction of, but not complete abolition of heme-heme interaction. Urea dissociation and canine hybridization tests located the biochemical lesion in the beta chain. Fingerprints (Ingram), carboxypeptidase digestion, and amino acid analysis demonstrated that the substitution was at residue 143 in the beta chain, where histidine was replaced by aspartic acid.In contrast to other recently described high oxygen affinity mutants that show intact Bohr effects, all three of the major characteristics of the reversible combination of hemoglobin with oxygen (oxygen equilibrium, heme-heme interaction, and pH dependence) are affected in Hb Hiroshima. A tentative interpretation of these effects, relating structure to function, is offered in terms of recently developed models of normal hemoglobin.

Blood Protein Electrophoresis↗
PubMed1968

Hemoglobin Hijiyama: a new fast-moving hemoglobin in a Japanese family.

A variant of hemoglobin A, named Hb Hijiyama, found in two generations of a Japanese family living in Hiroshima, Japan, has a higher anodal electrophoretic mobility than hemoglobin A; a gain of two negative charges per molecule is indicated. Fingerprinting and amino acid analysis showed the biochemical anomaly to be in the beta chain at residue 120, where lysine is replaced by glutamic acid. In the heterozygote carriers of the abnormal hemoglobin there is no apparent association with clinical or hematologic abnormalities.

Adult↗