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I Takeuchi

Publications and source records attributed to I Takeuchi.

At least 55 records · Page 3Linked to original sources
PubMed1998

[Clinical study of long graft survival in renal transplantation recipients].

BACKGROUND: A total of 110 patients, in whom kidneys from 95 living related and 15 cadaver donor, had experienced renal transplantation between February 1985 and October 1996 in our clinic. This study was conducted to evaluate the influence of the various pre-operative factors to the graft survivals and clinical course of patients in living related renal transplantation. METHODS: In 95 recipients, 17 adult patients had long term graft survivals over 5 years including 6 recurrent or denovo nephritis without chronic allografts nephropathy. Eight failed to graft loss attributed to chronic allografts nephropathy diagnosed within 5 years. Retrospective analysis were performed to elucidate the differences of these recipients. RESULTS: Donors of long graft survival recipients were younger (49.1 +/- 12.1 v.s. 58.9 +/- 10. 2) and had a better renal function evaluated by preoperative creatinine clearance in living related donors (115.5 +/- 37.0 v.s. 79.7 +/- 22.0 1/day). Graft long survival recipients had experienced less frequencies of acute rejection within 6 months (0.53 +/- 0.62: 8 patients, 9 times) compared with chronic allografts nephropathy recipients (1.00 +/- 0.53: 7 patients, 8 times). Long graft survival recipients had better responses to the antirejection therapy. Additionally acute rejection over 6 months were experienced only in chronic allografts nephropathy recipients. Higher serum creatinine level was revealed in recipients with chronic allografts nephropathy at 1 year after transplantation (1.27 +/- 0.27 v.s. 1.88 +/- 0.42 mg/dl). CONCLUSIONS: We concluded that donor age and renal function are related to the graft long survival as background factors. Long graft survival recipients had less frequency of acute rejection and good response to the antirejection therapy. In recipients with of acute rejection and good response to the antirejection therapy. In recipients with chronic allografts nephropathy, serum cretine level had already increased gradually within 1 year.

Adult↗
PubMed1997

Kidney-alone transplantation in diabetic patients with end-stage renal disease.

From January 1989 to December 1995, 5 diabetic patients with end-stage renal disease (1 woman, 4 men) underwent kidney-alone transplantation. The mean age of the recipients at the time of transplantation was 37.4 years (range, 32 to 43). Craft function and glucose tolerance was evaluated for 5 to 72 months after surgery. Postoperative complications were seen in 2 patients; nonspecific subcutaneous infections and an asymptomatic partial allograft infarction. All renal allografts were functioning 1 year after transplantation, with a mean serum creatinine level of 1.10 mg/dL (range, 0.8 to 1.8 mg/dL), and a mean urinary protein level of 17.8 mg/dL (range, 5 to 27 mg/dL). The postoperative daily dose of insulin was higher than the preoperative dose, while the level of glycated hemoglobin (HbA1C) increased after surgery and peaked 6 months after transplantation; 1 year after transplantation it had reverted to the preoperative level. As long as the diabetic complications of the renal allograft recipients are not severe, the short-term survival and the renal function of diabetic patients with end-stage renal disease improves after kidney-alone transplantation, which is still the standard method of treatment in Japan.

Adult↗
PubMed1997

[Dictyostelium].

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Animals↗
PubMed1996

Intracellular free calcium responses during chemotaxis of Dictyostelium cells.

A calcium ion indicator, fura-2 bovine serum albumin, was introduced into Dictyostelium discoideum cells by electroporation. The concentration of intracellular calcium ions ([Ca2+]i) increased transiently in vegetative cells upon stimulation with submicromolar concentrations of folic acid, a chemoattractant for this organism at the vegetative stage. Similar [Ca2+]i responses were also observed in aggregation-competent cells upon stimulation with subnanomolar concentrations of cAMP, a chemoattractant at the aggregation stage. The [Ca2+]i response caused by cAMP was 2.1 times higher than that caused by folic acid. The magnitude of these responses depended on the concentration of Ca2+ in the external buffer. The presence of magnesium ions inhibited the [Ca2+]i responses in a dose-dependent manner. [Ca2+]i was higher in the rear region than in the anterior region of cells freely migrating on the surface, although such a gradient was not always maintained. When aggregation competent cells were locally stimulated by the application of a microcapillary containing cAMP, the cells extended pseudopods toward the microcapillary. In these cases, an increase in [Ca2+]i was transiently observed in the region opposite to the tip of the capillary. At the slug stage, [Ca2+]i was higher in prestalk cells than in prespore cells of slugs. The possibility that the [Ca2+]i is spatially regulated within a cell was discussed.

Animals↗
PubMed1994

Intracellular free calcium level and its response to cAMP stimulation in developing Dictyostelium cells transformed with jellyfish apoaequorin cDNA.

A new method is described for measuring intracellular free calcium concentrations, [(Ca2+)i], in the cells of Dictyostelium discoideum transformed with apoaequorin cDNA of the jellyfish, Aequorea victoria. Aequorin, a calcium-specific indicator, was regenerated in vivo from apoaequorin produced in the cells by incubation with coelenterazine. The results showed that [(Ca2+)i] in developing cells markedly increases at the aggregation stage and again at the culmination stage after a temporary drop at the migration stage. Except for the vegetative stage, the cells at all stages of development exhibit a sharp transient increase in [(Ca2+)i] upon stimulation with a cAMP (50 nM) pulse, high responses being observed at the migration and culmination stages. Separated prestalk cells of migrating slugs contain more than twice as much [(Ca2+)i] and show three times as large a response to cAMP stimulation as prespore cells.

Aequorin↗
PubMed1994

Cell-cycle-dependent sorting in the development of Dictyostelium cells.

The sorting behavior of Dictyostelium discoideum Ax-2 cells and its relation to the cell-cycle phase at the onset of starvation were analyzed with reference to pattern formation, using beta-galactosidase as a cell marker and the temperature-shift method for cell synchronization. Cells transformed with the vector pAct15-Gal showed different sorting behavior during development when they were starved at different cell-cycle phases. Cells (T7) starved at the mid-late G2 phase (just before the PS-point from which cells enter the differentiation phase when starved) aggregated most rapidly and possibly functioned as aggregation centers, but were eventually sorted out to the posterior zone of migrating slugs. In contrast, T1 cells starved at the late G2 phase (just after the PS-point) exhibited slower aggregation compared with T7 cells. During further culture, T1 cells then sorted out to the apical tips of tipped aggregates and were located predominantly in the anterior zone of migrating slugs. Thus, T1 and T7 cells apparently interchange their positions in the cell masses during tip formation. The possible significance of cell-cycle-related sorting presented here is discussed, with special emphasis on pattern formation and cell differentiation.

Animals↗
PubMed1994

Cooperation of positively and negatively acting promoter elements determines prespore-specific transcription of Dp87 gene in Dictyostelium.

Dp87 gene in Dictyostelium is a novel prespore-specific gene, whose expression is first observed when the aggregation stream is formed, the earliest among prespore-specific genes so far isolated. By 5'-sequential deletion analyses, we had previously indicated that the region between -447 and -356 is important for transcription. Here we show by detailed analyses that the regulatory mechanism of the gene is more complex in that multiple positive and negative regulatory regions including the previously identified region act cooperatively. In addition, we show that the region including the putative TATA box and the transcriptional start site is required for proper negative regulation of the gene.

Animals↗
PubMed1994

Dictyostelium prespore-specific gene Dp87 encodes a sorus matrix protein.

In this paper we report on the characteristics of the product of a prespore-specific gene (Dp87) of Dictyostelium discoideum. Polyclonal antibody was made against a bacterially synthesized Dp87-encoded protein fragment. Using this antibody, the product was characterized by immunochemical and immunocytological methods. It was shown that the Dp87-encoded protein is a prespore-specific protein with a molecular mass of 83 kDa, which first appears at the standing slug stage and persists in mature fruiting bodies. Western blot studies revealed the presence of an additional 81 kDa protein prior to the appearance of the 83 kDa protein from the tipped aggregate to the standing slug stage, thus indicating the former to be a precursor protein. Immunocytochemical and immunoelectron microscopic studies showed that the protein is bound to ER at the early stages of development when only the 81 kDa protein is present. At the later stages when the 83 kDa protein predominates, however, it becomes localized in prespore-specific vacuoles (PSVs) and is associated with the inner fibrous material of PSVs, but not with the peripheral membranous material. This is in contrast to spore coat proteins, which are localized in PSVs from the beginning of their appearance and associated with both structures of PSVs. In mature fruiting bodies, most Dp87 protein is localized to the interspore space (matrix) of the sori, with some left on the surface of the stalk tube. Disruptants of the Dp87 gene were also produced. Although they contained neither 81 kDa nor 83 kDa protein, they showed no phenotypic defects as compared to the parental strain.

Animals↗
PubMed1994

Regulation of cell differentiation and pattern formation in Dictyostelium development.

Free-living cells of Dictyostelium discoideum aggregate to form a slug-shaped cell mass and differentiate into prestalk and prespore cells. The differentiation of prespore cells is characterized by expression of Dp87 gene, the earliest event of prespore differentiation. It encodes a protein which first appears in ER of aggregating cells in a precursor form, is then translocated to prespore vacuoles and modified to a mature form and finally exocytosed to constitute the sorus matrix. The transcription of Dp87 is regulated by the cis-acting region consisting of positive, prespore-specific, negative, non-prespore-specific and positive, cell-type-non-specific elements. Cells expressing Dp87 appear at random in early aggregation streams and centers and then sort out to the posterior part of the slug. Intercellular signals required for prestalk and prespore differentiation were investigated by incubation at a low cell density of disaggregated cells. cAMP is inhibitory at the first and second stages of prespore differentiation, while it is required at the third stage. The stalk differentiation is divided into four stages: cAMP is required at the second stage and differentiation inducing factor (DIF) at the third stage, where a low molecular weight secretory substance is also required. At the third stage, cAMP inhibits both ecmA and ecmB expression, while 8-Br-cAMP specifically induces ecmB and maturation of prestalk to stalk cells. The relationship between the differentiation tendency of preaggregative cells and the cell-cycle phase at the initiation of development was studied by the use of cells synchronized for growth by a temperature-shift method.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗