Researcher Profile and Settings

Master

Affiliation (Master)

• Faculty of Medicine　Institute for Animal Experimentation

Affiliation (Master)

• Faculty of Medicine　Institute for Animal Experimentation

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Profile and Settings

Profile and Settings

• Name (Japanese)

  Tosa

• Name (Kana)

  Noriko

• Name

  201301072780801915

Alternate Names

http://kaken.nii.ac.jp/d/r/20312415.ja.html

Achievement

Research Areas

• Life sciences / Laboratory animal science

Research Experience

• 2009/04 - Today Hokkaido University Institute for Animal Experimentation, Faculty of Medicine Assistant Professor

Awards

• 2023/09 Asian Federation of Laboratory Animal Science Assosiations The 9th AFLAS Congress 2023 Travel Award
   Analysis of storage and transport conditions of multiplex ICG sticks for diagnosis of infectious diseases in rats and mice 

  受賞者: Noriko Tosa
• 2013/05 日本実験動物技術者協会 第4回実験動物福祉奨励賞
   マウスの被毛異常または床敷湿潤が発生した後の環境エンリッチメントの効果 

  受賞者: 土佐 紀子

Published Papers

• Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay.

  Tosa N, Ishida T, Yoshimatsu K, Hayashimoto N, Shiokawa K, Takakura A, and Arikawa J

  Exp. Anim. 70 (2) 161 - 168 2021/05 [Refereed][Not invited]
  
• Multiplex Immunochromatographic Assay for Serologic Diagnosis of Major Infectious Diseases in Laboratory Mice.

  Noriko Tosa, Tomoko Ishida, Kumiko Yoshimatsu, Nobuhito Hayashimoto, Kanae Shiokawa, Akira Takakura, Jiro Arikawa

  Journal of the American Association for Laboratory Animal Science : JAALAS 58 (6) 790 - 795 2019/11/01 [Refereed]
   

  Serologic monitoring of infectious diseases is important for microbial control in colonies of laboratory mice. Rapid and simple tests that do not require killing animals are valuable for this purpose. In this study, we developed a multiplex immunochromatographic assay (ICA) for detection of antibodies to mouse hepatitis virus (MHV), Sendai virus (also known as hemagglutinating virus of Japan [HVJ]), and Clostridium piliforme (The pathogen that causes Tyzzer disease), which are major infectious diseases in mice. For this assay, an ICA strip was put into a microtube containing 150 μL PBS and either 0.75 μL mouse serum or 1.5 μL whole blood. Binding antibodies were visualized by using protein A-conjugated colloidal gold. Under these conditions, multiplex ICA simultaneously and specifically detected antibodies to multiple antigens. To evaluate the sensitivity and specificity of multiplex ICA, positive serum samples for each infectious disease were used. Sensitivities of the multiplex ICA test for MHV, HVJ, and C. piliforme were 100%, 100%, and 90%, respectively. No nonspecific reaction was observed in any of the 30 positive sera. In addition, 10 samples of uninfected sera did not show any bands except for the control line. These observations indicate high specificity of the multiplex ICA test. Moreover, the multiplex ICA could be applied to diluted blood. These results indicate that the multiplex ICA is appropriate for rapid, simple, and safe serologic testing of laboratory mice.
• Comparison of immune response in mice sensitized to an animal allergen, Can f 1, and to a food allergen, ovalbumin

  Noriko Tosa, Kumiko Yoshimatsu, Motoko Takahashi, Jiro Arikawa

  Biomedical Research 40 (1) 9 - 15 2019 [Refereed][Not invited]
   

  Can f 1 belongs to the lipocalin superfamily and is considered to be an animal allergen. The immune response induced by Can f 1 in mice was compared with that induced by ovalbumin (OVA), a typical food allergen. Female BALB/c and C57BL/6 mice (6 weeks of age) were subcutaneously injected with Can f 1 or OVA with or without aluminum hydroxide (Alum) three times with intervals of two weeks. Serum levels of total IgE or antigen-specific IgE and production of IL13 and IFNγ from splenocytes were analyzed. Immunization with Can f 1 or OVA increased serum levels of both total IgE and antigen-specific IgE significantly irrespective of Alum. These results indicate that Can f 1 and OVA were able to induce allergic sensitization in mice. Splenocyte production of IL13 in mice immunized with Can f 1 or OVA with and without Alum were significantly increased after stimulation with each antigen. However, IL13 levels in the mice immunized with Can f 1 with Alum were significantly lower than those immunized without Alum. Increases in IFNγ levels after stimulation with Can f 1 or OVA were not remarkable. No influence of genetic backgrounds of BALB/c and C57BL/6 mice was found. Although Can f 1 induced Th2 type immune responses as was also the case for immunization with OVA, an inhibitory effect of Alum on induction of IL13 was observed only in mice immunized with Can f 1. These results suggest that the immune mechanism for allergic sensitization with Can f 1 is different from that with OVA.
• Variation in the bacterial conditions inside cages is correlated with intracage humidity and ammonia levels.

  Tosa N, Yoshimatsu K, Tadasuke Tsukiyama, Hatakeyama S, Arikawa J

  Lab Animal and Environ 21 (2) 87 - 98 2013 [Refereed][Not invited]
  
• Environmental enrichment after the occurrence of wet bedding and the appearance of abnormal fur in mice is effective for solving those problems

  TOSA Noriko, YOSHIMATSU Kumiko, ARIKAWA Jiro

  Lab Animal and Environ 20 (1) 1 - 8 1342-2731 2012 [Refereed][Not invited]
  
• Effect of environmental enrichment after the occurrence of wet bedding created by mice and abnormal fur in mice.

  Tosa N, Yoshimatsu K, Arikawa J

  J Am Assoc Lab Anim Sci 50 (5) 779 - 780 2011/09 [Refereed][Not invited]
  
• Rab7 is a critical mediator in vesicular transport of tyrosinase-related protein 1 in melanocytes

  Tokimasa Hida, Hitoshi Sohma, Yasuo Kokai, Akinori Kawakami, Kuninori Hirosaki, Masae Okura, Noriko Tosa, Toshiharu Yamashita, Kowichi Jimbow

  JOURNAL OF DERMATOLOGY 38 (5) 432 - 441 0385-2407 2011/05 [Refereed][Not invited]
   

  How melanosomal proteins such as enzymic proteins (tyrosinase and tyrosinase-related proteins, Tyrps) and structural protein (gp100) are transported from Golgi to melanosomal compartments is not yet fully understood. A number of small GTPases have been found to be associated with melanosomes and we have identified one of them, Rab7, a regulator of vesicular transport, organelle motility, phospholipid signaling and cytosolic degradative machinery, as being involved in the transport of Tyrp1 from Golgi to stage I melanosomes. This study further characterizes the role of Rab7 as a regulator of differential sorting of melanosomal proteins in this process. Murine melanocytes were transiently transfected with a plasmid encoding either wild-type (Rab7WT), constitutively active (Rab7Q67L) or dominant-negative (Rab7N125I and Rab7T22N) Rab7. Through immunocytostaining and confocal laser scanning microscopy, we quantitatively compared the bio-distribution of melanosomal proteins between Rab7WT-expressing cells and mutant Rab7-expressing cells. We also characterized their differential elimination from melanosomal compartments by Rab7 by utilizing a proteasome inhibitor, MG132. Our findings indicate that Rab7 plays an important role in differential sorting of tyrosinase, Tyrp1 and gp100 in early melanogenesis cascade, and that it is more specifically involved with Tyrp1 than tyrosinase and gp100 in the trafficking from Golgi to melanosomes and the specific exit from the degradative process.
• Critical function of death-associated protein 3 in T cell receptor-mediated apoptosis induction

  Noriko Tosa, Atsushi Iwai, Taku Tanaka, Tomoka Kumagai, Takeshi Nitta, Satoko Chiba, Masahiro Maeda, Yousuke Takahama, Toshimitsu Uede, Tadaaki Miyazaki

  BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 395 (3) 356 - 360 0006-291X 2010/05 [Refereed][Not invited]
   

  Death-associated protein 3 (DAP3) is crucial for promoting apoptosis induced by various stimulations. This report demonstrates that DAP3 is also important for T cell receptor (TCR)-mediated apoptosis induction in immature thymocytes. Enforced expression of DAP3 accelerated the negative selection in developing thymocytes, using the reaggregate thymus organ culture system. In addition, expression of DAP3 accelerated TCR-mediated apoptosis induction in DO11.10 cells. We also demonstrated that DAP3 translocates into the nucleus during TCR-mediated apoptosis in a Nur77 dependent manner. It is concluded that DAP3 is critical for TCR-mediated induction of apoptosis at the downstream of Nur77. (C) 2010 Elsevier Inc. All rights reserved.
• Functional role of death-associated protein 3 (DAP3) in anoikis

  T Miyazaki, M Shen, D Fujikura, N Tosa, HR Kim, S Kon, T Uede, JC Reed

  JOURNAL OF BIOLOGICAL CHEMISTRY 279 (43) 44667 - 44672 0021-9258 2004/10 [Refereed][Not invited]
   

  Detachment of adherent epithelial cells from the extracellular matrix induces apoptosis, known as anoikis. Integrin stimulation protects cells from anoikis, but the responsible mechanisms are not well known. Here, we demonstrated that a pro-apoptotic GTP-binding protein, DAP3 (death-associated protein 3), is critical for induction of anoikis. Down-regulation of DAP3 expression by antisense oligonucleotides inhibited anoikis. Conversely, overexpression of DAP3 augmented cell death and caspase activation induced by cell detachment. Furthermore, the association of DAP3 with FADD and the activation of caspase-8 were induced by cell detachment. We also showed that DAP3 is phosphorylated by kinase Akt (PKB), and active Akt can nullify apoptosis induction by DAP3. Mutation of a consensus Akt phosphorylation site in DAP3 renders it resistant to suppression by active Akt in cells. Integrin ligation stimulates Akt activation and phosphorylation of DAP3 in intact cells, as well as suppresses the ability of DAP3 overexpression to augment anoikis. Involvement of DAP3 in anoikis signaling demonstrates a novel role for this GTP-binding protein in apoptosis induction caused by cell detachment.
• Functional role of DAP(death associated protein)3 in apoptosis induction

  Miyazaki F, Shen M, Tosa N, Fujikura D, Kon S, Uede T, Reed JC

  FASEB JOURNAL 18 (4) A42  0892-6638 2004/03/23 [Refereed][Not invited]
  
• Critical function of T cell death-associated gene 8 in glucocorticoid-induced thymocyte apoptosis

  N Tosa, M Murakami, WY Jia, M Yokoyama, T Masunaga, C Iwabuchi, M Inobe, K Iwabuchi, T Miyazaki, K Onoe, M Iwata, T Uede

  INTERNATIONAL IMMUNOLOGY 15 (6) 741 - 749 0953-8178 2003/06 [Refereed][Not invited]
   

  Transcriptional expression of a gene or genes is absolutely required for induction of glucocorticold-induced thymocyte apoptosis. We have previously shown that expression of T cell death-associated gene 8 (TDAG8) is quickly induced exclusively in the thymus after dexamethasone (DEX) treatment. Here, we present data that TDAG8 expression is induced prior to induction of DEX-mediated apoptosis. In contrast, TDAG8 expression in thymocytes was not induced in the process of gamma-irradiation-mediated apoptosis. TDAG8 expression accelerated only DEX-induced, but not TCR-mediated or gamma-irradiation-induced, thymocyte apoptosis in transgenic mice overexpressing TDAG8. Interestingly, these effects were specifically detected in CD4(+)CD8(+) double-positive thymocytes. Moreover, activation of caspase-3, -8 and -9 was enhanced in thymocytes of TDAG8 transgenic mice after DEX stimulation. In conclusion, TDAG8 expression is involved in glucocorticold-induced signals to activate caspase-9, -8 and -3 for subsequent apoptosis induction in CD4(+)CD8(+) double-positive thymocytes.
• Defective development of NK1.1+ T-cell antigen receptor + cells in zeta-associated protein 70 null mice with an accumulation of NK1.1+ CD3- NK-like cells in the thymus.

  Iwabuchi K, Iwabuchi C, Tone S, Itoh D, Tosa N, Negishi I, Ogasawara K, Uede T, Onoe K

  Blood 91 (6) 1765 - 1775 2001 [Refereed][Not invited]
  
• Involvement of CD28/CTLA4-B7 costimulatory pathway in the development of lymphadenopathy and splenomegaly in MRL/lpr mice

  M Takiguchi, M Murakami, Nakagawa, I, MM Rashid, N Tosa, S Chikuma, A Hashimoto, T Uede

  JOURNAL OF VETERINARY MEDICAL SCIENCE 62 (1) 29 - 36 0916-7250 2000/01 [Refereed][Not invited]
   

  MRL/lpr mouse is an established animal model which develops autoimmune diseases including glomerulonephritis, sialoadenitis, hepatitis and inflammatory lung disease. Additionally, it has been reported that lpr strains uniquely accumulate CD3(+)CD4(-)CD8(-)B220(+) (double negative, DN) T cells in lymphoid organs leading to lymphadenopathy and splenomegaly. To investigate the role of CD28/CTLA4-B7 pathway in the development of lymphadenopathy and splenomegaly, MRL/lpr mice were treated with soluble form of CTLA4 molecules. CTLA4IgG, which efficiently blocks this pathway. It was demonstrated that (i) the development of DN T cells was independent of the CD28/CTLA4-B7 pathway, (ii) the CD28/CTLA4-B7 pathway was required for the development of lymphadenopathy and splenomegaly, (iii) the CD28/CTLA4-B7 pathway was important for the accumulation of various cell populations in the lymph node and spleen, (iv) composition of the accumulating cell populations was not altered by CTLA4IgG treatment, and (v) activation of conventional T cells and IL-4 production from conventional T cells were the CD28/CTLA4-B7 pathway dependent. Thus, we concluded that the CD28/CTLA4-B7 pathway was required for the development of full-blown lymphadenopathy and splenomegaly in MRL/lpr mice.
• Detection of various epitopes of murine osteopontin by monoclonal antibodies

  H Hotta, S Kon, YU Katagiri, N Tosa, T Tsukamoto, AF Chambers, T Uede

  BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 257 (1) 6 - 11 0006-291X 1999/04 [Refereed][Not invited]
   

  We immunized rats with recombinant murine osteopontin protein and obtained four monoclonal antibodies recognizing distinct epitopes of murine osteopontin. OPN1.2 recognized the amino-terminal half of OPN, while OPN2.2, OPN2.3, and OPN3.1 recognized the carboxy-terminal half of OPN. The epitope recognized by OPN2.2 was destroyed by further cleavage of the carboxy half of OPN. The epitope recognized by OPN2.3 was located in the amino-terminal end of the carboxy half of OPN, whereas that recognized by OPN3.1 was located in the carboxy-terminal end of the carboxy half of OPN. OPN1.2 and OPN2.2 recognized thrombin-cleaved osteopontin, whereas thrombin-cleaved osteopontin was not recognized by OPN2.3 and OPN3.1. Thus, these monoclonal antibodies will be useful in structure/function studies of the role of osteopontin in murine models of disease. (C) 1999 Academic Press.
• Haptoglobin in Carnivora: a unique molecular structure in bear, cat and dog haptoglobins.

  K Mominoki, N Nakagawa-Tosa, M Morimatsu, B Syuto, M Saito

  Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology 110 (4) 785 - 9 1096-4959 1995/04 

  Haptoglobin (Hp), a hemoglobin-binding protein in plasma, consists of alpha and beta subunits and has a tetra-chain arrangement (beta-alpha-alpha-beta) connected by disulfide bridges in most mammals so far examined. Dog Hp has been reported to be unique compared with other Hps in respect that (1) the two alpha beta units are joined by a non-covalent interaction rather than a disulfide bridge and (2) the alpha chain has an oligosaccharide-binding sequence (Asn-X-Ser/Thr) and is glycosylated. To determine whether the unique structures of dog Hp are common in the Carnivora, we purified Hps from sera of bear and cat, and analyzed their subunit structure and partial amino acid sequences. The analyses by gel filtration and sodium dodecyl sulfate-polyacrylamide gel electrophoresis, under both reducing and non-reducing conditions, revealed that bear and cat Hps have similar subunit arrangements to dog Hp, suggesting the absence of a disulfide bridge between two alpha chains. This was confirmed by amino acid sequence analysis of the alpha chains: that is, Cys15 participating in the inter-alpha chain disulfide bridge was replaced by Val in bear or Leu in cat and dog. Thus, the unique subunit arrangement of Hp reported in dog may be common in the Carnivora. In contrast to dog Hp, however, alpha chains of bear and cat Hps were found not to have the typical oligosaccharide binding sequence on their alpha chains and were not glycosylated.
• HAPTOGLOBIN IN CARNIVORA - A UNIQUE MOLECULAR-STRUCTURE IN BEAR, CAT AND DOG HAPTOGLOBINS

  K MOMINOKI, N NAKAGAWATOSA, M MORIMATSU, B SYUTO, M SAITO

  COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY 110 (4) 785 - 789 0305-0491 1995/04 [Refereed][Not invited]
   

  Haptoglobin (Hp), a hemoglobin-binding protein in plasma, consists of alpha and beta subunits and has a tetra-chain arrangement (beta-alpha-alpha-beta) connected by disulfide bridges in most mammals so far examined, Dog Hp has been reported to be unique compared with other Hps in respect that (1) the two alpha beta units are joined by a non-covalent interaction rather than a disulfide bridge and (2) the alpha chain has an oligosaccharide-binding sequence (Asn-X-Ser/Thr) and is glycosylated, To determine whether the unique structures of dog Hp are common in the Carnivora, we purified Hps from sera of bear and cat, and analyzed their subunit structure and partial amino acid sequences, The analyses by gel filtration and sodium dodecyl sulfate-polyacrylamide gel electrophoresis, under both reducing and non-reducing conditions, revealed that bear and cat Hps have similar subunit arrangements to dog Hp, suggesting the absence of a disulfide bridge between two a chains, This was confirmed by amino acid sequence analysis of the alpha chains: that is, Cys(15) participating in the inter-a chain disulfide bridge was replaced by Val in bear or Leu in cat and dog, Thus, the unique subunit arrangement of Hp reported in dog may be common in the Carnivora, In contrast to dog Hp, however, alpha chains of bear and cat Hps were found not to have the typical oligosaccharide binding sequence on their alpha chains and were not glycosylated.
• STIMULATION OF HAPTOGLOBIN SYNTHESIS BY INTERLEUKIN-6 AND TUMOR-NECROSIS-FACTOR, BUT NOT BY INTERLEUKIN-1, IN BOVINE PRIMARY CULTURED-HEPATOCYTES

  N NAKAGAWATOSA, M MORIMATSU, M KAWASAKI, H NAKATSUJI, B SYUTO, M SAITO

  JOURNAL OF VETERINARY MEDICAL SCIENCE 57 (2) 219 - 223 0916-7250 1995/04 [Refereed][Not invited]
   

  The hepatic synthesis of acute phase proteins in ruminants has been suggested to be regulated by some mechanisms different from those in other species such as rodents and human. To explore possible regulatory factors unique to ruminants, we examined effects of interleukin (IL)-6, IL-1 and tumor necrosis factor (TNF), on haptoglobin (Hp) synthesis using a primary culture system of bovine hepatocytes. After bovine primary cultured hepatocytes were incubated in the presence of various concentrations of the cytokines, the synthesis and mRNA level of haptoglobin and albumin were measured by labeling with [S-35]-methionine and immunoprecipitation, and by Northern blot analysis, respectively. Hp synthesis was dose-dependently increased by recombinant human (rh) IL-6, and also by rhTNF-alpha, but to a less extent, while it was not affected by rhlL-1 beta. The stimulatory effect is mainly pretranslational, because mRNA level of Hp changed in parallel with protein synthesis. In contrast, albumin synthesis was suppressed by these three cytokines similarly. These results are inconsistent with the previously proposed view that TNF and IL-l overlap in their pathways leading to the transcriptional activation of many acute phase protein genes. In conclusion, there is a species-specific unique signaling system, especially for TNF, in transcriptional activation of bovine Hp gene.
• ISOLATION AND PRIMARY CULTURE OF BOVINE HEPATOCYTES - ALBUMIN SYNTHESIS AND ADRENERGIC ACTIVATION OF GLYCOGENOLYSIS

  N NAKAGAWATOSA, M MORIMATSU, K MOMINOKI, H NAKATSUJI, B SYUTO, M SAITO

  JOURNAL OF VETERINARY MEDICAL SCIENCE 56 (1) 125 - 129 0916-7250 1994/02 [Refereed][Not invited]
   

  We describe a technique for isolation and primary culture of bovine hepatocytes, and their metabolic characterization. Hepatocytes were isolated from the caudate lobe of bovine liver by perfusion with 0.25 mM ethyleneglycol tetraacetic acid and 0.05% collagenase. The viability and yield of the cells were 70-92% and 0.1-3.6 x 10(7) cells/g liver, respectively. When the isolated hepatocytes were cultured in Williams' medium E, they began to spread in 3 hr and formed monolayers in 24 hr. These monolayers were retained for at least 6 days. To monitor the metabolic activities specific to liver, synthesis and secretion of albumin were measured by labeling with [S-35]-methionine and immunoprecipitation. This activity was low in isolated hepatocytes, but increased after culturing 1-3 days, and decreased again after 6 days. Glycogenolytic activity was also assessed by measuring glucose release to the medium by stimulation with epinephrine. The glycogenolytic response to epinephrine was also enhanced by culturing the hepatocytes 1-3 days, but was decreased after 6 days. Since the isolated bovine hepatocytes retained the liver-specific activities of albumin synthesis and glycogenolysis for several days in culture, these cells are useful for cellular and molecular studies on the functions of bovine liver.
• PURIFICATION AND IDENTIFICATION OF A SERUM-PROTEIN INCREASED BY ANTHELMINTIC DRUGS FOR DIROFILARIA-IMMITIS IN DOGS

  N TOSA, M MORIMATSU, M NAKAGAWA, F MIYOSHI, E UCHIDA, M NIIYAMA, B SYUTO, M SAITO

  JOURNAL OF VETERINARY MEDICAL SCIENCE 55 (1) 27 - 31 0916-7250 1993/02 [Refereed][Not invited]
   

  Polyacrylamide gel electrophoretic analysis of canine serum protein has revealed that the administration of anthelmintics elicits an increase in a certain serum protein. This protein, named PT60, was partially purified by ammonium sulfate fractionation and preparative electrophoresis. The purified PT60 gave a single band with the molecular size of 53 kDa in sodium dodecyl sulfate-polyacrylamide gel electrophoresis under non-reducing conditions. After reduction with 2-mercaptoethanol, two bands appeared at 35 kDa and 17 kDa, indicating that PT60 consists of two subunits which are linked with each other by disulfide bonds. PT60 had the capacity to bind to hemoglobin. In an immunodiffusion test, an antiserum against PT60 cross-reacted with canine haptoglobin (Hp). N-terminal amino acid sequences of two PT60 subunits were identical to those of alpha and beta subunits of canine Hp, respectively. Thus, PT60 was identified as Hp.

MISC

• コモンマーモセットの飼育管理における試行錯誤 ～個性豊かなマーモセットたちと向き合って～

  土佐紀子  日本実験動物技術者協会北海道支部会誌  45-  2022/04  [Invited]
  
• コモンマーモセット飼育室の稼働 ～沢山の方たちに助けて頂いて～

  土佐紀子  日本実験動物技術者協会北海道支部会誌  44-  6  -10  2021/04  [Not refereed][Invited]
  
• プロポロリスコーティング床敷はケージ内常在菌の増殖とマウスアレルゲンの発生を抑制する

  TOSA NORIKO, YOSHIMATSU, KUMIKO, TSUKIYAMA TADAYUI, HATAKEYAMA SHIGETSUGU, ARIKAWA JIRO  日本実験動物学会総会講演要旨集  61st-  280  2014/05/01  [Not refereed][Not invited]
  
• DAP3(death associated protein 3)を介するアポトーシスシグナルの解明

  宮崎忠昭, SHEN M, 藤倉大介, 土佐紀子, 今重之, 上出利光, REED J  日本分子生物学会年会プログラム・講演要旨集  27th-  2004
• Functional role of DAP3 (death associated protein 3) in anoikis

  T Miyazaki, M Shen, N Tosa, S Kon, T Uede, JC Reed  FASEB JOURNAL  17-  (7)  C316  -C316  2003/04  [Not refereed][Not invited]
  
• アポトーシス誘導におけるDAP3の機能

  宮崎忠昭, CHEN M, 土佐紀子, 今重之, 上出利光, REED J  日本分子生物学会年会プログラム・講演要旨集  26th-  2003
• The functional analysis of DIG1 molecule, a putative G protein-coupled receptor, in dexamethasone-induced thymocyte apoptosis.

  N Tosa, M Murakami, M Iwata, WY Jia, M Yokoyama, K Iwabuchi, M Inobe, T Uede  FASEB JOURNAL  15-  (4)  A315  -A315  2001/03  [Not refereed][Not invited]
  
• 胸腺内NK-T細胞の分化経路

  岩渕和也, 岩渕千雅子, 刀祢さおり, 土佐紀子, 上出利光, 小野江和則  日本呼吸器外科学会雑誌  15-  (())  1  2001  [Not refereed][Not invited]
  
• Acute Phase Response of Haptoglobin in Cattle Assessed by a Single Radial Immunodiffusion Method.

  MORIMATSU MASAMI, TOSA NORIKO, NAIKI MASAHARU, SAITO MASAYUKI  家畜生化学研究会報  (29)  61  -68  1992/09  [Not refereed][Not invited]
  

Research Projects

• Development and Evaluation of Damage Control Resuscitation Training Curriculum for General Surgeons

  Japan Society for the Promotion of Science：Grants-in-Aid for Scientific Research

  Date (from‐to) : 2022/04 -2027/03 

  Author : 村上 壮一, 土佐 紀子, 方波見 謙一, 倉島 庸, 平野 聡, 本間 宙, 七戸 俊明, 伊澤 祥光
• Development of rapid and simple individeual diagnostic method for major infectious diseases in laboratory animals : a multiplex immunochromatographic test

  Japan Society for the Promotion of Science：Grants-in-Aid for Scientific Research

  Date (from‐to) : 2020/04 -2023/03 

  Author : 土佐 紀子, 林元 展人, 石田 智子, 森松 組子

   

  学術・科学技術の研究に供する動物の微生物モニタリングは、研究結果の信頼性の担保、および動物福祉の観点から必要不可欠である。近年、多系統少数個体維持の増加や個別換気型飼育機の普及等により、従来の微生物モニタリング方法、すなわち「おとり動物」の感染症の検出を指標とする間接的な方法では感染症を摘発することが困難となっている。この問題を解決するためには、動物を安楽死させることなく微量全血を用い、マウス、ラットの主要感染症を同時に且つ迅速・簡便に検出できる個体別血清診断法の確立が必要である。その方法として有望と考えられる「多項目イムノクロマト(ICG)法」の開発について申請者らは取り組んで来た。 本研究ではこれまでの成果を基に、１）多項目ICG法の検出条件が確定したマウス・ラットの感染症（マウス：マウス肝炎ウイルス感染症、センダイウイルス感染症、ティザー病。ラット：唾液腺涙腺炎ウイルス感染症、センダイウイルス感染症、腎症候性出血熱）の検出における本法の実用性を検証し、２）上記感染症に加え、主要感染症であるマイコプラズマ感染症（マウス、ラット）とティザー病（ラット）のICG法を確立することを目的としている。２年度（令和３年度）においては、以下の研究を実施した。 １．多項目ICGスティックの最適な保管条件・最長保管期間を明らかにする実験において、保管期間６ヶ月および１２ヶ月の多項目ICGスティックの各保管条件における検出・感度特異性への影響の結果を得た。 ２．乾燥血液を用いた時のICG法の検出・感度特異性を明らかにするため、乾燥血液を作製するための条件を検討した。 ３．多項目ICGスティックの輸送条件を確定するための実験設備の準備を行った。 ４．Myco（マウス、ラット）とTyzzer（ラット）のICG法を確立するため、抗原の準備を行い、ICGメンブレンに塗布する抗原処理方法の実験に着手した。
• Development of new DCS training course aiming at improving the survival rate of severe trauma patients in non-urban area

  Japan Society for the Promotion of Science：Grants-in-Aid for Scientific Research

  Date (from‐to) : 2016/04 -2020/03 

  Author : MURAKAMI SOICHI

   

  We contacted 117 trauma care specialists nationwide to cooperate in selecting trauma treatment skills that general surgeons should acquire, conducted a questionnaire survey using the Delphi method, and selected 35 items with Cronbach's alpha 0.94. We also conducted the survey for the experience and proficiency of the items on this list with 739 general surgeons in Hokkaido and analyzed 444 effective responses. Eight items, splenectomy, diaphragm injury repair, intraperitoneal gauze packing, liver injury gauze packing, suture for liver injury, hepatorrhaphy for liver injury, trauma laparotomy, Focused Assessment with Sonography for Trauma (FAST) were selected as training items. Based on this result, a new training course of trauma care that is optimized for general surgeons, using simulators, living pigs, cadavers, and e-learning was established.
• Analysis of the relationship between T cell repertory and incidence of laboratory animal allergy by environmental factors

  Japan Society for the Promotion of Science：Grants-in-Aid for Scientific Research

  Date (from‐to) : 2015/04 -2018/03 

  Author : Tosa Noriko

   

  In this study, exposure of antigens to fetus or juvenile mice suppressed the induction of laboratory animal allergy. These results suggest incidence of laboratory animal allergy is influenced by environmental factors and the relationship between the influence and establishment of T cell repertory as T cell repertory is established in fetus or juvenile mice. Moreover, animal allergen Can f 1-specific IgE and IL13 levels in the mice immunized with Can f 1 were influenced by aluminum hydroxide, differing from the results for immunization with OVA as a food allergen. These results suggest that the immune mechanism for laboratory animal allergy is different from that with food allergy.
• Studies on the immunochromatography for detecting antibody to major zoonoses and infectious diseases among laboratory rat and mouse.

  Japan Society for the Promotion of Science：Grants-in-Aid for Scientific Research

  Date (from‐to) : 2015/04 -2018/03 

  Author : ARIKAWA Jiro

   

  Immunochromatography test for detecting antibody against causative agents of diseases of laboratory rat (Sendai virus, Tyzzer’s disease, Mycoplasma, sialodacryoadenitis virus, hemorrhagic fever with renal syndrome) and laboratory mouse (mouse hepatitis, Sendai virus, Tyzzer’s disease, Mycoplasma) was developed by using extracted antigen or virus particle as antigens and Protein A labeled colloidal gold particle. Results with immune serum and rat and mouse sera collected from multiple animal facilities showed the sufficient specificity and sensitivity. Further, this immunochromatography test is available with diluted blood specimens. These results indicated that this immunochromatography test is rapid and sensitive serodiagnostic tool among laboratory mouse and rats.
• The role of DIG-1 gene steroid-induced apoptosis.

  Japan Society for the Promotion of Science：Grants-in-Aid for Scientific Research

  Date (from‐to) : 1998 -2000 

  Author : UEDE Toshimitsu, TOSA Noriko, IWATA Makoto

   

  1. We cloned and sequence a DIG-1 gene that specifically expressed by thymocytes after dexamethason(DEX)treatment. 2. DIG-1 gene encodes 7 transmembrane G protein coupled receptor. 3. We have established 3 lines of DIG-1 transgenic mice. 4. In transgenic mice, thymus were significantly smaller than those in control mice. After DEX injection, the apoptotic cells within thymic cortex increased siginificantly as compared to those in control mice. The apoptotic cells were mainly CD4+CD8+ thymocytes. 5. The expression of apoptosis-related proteins, Bcl-2 and BAX were not significantly different from thosse in transgenic mice.