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JaLCDOI 10.18926/AMO/30846
FullText URL fulltext.pdf
Author Suwa, Kiichi|
Abstract

The relationship between alveolar macrophages and spheroid alveolar epithelial cells was studied with the electron microscope after injection of squid-ink solution into the trachea of the mouse. At 20 hours after injection of squid-ink solution slight degeneration was evident in alveolar macrophages with sepia-melanin particles being phagocytized with partial digestion by lysosmes. Furthermore, hardly any changes were seen in mitochondria and inclusion bodies of the spheroid alveolar epithelial cells. In contrast, at one week after injection of squid-ink solution, almost all alveolar macrophages were degenerated with destruction of the ectoplasm in which the ingested sepia-melanin particles were digested by lysosomes into fine particles, and the mitochondria of spheroid alveolar epithelial cells were degenerated and the inclusion bodies were hardly formed. At three weeks after injection of squid-ink solution, alveolar macrophages as well as speroid alveolar epithelial cells showed almost complete recovery of functional structure. As the phagocyte in the alveolar space, neutrophile leucocytes were also observed in addition to the so-called alveolar macrophage.

Amo Type Article
Publication Title Acta Medica Okayama
Published Date 1977-02
Volume volume31
Issue issue1
Publisher Okayama University Medical School
Start Page 15
End Page 34
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
File Version publisher
Refereed True
PubMed ID 140589
NAID 120002305572
Author Aisaka, Tadakazu|
Published Date 1962-09-30
Publication Title 岡山医学会雑誌
Volume volume74
Issue issue8-9
Content Type Journal Article
Author Tawara, Jutaro|
Published Date 1968-08-30
Publication Title 岡山医学会雑誌
Volume volume80
Issue issue7-8
Content Type Journal Article
Author Miwa, Yasuhiko|
Published Date 1967-12-30
Publication Title 岡山医学会雑誌
Volume volume79
Issue issue11-12
Content Type Journal Article
Author Suwa, Kiichi|
Published Date 1976-08-30
Publication Title 岡山医学会雑誌
Volume volume88
Issue issue7-8
Content Type Journal Article
Author Taguchi, Hirokuni| Sanada, Hiroshi| Tanaka, Toshio| Hayashi, Takehiko| Miyoshi, Isao| Kitayama, Minoru|
Published Date 1975-10-30
Publication Title 岡山医学会雑誌
Volume volume87
Issue issue9-10
Content Type Journal Article
Author Tomoyasu, Satoshi|
Published Date 1975-04-30
Publication Title 岡山医学会雑誌
Volume volume87
Issue issue3-4
Content Type Journal Article
Author Akatsuka, Kazuya|
Published Date 1978-04-30
Publication Title 岡山医学会雑誌
Volume volume90
Issue issue3-4
Content Type Journal Article
JaLCDOI 10.18926/15254
Title Alternative ヒスチジンタグを持つホスファカンコア蛋白の大腸菌での発現と精製
FullText URL 009_2_105_111.pdf
Author Ito, Sekiko| Okamoto, Motoi| Mori, Shuji|
Abstract Specific regions of core protein of phosphacan, one of the chondroitin sulfate proteoglycans, were expressed as fusion proteins with histidine-tag (His-tag) in Escherichia coli (E.coli) and were affinity purified using nickel-nitrilotriacetic acid (Ni-NTA) matrix. cDNA fragments encoding amino acid residues 343-446 (P3) and 1-340 (P4) of phosphacan core protein were amplified by polymerase chain reaction from E18 rat brain mRNA as template. The amplified products were subcloned into pQE30 vector and were introduced into E.coli strain M15 [pREP4] for the expression. The His-tagged fusion proteins were expressed by cultivating the transformants at 37℃ for 5h in the presence of 1mM IPTG. His-tagged P3 fusion protein (His-P3) was expressed as soluble form, and was purified using Ni-NTA matrix. His-tagged P4 fusion protein (His-P4) which was sequestered into insoluble inclusion bodies was treated with 8.0M urea to solubilize, and then was purified under denaturing conditions.
Keywords phosphacan (ホスファカン) core protein (コア蛋白) His-tagged proteins recombinant protein (融合蛋白)
Publication Title 岡山大学医療技術短期大学部紀要
Published Date 1999-02-26
Volume volume9
Issue issue2
Start Page 105
End Page 111
ISSN 0917-4494
language English
File Version publisher
NAID 120002307302
Author Kuyama, Keisuke|
Published Date 1991
Publication Title 岡山医学会雑誌
Volume volume103
Issue issue11-12
Content Type Journal Article
Author Shibata, Jun|
Published Date 1966-06-30
Publication Title 岡山医学会雑誌
Volume volume78
Issue issue6
Content Type Journal Article
Author Shibata, Jun|
Published Date 1966-06-30
Publication Title 岡山医学会雑誌
Volume volume78
Issue issue6
Content Type Journal Article
Author Ikeda, Kazuhiko|
Published Date 1966-06-30
Publication Title 岡山医学会雑誌
Volume volume78
Issue issue6
Content Type Journal Article
Author Yamamoto, Masakazu|
Published Date 1966-05-30
Publication Title 岡山医学会雑誌
Volume volume78
Issue issue4-5
Content Type Journal Article
Author Oda, Teruyuki|
Published Date 1991
Publication Title 岡山医学会雑誌
Volume volume103
Issue issue11-12
Content Type Journal Article
Author 横田 修| 寺田 整司| 石津 秀樹| 黒田 重利|
Published Date 2004-09-30
Publication Title 岡山医学会雑誌
Volume volume116
Issue issue2
Content Type Journal Article
Title Alternative Ixia から分離された bean yellow mosaic virus
FullText URL 004_002_201_213.pdf
Author Tsuji, Toshiya| Maeda, Takanori| Kondo, Hideki| Inouye, Narinobu|
Abstract A strain (Ixia-B) of bean yellow mosaic virus (BYMV) isolated from Ixia hybrida was characterized and compared with other isolates of BYMV and clover yellow vein virus (CYVV). Ixia-B was transmitted by aphids,Myzus presicae in a non-presistent manner and by sap-inoculation to 11 of 46 species in 5 of 10 families tested, and had a similar host range to that of some BYMV isolates, althrough some defferences were detected. Sap from diseased C. quinoa was infective after 10 min heating at 55℃ but not 60℃, after a dilution to 10-3 but not 10-4, and after 2 days but not 4 days at 20℃.The Virus particles were filamentous rods of about 13×820 nm. Ixia-B contaied a single protein species with a molecular weight of 34,000 and a single viral RNA with approximately 9,000 bases. In ultrahtin sections of leaf tissues from infected plants, the virus particles, cylindrical cytoplasmic inclusions and dense bodies were obsserved in the cytoplasm. The antiserum to Ixia-B produced by immunizing a rabbit had a titer of 1/512. A close serological relationship was revealed between Ixia-B and two strains of BYMV from crocus and gladiolus, but no relationship to clover yellow vein virus was found in agar gel diffusion tests. However,Ixia-B could be distinguished from two strains of BYMV by the formation of spurs among them in agar gel and by the differences in the patterns of peptide mapping of coat proteins. From these findings, Ixia-B was identified as a strain of BYMV.
Keywords Ixia hybrida Bean yellow mosaic virus Potyvirus
Publication Title 岡山大学資源生物科学研究所報告
Published Date 1996
Volume volume4
Issue issue2
Start Page 201
End Page 213
ISSN 0916-930X
language English
File Version publisher
NAID 120002313395
Author Francico Javier Diaz Corrales|
Published Date 2006-03-24
Publication Title
Content Type Thesis or Dissertation
FullText URL O003631.pdf
Author 寺田 整司|
Published Date 2001-09-30
Content Type Thesis or Dissertation
Grant Number 乙第3631号
Granted Date 2001-09-30
Thesis Type Doctor of Philosophy in Medical Science
Grantor 岡山大学
language Japanese