• Applied Microscopy
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• 제9권1호
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• pp.87-94
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• 1979

• 한국잠사곤충학회지
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• 제18권2호
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• pp.1-60
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• 1976

본 연구에서는 전자현미경과 Radioautography에 의하여 가잠의 휴면 기구를 연구하였다. 1. 가잠의 휴면성은 최청중의 온도와 명장에 의하여 변하기 쉬운 것으로서 특히 배자의 후기와 관계가 깊다는 사실은 잘 알려저 있다. 그러므로 저온과 고온최청의 경우 가잠의 배자 발생 단계중에 있어서 핵산과 단백질의 전구물질을 사용하여 합성의 Pattern을 조사하였다. 고온최청 때에는 반전후 3일째에 $^3$H-glycine이 배자의 뇌와 식도하신경구에 다량으로 들어가 있는 동시에 타부위에도 약간이나마 들어가 있었다. 그러나 저온최청 때에는 뇌와 식도하신 경구 그리고 타부위 사이에 차이가 없었다. 고온과 저온과의 사이에는 배자의 DNA 합성의 차리를 인정할 수 없었다. 산난후 20일째의 휴면난에 있어서는 소수의 중배엽세포의 핵에 들어가 있었으나 월연한 잠난에 있어서는 중배엽의 전핵에 들어가 있었다. 고온과 저온최청때에 반전후의 배자의 전부 즉 뇌와 식도하신경구의 주위에만 $^3$H-thymidine이 들어가 있는 것을 볼 수 있었으나 후부에서는 전혀 볼 수 없었다. 한편 전 최청기간중 또는 산난후 20일째의 난황세포에 있어서는 단백질합성과 나NA 합성을 인정하지 못하였으나 월년난 배자의 부속지 발생전까지는 RNA합성이 관찰되었다.

• 치과방사선
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• 제13권1호
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• pp.75-85
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• 1983

Age differences in the skin structure have been studied in young (one year-old) and aged (five and a half year-old) frogs, Xenopus laevis. The epidermis in young frogs is made up of an average of 6.3 and 4.7 layers of epithelial cells at abdominal and dorsal surfaces, respectively. In aged frogs, the number of respective cell layers at abdominal and dorsal surfaces increases to 8.8 and 5.6. The thickness of the dermis (spongiosum) in aged frogs is decreased 25% on the abdominal side (from 267㎛ to 207㎛) but is increased by 11 % on the dorsal side (from 275㎛ to 305㎛). The nucleolar index and ³H-uridine incorporation, as judged by radioautography, by epithelial cells are drastically reduced in aged frogs.

• Applied Biological Chemistry
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• 제19권2호
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• pp.70-74
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• 1976

Thyroid hormone의 생합성반응기작을 알아보기 위하여 방사선 I-131을 쥐에 주사한 후 thyroid gland을 분리하여 분석하였다. Pancreatin viokase를 처리하여 분리한 요드화합물을 여지 크로마토그라피로 분리 동정하고 이를 radioautography로 분석한 결과 I-131은 주사후 바로 쥐의 체내에서 흡수되어 monoiodotyrosine이 되고 이것은 diiodotyrosine으로 전환됨을 관찰하였다. 실험결과는 diiodotyrosine은 thyroxine 생합성에 있어서 중간생성물이나 반면 triiodothyronine은 오히려 분해산물임을 보여 주었다. 또한 환원제인 propylthiouracil을 투여한 쥐에서 iodine의 체내집적현상(Iodine Pump)은 현저히 증가하였으나 유기 요도화합물을 전환되는 것을 저하였다.

• 대한치과의사협회지
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• 제10권9호
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• pp.587-592
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• 1972

• Applied Microscopy
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• 제22권2호
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• pp.118-126
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• 1992

The pathway and time course of fucose-containing glycoprotein synthesis and intracellular translocation in osteoclasts of the mice maxillary alveolar bone were investigated by electron microscopic radioautography. Male Balb-C mice weighing 17gm were anesthetized with Nembutal and injected via the external jugular vein with 2.5 mCi of $L-[6-^{3}H]-fucose$ (specific activity 16.8 mCi/mmol) in 0.1 ml of sterile saline solution. At 5, 10, 20, 35 minutes and 8 hours after administration of the $^{3}H-fucose$, animals were killed by intracardiac perfusion of 30ml of 2% glutaraldehyde in a modified Tyroid solution, pH 7.4. The maxillae were then removed and further fixed in Karnovsky fixative for an additional 3-4 hours. After rinsing in 0.1M cacodylate buffer for 10 minutes, the maxillae were demineralized for 2 weeks at $4^{\circ}C$ in ethylene diamine tetra acetate containing 2% glutaraldehyde. The first interdental areas were mesiodistally sectioned into slices of 1mm thickness and postfixed in osmium tetroxide. Tissues were then dehydrated and embedded in Poly Bed. To prepare electron microscopic radioautography, the dipping method of Kopriwa (1973) was employed. Thin sections were coated with a crystalline monolayer of ILford $L_4$ photographic emulsion. After exposure for 4 months at $4^{\circ}C$, the sections were developed Kodak Microdol-X and Phenidon (for compact grains), fixed in 30% sodium thiosulfate, stained with uranyl acetate and lead citrate and examined in the electron microscope (JEOL 1200 EX). At 5, 10 and 20 minutes after injection, $^{3}H-fucose$ was concentrated in Golgi cisternae of the osteoblasts. By 35 minutes the labels were observed over small vesicles in the suprannclear area of osteoclasts. At 8 hours, numerous silver grains were located on the ruffled border and cell membrane of osteoclasts. These results indicate that fucose molecules are added in the Golgi apparatus and small vesicles appear to be responsible for translocation of the glycoproteins to the marginal portion of osteoblasts. The glycoproteins are distributed on the osteoclast cell surface and especially over the ruffled border.

• 대한수의학회지
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• 제32권4호
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• pp.489-496
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• 1992

The division, distribution and migration of the macroglial cells in the juvenile mouse brain were investigated with the radioautography. Forty mice (ICR) were randomly subdivided into two groups. The twenty mice from group 1 were weighing initially 5 to 6g, aged 10 to 12 days and were sacrificied at 2 hrs, 2, 3, 5, 7, 10, 15 and 20 days after a single intraperitoneal injection of $^3H$-thymichine ($4{\mu}$ Ci/g of body weight). Twenty mice from group 2 were weighing intially 2.5 to 5g, aged 3 to 8 days and were sacrificed at 2 hrs, 2, 3, 5. 7, 10, 15 and 20 days after a single($4{\mu}$ Ci/g of body weight) and/or after intraperitoneal repeated injections($2{\mu}$ Ci/g of body weight/interval) at 2, 3 and 5 days after the first injection. The brain preparations were processed for autoradiogrouphy using Kodak NTB-3 emulsion following development in Kodak D-19, fixation in Kodak fixer, and then stained with cresyl echt violet or hematoxylin counterstain. The labeling index of the ectodermal glial cells in the subependymal layers of the lateral ventricles (SLLV), corpus callosum (CC), molecular layer of the neocortex (MLN ), inner layer except the molecular layer in the neocortex (ILN) and medulla of the cerebrum (MC) were invested. 1. Labeling cells appeared from 2 hour and some of them sustained in the 20 day after injection. In the single injection group, the peak of the labeling index reached a 7.6% at 3 day, 3.6% at 7 day, 3.3% at 2 day, 5.0% at 3 day and 2.3% at 2 day from the SLLV. CC, MLN, ILN and MC, respectively. In the repeated injecton group, the peak of the labeling index reached a 32.0 at 7 day, 11.0% at 10 day, 89% at 7 day, 16.0% at 10 day and 10.8% at 15 day from the SLLV, CC, MLN, ILM and MC, respectively. 2 The glial cells of the SLLV were recognized as to be migrated into the CC and to be not or less to be into the MC and ILN but to be not into the MLN. Glial cell aggregates in the neocotex and MC were recognized as to be proliferated and then disappeared in the itself regions.

• 치과방사선
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• 제17권1호
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• pp.51-87
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• 1987

The incorporation of ³H-proline by epithelial and connective tissue elements of rat palatal mucosae was studied in order to investigate the relative levels of protein synthesis by the epithelium and underlying connective tissue cells. Following a sixty minutes incorporation of the radioactive tracer in vitro, it was found that the suprabasal cells had most grains per unit area. Furthermore, the grains were more concentrated over the cytoplasm than the nucleus. This was in contrast with the labeling of basal cells which had twice as many grains over the nucleoplasm than that over the cytoplasm. In intermediate cells; i.e., the spinous layer, the number of silver grains per unit area was decreased from that of the suprabasal cells. In areas where desmosomes were more prominent, many grains were in touch with such desmosomes. However, the labeling appeared to be reduced as soon as the cells became flattened. Moreover, the epidermal keratohyalin granules were relatively free of grains. Except for certain intercellular surfaces the keratinized cells were generally free of grains. On the connective tissue side, silver grains were primarily localized over the fibroblasts with occasional grains being found over palatal muscle cells, neural elements and so on. Most grains over collagenous fibers were found in relation to mature collagen fibrils. Thus, protein synthesis in isolated mucosae of the rat palate appeared to take place both in epithelial and connective elements. There were no apparent tissue alterations caused by the in vitro incorporation procedure utilized under conditions of this study.

• 치과방사선
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• 제17권1호
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• pp.27-49
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• 1987

Using ³H-proline as a radioactive tracer, the relationship between the ultrastructural differentiation and the site of protein synthesis has been investigated in developing red blood corpuscles. The general ultra-structure of erythropoietic cells in differentiation after 60 minutes of in vitro labeling has confirmed the results from previous investigations by Bessis, M., Thiery, J. and others. In dividing nuclei more than two-thirds of the labeling were present at the interface between heterochromatin and euchromatin. In less differentiated cells most of the grains in interphase cells was localized over the nucleus. As the cells continued to develope beyond a stage where cytoplasmic density was clearly increased over other cell lines in bone marrow, the majority of grains localized over the cytoplasmic area was decreased in more mature cells, as judged by the density of cytoplasm, and the structural changes in mitochondria, Golgi complex and polysomal configurations. These results show; 1) that the cytoplasm of erythroblast series does not change under in vitro conditions employed in the study; 2) that protein synthesis in the nucleus occurs largely at the interface between euchromatin and heterochromatin in active nuclei; and 3) that cytoplasmic synthesis of proteins continues to take place well into the normoblast stage solong as the physically visible polysomes are present in maturing red blood corpuscles.

• Nuclear Engineering and Technology
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• 제12권2호
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• pp.81-87
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• 1980

락토퍼옥시데이즈(lactoperoxidase, LPO)를 사용하여 인슈린을 $^{125}$/I로 표지반응 시켰다. 반응생성물은 전분젤 전기영동(SGE) 과 세파덱스 젤여과(SF) 둥 두단계를 거쳐 정제하였다. 표지수율 과표지생성물의 항체에 대한 결합능으로 보아 종래의 클로라민-T법 (표지수율 약 35%)보다 효소법 (표지수율 약 50%)이 우수하였다. 인슈린의 첨가없이 LPO법으로 표지반응을 진행시킨 다음 SGE, 종이 크로마토그래피, 방사선사진술 등을 적용하여 LPO법에서의 부산물을 확인할 수 있었다. SGE와 SF에서의 분리 분별 부분에 관해서도 분석, 토의하였다.