• Animal cells and systems
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• 제2권4호
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• pp.501-506
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• 1998

In the goby Micropercops swinhonis, the development of its egg's enveloping layers could be divided into 4 stages. In the earliest developmental period, stage I, there is a simple oocyte surrounded by a layer of squamous follicular cells. Stage II corresponds to the yolk vesicle stage of vitellogenesis. Here the initial follicular layer has become bilaminar with the retention of its outer squamous cell layer and the acquisition of an inner cuboidal cell layer just over the zona radiata. The number and size of the cuboidal cells increases throughout this stage. Stage III corresponds to the yolk granule stage of true vitellogenesis. Here the cuboidal cells begin to be replaced by columnar cells. As the oocyte grows, the columnar cells increase in size. The columnar cells produce cytoplasmic neutral mucins and by the end of this stage their cytoplasm has been filled with this mucin. In stage IV a single layer of squamous cells still remained as the outer follicular layer of the oocyte. The secretory activity of the inner follicular layers' columnar cells has ceased and they had lost their cell wall integrity and ended as a series of bullet-shaped, neutral mucin deposits.

• Natural Product Sciences
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• 제13권4호
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• pp.283-288
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• 2007

Acanthopanacis Cortex (AC) has been popularly used as an herbal medicine for medical treatment of rheumatoid arthritis, insomnia, impotence and diabetes. Here, we investigated immunostimulating effects of the aqueous extract of AC on macrophage. We studied nitric oxide (NO) and tumor necrosis factor (TNF)-${\alpha}$ release in response to AC treatment, as they are important secretory products of macrophage. AC alone induce the NO and TNF-${\alpha}$ production. AC increase c-Jun NH2-terminal kinase 1/2 (JNK) and extracellular signal-regulated kinase (ERK) phosphorylation but does not p38 activation in RAW 264.7 cells. Also AC resulted in the enhanced cell-surface expression of CD80 and CD14. In addition, AC resulted in enhanced T cell-stimulatory capacity and increased T cell secretion of interferon (IFN)-gamma. After feeding with AC to mouse for 10 days, the change of $CD28^+$ and $CD40^+$ population was analyzed. AC increased $CD28^+$ population in splenocytes in vivo. These studies indicate that AC induces macrophage activation and suggest the possible use of AC in macrophage-based immunotherapies.

• Parasites, Hosts and Diseases
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• 제31권4호
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• pp.315-320
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• 1993

Fibricola seoulensis 조직융해구(tribocytic organ)의 미세구조를 알기 위하여, 전자현미경으로 관찰하였다. 조직응해구의 표피에서 미세응모가 관찰되었다. 조직융해구에는 3가지 형태의 세포들이 관찰되는 데, 첫째는 방추형이고, 핵 및 원형질이 전자밀도가 낮고, 원형질내 직경 $0.1-0.2{\;}\mu\textrm{m}$의 과립이 소수 관찰된다 둘째는 방추형이고, 핵 및 원형질이 전자밀도가 높고, 직경 $0.1-0.2{\;}\mu\textrm{m}$의 미립자로 구성된 과립을 포함한다 셋째는 원형질이 전자밀도가 높고, 직경 $0.3-1.2{\;}\mu\textrm{m}$의 과립을 다수 포함한다. 위의 세포들 중, 첫째와 둘째 세포는 표피세포로, 셋째는 조직응해구의 특 이 분비세포로 추정한다. 이것은 조직융해구의 분비 기능을 설명할 수 있는 또 다른 소견이라고 할 수 있다.

• 한국작물학회:학술대회논문집
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• 한국작물학회 2007년도 춘계학술발표회
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• pp.65-73
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• 2007

The objective of this study is to understand how regulatory mechanisms respond to sugar status for more efficient carbon utilization and source-sink regulation in plants. So, we need to identify and characterize many components of sugar-response pathways for a better understanding of sugar responses. For this end, genes responding change of sugar status were screened using Arabidpsis cDNA arrays, and confirmed thirty-six genes to be regulated by sucrose supply in detached leaves by RNA blot analysis. Eleven of them encoding proteins for amino acid metabolism and carbohydrate metabolism were repressed by sugars. The remaining genes induced by sugar supply were for protein synthesis including ribosomal proteins and elongation factors. Among them, I focused on three hydrolase genes encoding putative $\beta$-galactosidase, $\beta$-xylosidase, and $\beta$-glucosidase that were transcriptionally induced in sugar starvation. Homology search indicated that these enzymes were involved in hydrolysis of cell wall polysaccharides. In addition to my results, recent transcriptome analysis suggested multiple genes for cell wall degradation were induced by sugar starvation. Thus, I hypothesized that enzyme for cell wall degradation were synthesized and secreted to hydrolyze cell wall polysaccharides producing carbon source under sugar-starved conditions. In fact, the enzymatic activities of these three enzymes increased in culture medium of Arabidopsis suspension cells under sugar starvation. The $\beta$-galactosidase encoded by At5g56870 was identified as a secretory protein in culture medium of suspension cells by mass spectrometry analysis. This protein was specifically detected under sugar-starved condition with a specific antibody. Induction of these genes was repressed in suspension cells grown with galactose, xylose and glucose as well as with sucrose. In planta, expression of the genes and protein accumulation were detected when photosynthesis was inhibited. Glycosyl hydrolase activity against galactan also increased during sugar starvation. Further, contents of cell wall polysaccharides especially pectin and hemicellulose were markedly decreased associating with sugar starvation in detached leaves. The amount of monosaccharide in pectin and hemicellulose in detached leaves decreased in response to sugar starvation. These results supported my idea that cell wall has one of function to supply carbon source in addition to determination of cell shape and physical support of plant bodies.

• 한국균학회지
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• 제35권1호
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• pp.1-10
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• 2007

세포벽은 진균류의 생존과 삼투안전성 유지에 필수적인 구조체로, 세포부착성 단백질이나 가수분해효소 등과 같은 생물학적 활성을 갖는 다양한 단백질이 결합하거나 그 속에 자리잡고 작용할 수 있게 한다. 최근 효모류인 Saccharomyces cerevisiae와 사상균인 Aspergillus nidulans에서 세포 내 단백질 분비 소낭의 하나인 COPI 소낭을 구성하는 ${\alpha}-COP$ 단백질에 돌연변이가 일어날 경우, 온도의존적 삼투감수성이 나타나는 것으로 밝혀졌다. 이러한 사실은 ${\alpha}-COP$이 베타-1,3-글루칸 합성효소 복합체를 구성하는 단백질과 세포벽 단백질의 이송과정에 중요한 역할을 함으로써 세포벽 안정성 유지에 기여함을 시사하는 것이다. 본 총설에서는 세포 내 단백질 이송기구 중에서도 COPI 소낭을 구성하는 ${\alpha}-COP$과 균류의 세포벽 형성과정과의 관계에 대하여 기술하는 한편, 단백질 분비기구에 결손이 생긴 돌연변 이주를 이용한 세포벽 합성기작에 대한 기초 및 응용연구의 가능성에 대하여 검토하여 보았다.

• Applied Microscopy
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• 제22권1호
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• pp.1-14
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• 1992

Parenchyma of the cat pineal body consisted of pinealocytes and glial cells. The pinealocyte, predominant cell type, was characterized by having large mitochondria with pale matrix, abundant polyribosomes, moderately-developed Golgi apparatus, centrioles and occasional cilia. The pinealocyte had one thick and long cytoplasmic process at the one pole of the cell, and slender and shorter processes at the other pole, and in addition occasional short processes from the cell body. These processes contained longitudinally arranged microtubules, and a few mitochondria. Thick processes teminated as bulgings either in the intercellular process-rich area, or in the perivascular border which was formed by glial cell processes. These endings of pinealocyte processes had many small vesicles, mitochondria, and occasional dense bodies. Glial cells with abundant filaments of intermediate type and clear cytoplasmic matrix were fibrous astrocyte. Perikarya of the astrocytes had small and dense mitochondria, moderately developed Golgi apparatus, dense bodies and variable amount of intermediate filaments. Glial cell processes run through the intercellular spaces among the pinealocyte processes. Glial cell of protoplasmic type had no or a few filaments, but it had well-organized rough endoplasmic reticulum, dense mitochondria, well developed Golgi apparatus and many dense granules. Intercellular canaliculi formed by adjacent pinealocytes and glial cell processes were often noted. Within the parenchyma, sympathetic and parasympathetic axons and their endings were noted. These endings were present mostly in the intercellular spaces without having membrane specialization, however, in rare instances, ending with small clear and dense cored vesicles, and large dense cored vesicles formed specialized synapse with a pinealocyte process. Within the perivascular spaces nerve fibers and endings, Schwann cells and pericyte were noted. In rare case pinealocyte process penetrated into the perivascular space through the interuptions of glial border. These results suggest that pinealocyte of the cat has less significance in secretory function and is rather neural type of cell.

• 한국패류학회지
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• 제24권1호
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• pp.41-50
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• 2008

소라 (Batillus cornutus) 외투막의 조직화학적 특성 및 미세구조를 광학현미경과 투과전자현미경을 이용하여 기재하였다. 소라의 외투막은 결합조직층을 단층상 피층이 위아래로 둘러싸고 있는 구조였으며, 상피층은 내장 기관계 쪽을 향하고 있는 내부상피층과 패각 쪽의 외부상피층으로 구분된다. 상피층에 의해 둘러싸인 결합조직층은 주로 교원섬유와 근섬유다발로 구성되며, 혈림프동이 발달하고 있었다. 외투막의 각정부 상피층에 분포하는 점액세포들은 산성 및 중성 점액다당류를 함유하고 있었으며, 중간부와 가장자리의 상피층에 분포하는 점액세포들은 비황화 강산성의 당단백질 점액성분을 함유하는 것으로 나타났다. 외투막의 두께, 상피층의 두께, 혈림프동의 면적은 각정부에서 가장자리로 갈수록 낮아지는 경향을 보였다. 투과전자현미경으로 관찰하였을 때 외투막의 상피층은 단층으로 원주형 상피세포, 섬모세포, 흡수세포, 분비세포로 구성되어 있었다. 외투막 상피세포들은 원주형으로 장방형의 핵을 가지며, 자유면에는 미세융모들이 발달되어 있었다. 상피세포 사이에는 폐쇄띠, 폐쇄대와 수지상막구조로 연결되어 있었다. 섬모세포는 자유면에 섬모와 미세융모를 가지며, 세포질의 상부에는 다수의 미토콘드리아를 가지고 있었다. 상피층에서는 흡수기능을 가지는 두 종류의 세포가 관찰되었다. 이들은 원주형으로 미세융모, 음소포, 미토콘드리아 그리고 전자밀도가 다양한 용해소체들을 함유하고 있었다. 소라 외투막에서는 네 종류 (A, B, C, D)의 분비세포를 구분할 수 있었는데, 이들은 모두 단세포선으로 확인되어 대부분의 복족류와 이매패류의 외투막에서 보고된 선세포들과 유사한 특징을 보였다.

• 대한화장품학회:학술대회논문집
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• 대한화장품학회 2003년도 IFSCC Conference Proceeding Book II
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• pp.508-518
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• 2003

SZ95 cell is an immortalized human sebaceous gland cell line that shows the morphologic, phenotypic and functional characteristics of normal human sebocytes. Sebocytes may play crucial parts in the pathophysiologic processes and disorders of the pilosebaceous unit. The secretory activity of the sebaceous gland is remarkably species-specific and acne is an exclusively human disease. Thus, this SZ95 cells offer possibilities for investigations on the physiology of the sebaceous gland and its role in sebum-associated skin disease such as acne. In this study, we investigated the effects of 13-cis-retinoic acid (13-cis-RA) and spironolactone, frequently used as therapeutic agents of acne, on the lipid synthesis and proliferation of human sebocytes. Cell proliferation was determined by MTT assay and cytoplasmic lipid droplets was shown by Oil-red a staining. Total lipid levels were biochemically estimated by the sulfo-phospho-vanilline reagent. 13-cis-RA and spironolactone significantly inhibited proliferation and lipid levels in a dose-dependent manner. Combined treatment with testosterone and 13-cis-RA or spironolactone resulted in a lower total lipid levels than that with androgen alone. These observations indicate that 13-cis-RA and spironolactone are potent inhibitors of both cell proliferation and lipid synthesis in human sebocytes. We will provide experimental evidence that this human sebocyte cell line serves as an adequate tool for evaluating the anti-lipogenic activity of various compounds potentially useful for the bioactive cosmeceutical ingredients on acne skin, and studying the intracellular biochemical markers depending on the types of compounds from various sources.

• Molecules and Cells
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• 제44권10호
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• pp.723-735
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• 2021

Spemann organizer is a center of dorsal mesoderm and itself retains the mesoderm character, but it has a stimulatory role for neighboring ectoderm cells in becoming neuroectoderm in gastrula embryos. Goosecoid (Gsc) overexpression in ventral region promotes secondary axis formation including neural tissues, but the role of gsc in neural specification could be indirect. We examined the neural inhibitory and stimulatory roles of gsc in the same cell and neighboring cells contexts. In the animal cap explant system, Gsc overexpression inhibited expression of neural specific genes including foxd4l1.1, zic3, ncam, and neurod. Genome-wide chromatin immunoprecipitation sequencing (ChIP-seq) and promoter analysis of early neural genes of foxd4l1.1 and zic3 were performed to show that the neural inhibitory mode of gsc was direct. Site-directed mutagenesis and serially deleted construct studies of foxd4l1.1 promoter revealed that Gsc directly binds within the foxd4l1.1 promoter to repress its expression. Conjugation assay of animal cap explants was also performed to demonstrate an indirect neural stimulatory role for gsc. The genes for secretory molecules, Chordin and Noggin, were up-regulated in gsc injected cells with the neural fate only achieved in gsc uninjected neighboring cells. These experiments suggested that gsc regulates neuroectoderm formation negatively when expressed in the same cell and positively in neighboring cells via soluble factors. One is a direct suppressive circuit of neural genes in gsc expressing mesoderm cells and the other is an indirect stimulatory circuit for neurogenesis in neighboring ectoderm cells via secreted BMP antagonizers.

• Applied Microscopy
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• 제28권3호
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• pp.345-362
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• 1998

In order to the comparative morphological study of the non-ciliated and ciliated epithelial cells, and to elucidate the process of degeneration of non-ciliated epithelial cell of the ductus epididymidis, Korean striped field mouse, Apodemus agrarius coreae was examined with light and transmission electron microscopes. The morphological characteristics of non-ciliated epithelial cell, the cell types of the caput epididymidis (Cp), corpus epididymidis (Cr) and cauda epididymidis (Cu) were long-columnar, short-columnar and short-cuboudal, respectively. The mitochondria and rough endoplasmic reticulum tended to be broken as they immigrated from Cp to the Cu. The Golgi acted vigorously at the Cp, but the Golgi was inactive in Cr and Cu. The secretory vesicles and lysosomes were increased gradually from Cp to the Cu. The process of degeneration of the non-ciliated epithelial cells observed in the Cp, Cr and Cu epididymidis. The increase of the non-ciliated epithelial cells, and its degeneration were observed more often from Cp to the Cu. The morphological characteristics of the ciliated epithelial cells, the cell types of the Cp, Cr and Cu were long-columnar, short-columnar and short-cuboudal, respecptively like the non-ciliated epithelial cells. The stereocilia was long and slender at the Cp and Cr, while Cu was very short. The pinocytotic vesicles and absorptive vesicles were increased from the Cp to the Cu. Numerous disintergrated products was existed at the Cr including the Cp, but Cu were not observed. A significant amount of lysosomes existed at the Cp and Cr epithelial cells, but they were not observed in Cu epithelial cells.