• 자원리싸이클링
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• 제20권2호
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• pp.3-15
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• 2011

현재 CDM사업 등록은 대부분 에너지, 화학공정, 제조공정 분야에서 이루어지고 있다. 그러나, 무기질 자원재활용을 통한 CDM사업 등록은 그렇게 많지 않은 실정이다. 본 논문에서는 국내 무기질 폐기물의 재자원화를 통한 CDM사업 등록 가능성을 알아보기 위하여 국내외 CDM사업 현황 분석 및 적용사례를 조사하였다. 조사결과 CDM사업 등록 사례는 대량으로 활용할 수 있는 산업 중의 하나인 시멘트산업의 원료 대체화 분야에서 다수의 등록이 이루어진 것으로 조사되었다. 우리나라에서의 CDM사업 적용 전망은 산업의 규모, 무기질 자원 활용 산업 및 온실가스 배출량을 분석하고 대량으로 활용할 수 있을 정도로 지속적으로 발생되는 우기질 폐가물의 현황 등을 면밀히 검토해야 할 것으로 판단된다.

• Journal of Periodontal and Implant Science
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• 제47권2호
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• pp.116-131
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• 2017

Purpose: The entry of bacteria or harmful substances through the epithelial seal of human gingival keratinocytes (HGKs) in the junctional epithelium (JE) is blocked by specialized intercellular junctions such as E-cadherin junctions (ECJs). However, the influence of roughened substrates, which may occur due to apical migration of the JE, root planing, or peri-implantitis, on the development of the ECJs of HGKs remains largely unknown. Methods: HGKs were cultured on substrates with varying levels of roughness, which were prepared by rubbing hydrophobic polystyrene dishes with silicon carbide papers. The activity of c-Jun N-terminal kinase (JNK) was inhibited with SP600125 or by transfection with JNK short hairpin RNA. The development of intercellular junctions was analyzed using scanning electron microscopy or confocal laser scanning microscopy after immunohistochemical staining of the cells for E-cadherin. The expression level of phospho-JNK was assessed by immunoblotting. Results: HGKs developed tight intercellular junctions devoid of wide intercellular gaps on smooth substrates and on rough substrates with low-nanometer dimensions (average roughness $[Ra]=121.3{\pm}13.4nm$), although the ECJs of HGKs on rough substrates with low-nanometer dimensions developed later than those of HGKs on smooth substrates. In contrast, HGKs developed short intercellular junctions with wide intercellular gaps on rough substrates with mid- or high-nanometer dimensions ($Ra=505.3{\pm}115.3nm$, $867.0{\pm}168.6nm$). Notably, the stability of the ECJs was low on the rough substrates, as demonstrated by the rapid destruction of the cell junction following calcium depletion. Inhibition of JNK activity promoted ECJ development in HGKs. JNK was closely associated with cortical actin in the regulation of ECJs in HGKs. Conclusions: These results indicate that on rough substrates with nanometer dimensions, the ECJs of HGKs develop slowly or defectively, and that this effect can be reversed by inhibiting JNK.