Periodontal disease (PD) is strongly linked to increased risk of oral squamous cell carcinoma (OSCC); however, the specific mechanism through which the development of PD and OSCC is simultaneously promoted remains unclear. This study explored the impact of periodontal pathogens on OSCC progression and the contribution of periodontal pathogen-stimulated OSCC to PD development. The expression of osteoclastogenesis-inducing factors was assessed using quantitative reverse transcription polymerase chain reaction analysis following stimulation of OSCC with lipopolysaccharide (LPS) derived from the periodontal pathogen Porphyromonas gingivalis (Pg), a pathogen commonly responsible for PD. The cell counting kit-8 assay was used to determine the effects of Pg-LPS on OSCC proliferation and drug resistance to cisplatin and 5-fluorouracil. The effects of conditioned medium (CM) derived from Pg-LPS–stimulated OSCC on osteoclastogenesis was evaluated using tartrate-resistant acid phosphatase (TRAP) staining on bone marrow-derived macrophages (BMMs). Pg-LPS administration in SCC-25 and YD-8 OSCC cell lines induced a significant increase in receptor activator of nuclear factor kappa-B ligand mRNA expression; however, it did not affect cell proliferation. Treatment with CM derived from Pg-LPS–stimulated SCC-25 or YD-8 cells markedly enhanced the formation of TRAP-positive multinucleated cells during osteoclast differentiation of BMMs. Altogether, these findings demonstrate that Pg-LPS–stimulated OSCC promoted osteoclastogenesis through a paracrine mechanism.

기후 변화의 가속화로 국내 제주 및 남부 지방을 중심으로 열대 및 아열대 작물의 재배 및 소비가 증가하는 추세이다.오크라는 식용적 가치가 있을 뿐만 아니라, 품종별 고유의 꼬 투리와 잎의 색은 관상적 가치가 있어 조경 식물로 많이 사용 되고 있다. 본 연구는 도심 내 옥상 온실에 관상식물인 오크 라를 도입하기 위해 피트모스와 펄라이트 비율에 따른 기초 종자 발아 및 육묘기 실험을 진행하였다. 피트모스와 펄라이 트 비율은 PT:PL=1:2, 1:1, 2:1, 4:1 네 가지로 조성하였다. 발 아율은 파종 후 7일차부터 다른 처리구에 비해 피트모스:펄라 이트=1:2의 처리구에서 가장 높았다. 파종 후 28일차와 70일 차에 줄기길이, 경경, 뿌리길이, 지상부와 지하부의 생체중과 건물중 그리고 엽면적은 피트모스:펄라이트=1:2 처리구에서 가장 높았다. 그러나, 파종 후 56일 이후부터 엽수는 피트모 스:펄라이트=1:2, 2:1, 4:1 처리구에서 감소하였다. 피트모스: 펄라이트=1:1, 2:1, 4:1 처리구에서 식물이 필요로 하는 피트 모스의 비율이 지나치게 높아 높은 피트모스 비율로 인하여 수분함수량이 과도하게 높아 식물이 고사한 것으로 판단된다. 따라서 오크라를 관상식물로 활용하기 위해서는 피트모스와 펄라이트를 1:2로 혼합한 배지가 가장 적합하다.

Although the effect of elevated carbon dioxide (CO2) on Phalaenopsis plant flowering, biomass, and photosynthesis has received intensive study, whether elevated CO2 affects plant requirements and sensitivity to potassium sulfate (SOP) during the reproductive growth stage remains unclear. To evaluate the combined effect of CO2 and SOP provision on crassulacean acid metabolism orchids, we cultivated Phalaenopsis Queen Beer ‘Mantefon’ under ambient and elevated CO2 treatments (≈ 400 or ≈ 720 μmol×mol-1, respectively) and four levels of SOP supply for 20 weeks after treatments (WAT): potassium and sulfate levels by 10.41 and 1.96 mmol·L-1 (SOP1), 5.98 and 0.90 mmol·L-1 (SOP2), 12.80 and 1.96 mmol·L-1 (SOP3), and 14.83 and 3.16 mmol·L-1 (SOP4), respectively. The number of floral buds and flowers decreased in the plants grown under elevated CO2 than in those grown under ambient CO2, regardless of the SOP level; however, the reduced production of floral buds and flowers did not affect the dry mass of shoot, root, and spike at 20 WAT. There were significant interactive effects of CO2 and SOP on root biomass accumulation and net CO2 uptake. The stimulation of biomass partitioning on the root, as a sink source, observed due to the uptake of elevated CO2 was improved under increased SOP supply. Under ambient CO2, the leaf critical SOP level was SOP1 for root and spike biomass accumulation. Plants grown under elevated CO2 were more sensitive to SOP treatments, with higher essential leaf levels of SOP.

Cymbidium is one of the most popular and economically important species cultivated as a commercial ornamental crop. The objectives of this study were to determine the appropriate electrical conductivity (EC) treatments of nutrient solution, which gives the highest spike production and quality. Three-year-old Cymbidium ‘Lovely Smile’ plants were grown in the environmentally controlled Information and Communication Technology (ICT) smart greenhouse at Seoul Women’s University. The EC of the nutrient solution was changed in three distinct stages: vegetative, flower initiation, and flower development. The EC treatments were 1-0-1 (dS·m-1, EC101), 1-1-1 (dS·m-1, EC111), 2-1-2 (dS·m-1, EC212), 2-2-2 (dS·m-1, EC222), 3-2-3 (dS·m-1, EC323), 3-3-3 (dS·m-1, EC333) and the pH was adjusted to 6.0–6.5. Pseudobulb diameter increased in the plants treated with EC 101 and EC111 compared to the plants treated with EC 2.0–3.0 dS·m-1 at the reproductive stage 28 weeks after nutrient solution treatment. Flower spike production per pot and pseudobulb showed the highest values in the plants treated with EC111 of 3.3 and 1.4, respectively. Flower spikes length was the highest in the plants treated with EC 1.0 dS·m-1 and stem thickness, number of flowers, and fresh weight were the largest in the plants with EC 1.0 dS·m-1 among the EC treatments. Flower spikes had the worst quality (e.g., plant growth and flowering quality) in the plants treated with EC 3.0 dS·m-1 among the EC treatments. Floral bud and flower development took place 1–2 weeks earlier in the plants treated with EC 101, 111, and 212 than the other treatments. Flower diameter showed the highest values in the plants treated with EC 1.0 dS·m-1 among the EC treatments and flower color showed higher L* and b* values and lower a* values in the plants treated with EC 3.0 dS·m-1 compared to EC 1.0 and 2.0 dS･m-1. Nutrient solution of EC 1.0 dS·m-1 (EC111) can be recommended to improve flower spike quality and advanced flower development of Cymbidium.