scholarly journals Titanium Culture Vessel Capable of Controlling Culture Temperature for Evaluation of Cell Thermotolerance

2021 ◽  
Vol 70 (6) ◽  
pp. 479-485
Author(s):  
Chikahiro IMASHIRO ◽  
Yuta IDA ◽  
Shogo MIYATA ◽  
Jun KOMOTORI
Keyword(s):  
Culture Vessel ◽  
Culture Temperature

scholarly journals Development of accurate temperature regulation culture system with metallic culture vessel demonstrates different thermal cytotoxicity in cancer and normal cells

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Chikahiro Imashiro ◽  
Haruka Takeshita ◽  
Takashi Morikura ◽  
Shogo Miyata ◽  
Kenjiro Takemura ◽  
...  
Keyword(s):  
Mrna Expression ◽  
Cancer Cells ◽  
Culture System ◽  
Dermal Fibroblasts ◽  
Culture Vessel ◽  
Thermal Stimulus ◽  
Culture Temperature ◽  
Hyperthermia Treatment ◽  
Normal Cells ◽  
C 30

AbstractHyperthermia has been studied as a noninvasive cancer treatment. Cancer cells show stronger thermal cytotoxicity than normal cells, which is exploited in hyperthermia. However, the absence of methods evaluating the thermal cytotoxicity in cells prevents the development of hyperthermia. To investigate the thermal cytotoxicity, culture temperature should be regulated. We, thus, developed a culture system regulating culture temperature immediately and accurately by employing metallic culture vessels. Michigan Cancer Foundation-7 cells and normal human dermal fibroblasts were used for models of cancer and normal cells. The findings showed cancer cells showed stronger thermal cytotoxicity than normal cells, which is quantitatively different from previous reports. This difference might be due to regulated culture temperature. The thermal stimulus condition (43 °C/30 min) was, further, focused for assays. The mRNA expression involving apoptosis changed dramatically in cancer cells, indicating the strong apoptotic trend. In contrast, the mRNA expression of heat shock protein (HSP) of normal cells upon the thermal stimulus was stronger than cancer cells. Furthermore, exclusively in normal cells, HSP localization to nucleus was confirmed. These movement of HSP confer thermotolerance to cells, which is consistent with the different thermal cytotoxicity between cancer and normal cells. In summary, our developed system can be used to develop hyperthermia treatment.

Cereal Callus Cultures: Control of Headspace Gases Can Optimise the Conditions for Callus Proliferation

1992 ◽  
Vol 40 (6) ◽  
pp. 737 ◽  
Author(s):  
SW Adkins
Keyword(s):  
Oryza Sativa L ◽  
Petri Dish ◽  
Triticum Aestivum L ◽  
Callus Cultures ◽  
Gaseous Atmosphere ◽  
Callus Growth ◽  
Culture Vessel ◽  
Rice Callus ◽  
Incubation Temperatures ◽  
Wheat Callus

The protective conditions under which callus cultures are grown to prevent microbial contamination and to reduce tissue desiccation cause the accumulation of volatiles in the vessel headspace and reduce the availability of oxygen for respiration. To demonstrate the importance of the gaseous atmosphere to culture growth a study was undertaken on non-morphogenic rice and wheat callus incubated under a number of environmental conditions. Changes in the gaseous atmosphere above rice (Oryza sativa L.) callus during routine culture in a petri dish suppressed growth and promoted necrosis. Incubating callus under a continuous flow of gas mixtures of known composition suggested that the inhibition of growth was caused by the accumulation of high levels of ethylene and to the rapid depletion of oxygen. In order to evaluate the importance of ethylene accumulation aminoethoxyvinyl glycine (AVG), I-aminocyclopropane-I-carboxylic acid (ACC) and silver nitrate (AgNO3) were added to the nutrient medium and ethylene was measured during callus culture. Ethylene restricted callus growth particularly under high (35°C) compared with moderate (25°C) incubation temperatures and under illuminated compared with dark incubation. Under illuminated incubation at 25°C, AVG ( 5 μM ) and AgNO3 (50 μM) improved rice callus growth by 69 and 54% respectively while ACC (100 μM) decreased growth by 15%. Furthermore, rice callus growth was better in large compared with small culture vessels since ethylene accumulation was reduced. In contrast, wheat (Triticum aestivum L.) callus grew well in the petri dish system and released very little ethylene into the culture vessel headspace. Growth was better under illuminated than darkened conditions and under moderate (25°C) compared with high (35°C) incubation temperatures. Furthermore, wheat callus growth was only marginally better in large compared with small culture vessels. Ethylene was not a restrictive factor of wheat callus growth since only low levels were detected in all conditions of incubation. Better control of ethylene and increased oxygen availability could be a way of increasing cell and tissue production for genetic engineering studies of otherwise recalcitrant species such as rice, and may be a way of improving manipulation of wheat.

A New Technology for Three-Dimensional Cell Culture: The Hydrodynamic Focusing Bioreactor

1999 ◽  
Author(s):  
Yow-Min D. Tsao ◽  
Steve R. Gonda
Keyword(s):  
Cell Culture ◽  
New Technology ◽  
Three Dimensional ◽  
Culture Vessel ◽  
Air Bubbles ◽  
Hydrodynamic Focusing ◽  
Shaped Cell ◽  
Fluid Environment ◽  
Dimensional Cell ◽  
Low Shear

Abstract The Hydrodynamic Focusing Bioreactor (HDFB) developed by NASA at the Johnson Space Center provides a unique hydrofocusing capability that simultaneously enables a low-shear culture environment and a unique hydrofocusing-based “herding” of suspended cells, cell aggregates, and air bubbles. The HDFB is a rotating dome-shaped cell culture vessel with a centrally located sampling port and an internal rotating viscous spinner attached to a rotating base. The vessel and viscous spinner can rotate at different speeds and in either the same or different directions. Adjusting the differential rotation rate between the vessel and spinner results in a controllable hydrodynamic focusing force. The resultant hydrodynamic force suspends the cells in a low-shear fluid environment that supports the formation of delicate three-dimensional tissue assemblies. Both suspension and anchorage-dependent cells have been successfully cultured.

Microwave Irradiation of PC3 Cells at Constant Culture Temperature Alters the Incorporation of BODIPY into Cells and Reduction of MTT

2017 ◽  
Vol 2 (26) ◽  
pp. 7983-7986 ◽  
Author(s):  
Sina Atrin Mazinani ◽  
Fereshteh Moradi ◽  
Jeffrey A. Stuart ◽  
Hongbin Yan
Keyword(s):  
Microwave Irradiation ◽  
Culture Temperature ◽  
Pc3 Cells

scholarly journals Pengaruh jenis penutup botol kultur terhadap pertumbuhan planlet kelapa sawit (Elaeis guineensis Jacq.) Effect of different culture vessel closures on the growth of oil palm (Elaeis guineensis Jacq.) plantlets

2016 ◽  
Vol 79 (1) ◽  
Author(s):  
Masna Maya SINTA ◽  
Imron RIYADI ◽  
. UMARYONO
Keyword(s):  
Light Intensity ◽  
Oil Palm ◽  
Room Temperature ◽  
Elaeis Guineensis ◽  
Aluminum Foil ◽  
Culture Vessel ◽  
Shoot Height ◽  
Plantlet Growth ◽  
Vessel Closure ◽  
Elaeis Guineensis Jacq

AbstractMicroenvironment inside the culture vessel such astemperature, light intensity, relative humidity, and aerationaffect growth and development of plantlets. This experimentwas conducted to determine the effect of different culturevessel closures on microenvironmental conditions inside thevessel and on growth of plantlets of oil palm. Shoots of oilpalm derived from somatic embryos were cultured on DFmedium for eight weeks in transparent culture bottlescovered with five different vessel closures e.i. screw cap withplastic wrap, screw cap, plastic wrap, aluminum foil, andautoclavable plastic. The culture vessels were placed in theculture room with light intensity 20 µmol/m 2 /sec for 12 hoursphotoperiod, at room temperature 26°C. Parametersobserved on plantlet growth were shoot height, biomass freshweight, leaf number, and leaf color grade, while onmicroenvironment were temperature and light intensity. Atthe end of experiment, the volume and fresh weight of theremaining medium were measured to determine evaporationrate of each treatment. Results show that the use of differentculture vessel closures affected the microenvironment insidethe vessel, the volume of the remaining medium, and thegrowth of the plantlets. The closure increased thetemperature by 1.6 – 2.6°C and decreased the light intensityby 1.7 – 8.7 µmol/m 2 /sec inside the culture vessels dependson the culture vessel closures. Culture vessels with aluminumfoil closure had the lowest temperature (28.9°C) and thelowest light intensity (10.8 µmol/m 2 /sec) gave the best resultin the growth of the plantlets. Better plantlets growth wasalso observed in the culture vessel with autoclavable plasticclosure that less expensive, therefore it can be used as analternative vessel closure for the growth of oil palm plantlets.AbstrakLingkungan mikro di dalam botol kultur seperti suhu,intensitas cahaya, kelembaban nisbi dan aerasi mem-pengaruhi pertumbuhan dan perkembangan planlet.Penelitian ini dilakukan untuk mengetahui pengaruhpenggunaan penutup botol kultur yang berbeda terhadapkondisi lingkungan mikro di dalam botol kultur danpertumbuhan planlet kelapa sawit. Planlet kelapa sawit asalembrio somatik dikulturkan dalam botol kultur bening berisimedium DF selama delapan minggu dan ditutup mengguna-kan lima jenis penutup botol yang berbeda yaitu tutup ulirdengan plastik wrap, tutup ulir, plastik wrap, aluminium foildan plastik tahan diautoklaf. Kultur diletakkan dalam ruangkultur, di bawah lampu TL dengan intensitas cahaya20 µmol/m 2 /detik dan suhu ruang 26 o C. Parameterpertumbuhan planlet yang diamati adalah tinggi planlet,bobot basah, jumlah daun dan kelas warna daun, sedangkanlingkungan mikro adalah suhu dan intensitas cahaya. Padaakhir eksperimen, volume dan bobot basah medium yangtersisa diukur untuk mengetahui tingkat penguapan padasetiap perlakuan. Hasil penelitian menunjukkan bahwapenggunaan penutup botol yang berbeda berpengaruhterhadap lingkungan mikro, volume medium tersisa dalambotol kultur dan pertumbuhan planlet. Penutup botolmeningkatkan suhu 1,6 – 2,6 o C dan menurunkan intensitascahaya 1,7 – 8,7 µmol/m 2 /detik di dalam botol tergantungpada jenis penutup botol yang digunakan. Botol kulturdengan penutup berbahan aluminium foil mempunyaiintensitas cahaya terendah (10,8 µmol/m 2 /detik) dan suhuterendah (28,9 o C) memberikan hasil terbaik pada pembesaranplanlet kelapa sawit. Pertumbuhan planlet yang baik jugaterdapat pada botol kultur dengan penutup plastik tahandiautoklaf yang lebih murah, sehingga penutup ini dapatdigunakan sebagai pilihan untuk pembesaran planlet kelapasawit.

scholarly journals Pengaruh jenis penutup botol kultur terhadap pertumbuhan planlet kelapa sawit (Elaeis guineensis Jacq.) Effect of different culture vessel closures on the growth of oil palm (Elaeis guineensis Jacq.) plantlets

2016 ◽  
Vol 79 (1) ◽  
Author(s):  
Masna Maya SINTA ◽  
Imron RIYADI ◽  
. UMARYONO
Keyword(s):  
Light Intensity ◽  
Oil Palm ◽  
Room Temperature ◽  
Elaeis Guineensis ◽  
Aluminum Foil ◽  
Culture Vessel ◽  
Shoot Height ◽  
Plantlet Growth ◽  
Vessel Closure ◽  
Elaeis Guineensis Jacq

AbstractMicroenvironment inside the culture vessel such astemperature, light intensity, relative humidity, and aerationaffect growth and development of plantlets. This experimentwas conducted to determine the effect of different culturevessel closures on microenvironmental conditions inside thevessel and on growth of plantlets of oil palm. Shoots of oilpalm derived from somatic embryos were cultured on DFmedium for eight weeks in transparent culture bottlescovered with five different vessel closures e.i. screw cap withplastic wrap, screw cap, plastic wrap, aluminum foil, andautoclavable plastic. The culture vessels were placed in theculture room with light intensity 20 µmol/m 2 /sec for 12 hoursphotoperiod, at room temperature 26°C. Parametersobserved on plantlet growth were shoot height, biomass freshweight, leaf number, and leaf color grade, while onmicroenvironment were temperature and light intensity. Atthe end of experiment, the volume and fresh weight of theremaining medium were measured to determine evaporationrate of each treatment. Results show that the use of differentculture vessel closures affected the microenvironment insidethe vessel, the volume of the remaining medium, and thegrowth of the plantlets. The closure increased thetemperature by 1.6 – 2.6°C and decreased the light intensityby 1.7 – 8.7 µmol/m 2 /sec inside the culture vessels dependson the culture vessel closures. Culture vessels with aluminumfoil closure had the lowest temperature (28.9°C) and thelowest light intensity (10.8 µmol/m 2 /sec) gave the best resultin the growth of the plantlets. Better plantlets growth wasalso observed in the culture vessel with autoclavable plasticclosure that less expensive, therefore it can be used as analternative vessel closure for the growth of oil palm plantlets.AbstrakLingkungan mikro di dalam botol kultur seperti suhu,intensitas cahaya, kelembaban nisbi dan aerasi mem-pengaruhi pertumbuhan dan perkembangan planlet.Penelitian ini dilakukan untuk mengetahui pengaruhpenggunaan penutup botol kultur yang berbeda terhadapkondisi lingkungan mikro di dalam botol kultur danpertumbuhan planlet kelapa sawit. Planlet kelapa sawit asalembrio somatik dikulturkan dalam botol kultur bening berisimedium DF selama delapan minggu dan ditutup mengguna-kan lima jenis penutup botol yang berbeda yaitu tutup ulirdengan plastik wrap, tutup ulir, plastik wrap, aluminium foildan plastik tahan diautoklaf. Kultur diletakkan dalam ruangkultur, di bawah lampu TL dengan intensitas cahaya20 µmol/m 2 /detik dan suhu ruang 26 o C. Parameterpertumbuhan planlet yang diamati adalah tinggi planlet,bobot basah, jumlah daun dan kelas warna daun, sedangkanlingkungan mikro adalah suhu dan intensitas cahaya. Padaakhir eksperimen, volume dan bobot basah medium yangtersisa diukur untuk mengetahui tingkat penguapan padasetiap perlakuan. Hasil penelitian menunjukkan bahwapenggunaan penutup botol yang berbeda berpengaruhterhadap lingkungan mikro, volume medium tersisa dalambotol kultur dan pertumbuhan planlet. Penutup botolmeningkatkan suhu 1,6 – 2,6 o C dan menurunkan intensitascahaya 1,7 – 8,7 µmol/m 2 /detik di dalam botol tergantungpada jenis penutup botol yang digunakan. Botol kulturdengan penutup berbahan aluminium foil mempunyaiintensitas cahaya terendah (10,8 µmol/m 2 /detik) dan suhuterendah (28,9 o C) memberikan hasil terbaik pada pembesaranplanlet kelapa sawit. Pertumbuhan planlet yang baik jugaterdapat pada botol kultur dengan penutup plastik tahandiautoklaf yang lebih murah, sehingga penutup ini dapatdigunakan sebagai pilihan untuk pembesaran planlet kelapasawit.

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