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Human thp 1 cells

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The Human THP-1 cells are a monocytic cell line derived from the peripheral blood of a 1-year-old male with acute monocytic leukemia. These cells are commonly used in research to study monocyte and macrophage biology, inflammation, and immune response.

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16 protocols using human thp 1 cells

1

Culturing Pancreatic and Immune Cells

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Human PANC-1 and MIA PaCa2 pancreatic cancer cells (ATCC, Manassas, VA) were cultured in DMEM (Gibco, Thermo Fischer Scientific, Waltham, MA) with 4.5 g/mL glucose, and human THP-1 cells (ATCC) were cultured in RPMI-1640 (Gibco). All cell culture media were supplemented with 10% fetal bovine serum (FBS), L-glutamine (2 mM), except RPMI-1640 media for conditioned media experiments, which was supplemented with 1X GlutaMAX (Gibco), penicillin (100 units/mL) (Gibco), and streptomycin (500 μg/mL) (Lonza, Basel, Switzerland) in regular cell culture procedures. Cultures were incubated in 5% CO2 incubators at 37 °C. All cell lines were authenticated by STR profiling (Promega PowerPlex, Leiden, Netherlands) and tested for mycoplasma by PCR monthly.
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2

Culturing Diverse Microbial and Mammalian Cells

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M. luteus (ATCC 4698) and S. aureus (ATCC 25923) were cultured in tryptic soy broth. GFP-E. coli was generated as described32 (link) and cultured in LB medium. Drosophila S2 cells (RRID: CVCL_TZ72) and S2R+ cells (RRID: CVCL_Z831) were cultured at 25 °C in Drosophila Schneider’s Medium (Biological Industries) supplemented with 10% FBS and antibiotics. Human HEK293T cells (ATCC#CRL-11268) and mouse MEF cells (ATCC#CRL-2991) were cultured at 37 °C in DMEM medium (Sigma) supplemented with 10% FBS and antibiotics. Human THP-1 cells (ATCC#TIB-202) were cultured at 37 °C in RPMI 1640 medium (Sigma) supplemented with 10% FBS and antibiotics.
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3

Molecular Cloning of YAP, p65, IKKα/β

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The 293T and MCF7 cell lines were maintained in high-glucose Dulbecco’s modified Eagle’s medium (Invitrogen, Waltham, MA, USA) supplemented with 10% fetal bovin serum (Gibco, Grand Island, NY, USA), 50 U/ml penicillin, 50 μg/ml streptomycin, in 5% CO2 atmosphere at 37 °C. Human THP-1 cells (from ATCC, Manassas, VA, USA) were cultured in RPMI-1640 medium with 10% fetal calf serum, 50 U/ml penicillin and 50 μg/ml streptomycin. Macrophages were prepared from THP-1 cells using 100 ng/ml PMA (Sigma-Aldrich, St Louis, MO, USA) treatment for 3 days.
Complementary DNA of YAP was subcloned into pQCXIH and pEGFP-C2 expression vector. Myc-p65 complementary DNA was subcloned into pQCXIH expression vector. Flag-IKKα and HA-IKKβ/ε were gifts from Dr Hongbin Shu.
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4

Bead-based Phagocytosis Assay for BDBV

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Recombinant BDBV GP was biotinylated and conjugated to streptavidin-coated Alexa488 beads (Life Technologies). BDBV-coated beads were incubated with antibodies at 5 μg/ml in culture medium for 2 hours at 37°C. Human THP-1 cells (ATCC) were added at a concentration of 2.5 x 104 cells/well and incubated for 18 hours at 37°C in 96-well plates. Cells were fixed with 4% paraformaldehyde and analyzed by flow cytometry on a BD LSRII using Diva software and FlowJo analysis software. The phagocytic score was determined using the following calculation: (% of AlexaFluor488+ cells)*(AlexaFluor488 geometric MFI of AlexaFluor488+ cells)/10,000.
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5

Isolation and Culture of Macrophages

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NHBE cells were purchased from Lonza (Walkersville, MD, USA), and cultured in collagen-coated plates in LHC-9 medium (Life Technologies, Grand Island, NY, USA). Human THP-1 cells (American Type Culture Collection, Manassas, VA, USA) were cultured for 3 days with 200 nM phorbol 12-myristate 13-acetate to induce macrophage differentiation (16 (link)). Human alveolar macrophages were isolated by centrifugation of bronchoalveolar lavage fluid from healthy adult volunteers using a protocol approved by the University of Arizona College of Medicine Institutional Review Board. Bone marrow cells were harvested from the femurs and tibias of C57BL6/J mice, and peritoneal macrophages were isolated from thioglycolate-treated C57BL6/J mice as described (17 ) using a protocol approved by the University of Arizona Collage of Medicine Institutional Animal Care and Use Committee. Bone marrow cells were cultured for 7 days with 10 ng/ml of murine macrophage-colony stimulating factor (R&D Systems) to induce macrophage differentiation. THP-1 cells and murine macrophages were seeded at 2.5 × 106 cells/well in 6-well plates, and human alveolar macrophages were seeded at 5.0 × 105 cells/well in 24-well plates, and cultured in RPMI-1640 containing 2.0 mM glutamine, 1.0 mM sodium pyruvate, 100 U/ml penicillin, 100 μg/ml streptomycin and 10% FBS at 37°C in a humidified incubator containing 5% CO2 in air.
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6

Macrophage and THP-1 Activation Analysis

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Mouse RAW264.7 macrophages and human THP-1 cells were obtained from the American Type Culture Collection (Manassas, VA, USA). Antibodies against inducible nitric oxide synthase (iNOS, #2982), cyclooxygenase-2 (COX-2 #4842), IL-1β (#12426), NLRP3 (#15101), caspase-1 (#3866), p-NF-κB (#3033), NF-κB (#8242), p-IκBα (#2859), IκBα (#4812), p-ERK (#4377), ERK1/2 (#9102), and SOD1 (#2770) were purchased from Cell Signaling (Beverly, MA, USA). Antibodies against caspase-1 (sc-398715), IL-18 (sc-7954), and GPx1/2 (sc-30147) were purchased from Santa Cruz (Santa Cruz, CA, USA).
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7

Foam Cell Formation from THP-1 Macrophages

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Human THP-1 cells obtained from American Type Culture Collection (ATCC; Manassas, VA, USA) were seeded on 35-mm Petri dishes at a density of 0.5×106 cells/mL in RPMI 1640 medium containing 10% FBS, 10 IU/mL penicillin and 10 µg/mL streptomycin and maintained at 37 °C in a humidified atmosphere containing 5% CO2. The THP-1 cells were differentiated into macrophages by adding 100 ng/mL PMA for 72 h. The macrophages were transformed into foam cells by incubating with 50 µg/mL oxLDL in serum-free RPMI 1640 medium containing 0.3% BSA for 48 h.
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8

Murine and Human Cancer Cell Lines Characterization

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BALB/c and C57BL/6 mice (female, 6-weeks-old) were purchased from Orient Bio and maintained under pathogen-free conditions. The animal study was reviewed and approved by the Institutional Animal Care and Use Committee (IACUC) of Sungkyunkwan University School of Medicine, which is accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC International) and abides by the Institute of Laboratory Animal Resources (ILAR) guide. Murine 4T1 (triple-negative breast cancer), murine TC1 (cervical cancer), and human THP-1 cells (American Type Culture Collection, ATCC) were cultured in RPMI medium (Thermo Fisher Scientific). Human C33a cervical cancer cells (ATCC) were cultured in Dulbecco’s Modified Eagle Medium (DMEM) medium (Thermo Fisher Scientific). The cell lines used in this study are not listed in the database of misidentified cell lines. The cell lines used in our study were tested to be free of mycoplasma contamination.
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9

Cultivation of M. avium 104 in THP-1 cells

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Mycobacterium avium subspecies hominissuis 104 (M. avium 104) was isolated from the blood of an AIDS patient and cultured on Middlebrook 7H10 agar supplemented with 10 % oleic acid, albumin, dextrose and catalase (OADC, Hardy Diagnostics, Santa Maria, CA) at 37 °C for 7 days. Human THP-1 cells were obtained from the American Type Culture Collection (Manassas, VA), cultivated in RPMI-1640 medium (Cellgro, Manassas, VA) supplemented with 10 % heat-inactivated fetal bovine serum, 2 mM L-glutamine and 25 mM HEPES, and incubated at 37 °C with 5 % CO2.
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10

Differentiation of THP-1 Monocytes to Macrophages

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Human THP-1 cells (American Type Culture Collection, Manassas, VA, USA) were seeded at a density of 1.0×105 cells per milliliter in RPMI 1640 medium (HyClone, Logan, UT, USA) containing 10% FBS (HyClone, Logan, UT, USA), 20 μg/mL penicillin and 20 μg/mL streptomycin (St Louis, MO, USA). The cells were maintained at 37°C in a humidified atmosphere containing 5% CO2. The cells were differentiated into macrophages by adding 100 ng/mL Phorbol-12-myristate-13-acetate (PMA) (La Jolla, CA, USA) for 72 hours in 96-well plates, 24-well plates and 35 mm Petri dishes.
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