JP2017505140A5 - - Google Patents
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- JP2017505140A5 JP2017505140A5 JP2016563912A JP2016563912A JP2017505140A5 JP 2017505140 A5 JP2017505140 A5 JP 2017505140A5 JP 2016563912 A JP2016563912 A JP 2016563912A JP 2016563912 A JP2016563912 A JP 2016563912A JP 2017505140 A5 JP2017505140 A5 JP 2017505140A5
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- 210000004027 cells Anatomy 0.000 claims 12
- 239000003795 chemical substances by application Substances 0.000 claims 8
- 230000000694 effects Effects 0.000 claims 6
- 230000004044 response Effects 0.000 claims 4
- 230000022131 cell cycle Effects 0.000 claims 3
- 238000005259 measurement Methods 0.000 claims 2
- 108040005185 1-phosphatidylinositol-3-kinase activity proteins Proteins 0.000 claims 1
- 102000010400 1-phosphatidylinositol-3-kinase activity proteins Human genes 0.000 claims 1
- 102100001248 AKT1 Human genes 0.000 claims 1
- 101700006234 AKT1 Proteins 0.000 claims 1
- 206010059512 Apoptosis Diseases 0.000 claims 1
- 210000000170 Cell Membrane Anatomy 0.000 claims 1
- 102000016736 Cyclins Human genes 0.000 claims 1
- 108050006400 Cyclins Proteins 0.000 claims 1
- FWBHETKCLVMNFS-UHFFFAOYSA-N DATI Chemical compound C1=CC(C(=N)N)=CC=C1C1=CC2=CC=C(C(N)=N)C=C2N1 FWBHETKCLVMNFS-UHFFFAOYSA-N 0.000 claims 1
- 231100000277 DNA damage Toxicity 0.000 claims 1
- 101700057458 Drice Proteins 0.000 claims 1
- 102100009835 EPHB2 Human genes 0.000 claims 1
- 101700024891 EPHB2 Proteins 0.000 claims 1
- RWSXRVCMGQZWBV-WDSKDSINSA-N Glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 claims 1
- 229960003180 Glutathione Drugs 0.000 claims 1
- 108010024636 Glutathione Proteins 0.000 claims 1
- 102100002658 H2BS1 Human genes 0.000 claims 1
- 101700021312 H2BS1 Proteins 0.000 claims 1
- 101700083887 MAPK1 Proteins 0.000 claims 1
- 210000001700 Mitochondrial Membranes Anatomy 0.000 claims 1
- 206010053961 Mitochondrial toxicity Diseases 0.000 claims 1
- 108010057466 NF-kappa B Proteins 0.000 claims 1
- 102000003945 NF-kappa B Human genes 0.000 claims 1
- 102000003992 Peroxidases Human genes 0.000 claims 1
- 108090000437 Peroxidases Proteins 0.000 claims 1
- 102000009738 Ribosomal Protein S6 Kinases Human genes 0.000 claims 1
- 108010034782 Ribosomal Protein S6 Kinases Proteins 0.000 claims 1
- 210000003705 Ribosomes Anatomy 0.000 claims 1
- 108040006844 SAP kinase activity proteins Proteins 0.000 claims 1
- 102000015031 SAP kinase activity proteins Human genes 0.000 claims 1
- ULHRKLSNHXXJLO-UHFFFAOYSA-L Yo-Pro-1 Chemical compound [I-].[I-].C1=CC=C2C(C=C3N(C4=CC=CC=C4O3)C)=CC=[N+](CCC[N+](C)(C)C)C2=C1 ULHRKLSNHXXJLO-UHFFFAOYSA-L 0.000 claims 1
- 238000004458 analytical method Methods 0.000 claims 1
- 230000006907 apoptotic process Effects 0.000 claims 1
- 230000003833 cell viability Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 238000004163 cytometry Methods 0.000 claims 1
- 239000007850 fluorescent dye Substances 0.000 claims 1
- 230000028709 inflammatory response Effects 0.000 claims 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 claims 1
- 150000002632 lipids Chemical class 0.000 claims 1
- 231100000296 mitochondrial toxicity Toxicity 0.000 claims 1
- 230000035699 permeability Effects 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 239000003642 reactive oxygen metabolite Substances 0.000 claims 1
- 241000894007 species Species 0.000 claims 1
- 230000003595 spectral Effects 0.000 claims 1
- 230000037327 stress response Effects 0.000 claims 1
Claims (11)
- 細胞に対する作用物質の効果を特徴付けるための方法であって、
a)種々の濃度系列の作用物質を細胞の集団のサンプルと接触させるステップ、
b)各サンプルについて及び各暴露濃度について集団の個々の細胞において2以上の表現型パラメータの各々を測定するステップ、
c)各パラメータについて及び各暴露について細胞の測定値の分布を得るステップ、
d)化合物に暴露していない細胞の測定値の分布を得るステップ、
e)ステップd)で得られた分布とステップc)で得られた各分布との間の非類似度を算出するステップ、
f)算出された非類似度を組み合わせて、マルチパラメトリック応答テンソルを形成するステップ
を含み、
ここで、マルチパラメトリック応答テンソルが、同じ方法で作成された他のフィンガープリントと直接比較することができる、細胞に対する作用物質の効果に特徴的なフィンガープリントである、方法。 - フィンガープリントを作成し記憶するために使用される、請求項1に記載の方法。
- フィンガープリントの比較を行うために使用される、請求項1に記載の方法。
- 比較が、in vivo効果を予測するために用いられる、請求項3に記載の方法。
- サイトメトリーによって個々の細胞において表現型パラメータを測定する、請求項1〜4のいずれか1項に記載の方法。
- 表現型パラメータが、細胞生存力、細胞周期段階、ミトコンドリア膜完全性、ミトコンドリア毒性、グルタチオン濃度、活性酸素種、還元種、細胞膜透過性、DNA損傷、ストレス応答マーカー、炎症応答マーカー、アポトーシスマーカー及び脂質ペルオキシダーゼのうちの2種以上を含む、請求項1〜5のいずれか1項に記載の方法。
- 表現型パラメータが、NF-kB、カスパーゼ、ERK、SAPK、PI3K、AKT、Bcl-ファミリータンパク質、p38、ATM、GSk3B、及びリボソームS6キナーゼのうちの1種以上を含む、請求項1〜6のいずれか1項に記載の方法。
- 表現型パラメータの1種が、細胞周期である、請求項1〜7のいずれか1項に記載の方法。
- 細胞の各集団が、複数の蛍光色素を用いて機能的に標識され、表現型パラメータが、前記標識された細胞の集団がサイトメトリー分析にかけられたときに生じるスペクトル発光シグナルの点で検出され、定量化される、請求項1〜8のいずれか1項に記載の方法。
- 表現型パラメータが細胞周期であり、HOECHST 33342、DRAQ5、YO-PRO-1 IODIDE、DAPI、CYTRAK ORANGE、サイクリン又はリン酸化ヒストンタンパク質の1種以上の点で定量化される、請求項1〜9のいずれか1項に記載の方法。
- 細胞に対する作用物質の効果に特徴的なフィンガープリントのバンクを作成するための方法であって、
請求項1〜10のいずれか1項に記載の方法により複数の作用物質の各々についてマルチパラメトリック応答テンソルを形成するステップであって、各マルチパラメトリック応答テンソルが、細胞に対する作用物質の効果に特徴的なフィンガープリントである、ステップ、
互いに比較し、同じ方法で作成された他の作用物質のフィンガープリントと比較することができるように、コンピュータ可読媒体にフィンガープリントを記憶するステップ
を含み、これにより、細胞に対する作用物質の効果に特徴的なフィンガープリントのデータベースを作成する、方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201461927247P | 2014-01-14 | 2014-01-14 | |
US61/927,247 | 2014-01-14 | ||
PCT/US2015/011441 WO2015109003A1 (en) | 2014-01-14 | 2015-01-14 | Identification of functional cell states |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2017505140A JP2017505140A (ja) | 2017-02-16 |
JP2017505140A5 true JP2017505140A5 (ja) | 2018-02-15 |
JP6606100B2 JP6606100B2 (ja) | 2019-11-13 |
Family
ID=52440877
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016563912A Active JP6606100B2 (ja) | 2014-01-14 | 2015-01-14 | 機能的細胞状態の同定 |
Country Status (12)
Country | Link |
---|---|
US (3) | US20150198584A1 (ja) |
EP (1) | EP3094974B1 (ja) |
JP (1) | JP6606100B2 (ja) |
KR (1) | KR102413041B1 (ja) |
AU (2) | AU2015206520B2 (ja) |
CA (1) | CA2972960C (ja) |
DK (1) | DK3094974T3 (ja) |
ES (1) | ES2728119T3 (ja) |
HK (1) | HK1231553A1 (ja) |
IL (1) | IL246734B (ja) |
SG (1) | SG11201705495XA (ja) |
WO (1) | WO2015109003A1 (ja) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20150198584A1 (en) * | 2014-01-14 | 2015-07-16 | Asedasciences Ag | Identification of functional cell states |
US10761011B2 (en) | 2015-02-24 | 2020-09-01 | The University Of Tokyo | Dynamic high-speed high-sensitivity imaging device and imaging method |
US11098275B2 (en) * | 2015-10-28 | 2021-08-24 | The University Of Tokyo | Analysis device |
US10824693B2 (en) | 2015-12-10 | 2020-11-03 | Reservoir Labs, Inc. | Systems and methods for selective expansive recursive tensor analysis |
US11205103B2 (en) | 2016-12-09 | 2021-12-21 | The Research Foundation for the State University | Semisupervised autoencoder for sentiment analysis |
CN110462372B (zh) * | 2017-05-25 | 2022-06-14 | 佛罗乔有限责任公司 | 大型多参数数据集的可视化、比较分析和自动差异检测 |
CN112638529B (zh) | 2018-06-13 | 2023-05-30 | 新克赛特株式会社 | 细胞计数的方法和系统 |
CA3139879A1 (en) | 2019-05-14 | 2020-11-19 | University Of Pittsburgh-Of The Commonwealth System Of Higher Education | System and method for characterizing cellular phenotypic diversity from multi-parameter cellular and sub-cellular imaging data |
EP4189065A4 (en) * | 2020-07-30 | 2024-08-28 | Allen Inst | SYSTEMS, DEVICES AND METHODS FOR SCREENING COMPOUNDS USING PREDICTIVE LABELING |
US20240337647A1 (en) | 2021-07-26 | 2024-10-10 | Asedasciences Ag | Improved methods for identification of functional cell states |
WO2023056481A1 (en) * | 2021-10-01 | 2023-04-06 | CAP Diagnostics, LLC, dba Pathnostics | Automated methods and systems for rapid identification of target particles |
US12105081B2 (en) * | 2021-10-20 | 2024-10-01 | Travera, Inc. | Treatment response assessment using normalized single cell measurements |
WO2024158752A1 (en) | 2023-01-23 | 2024-08-02 | Asedascience, Ag | Enhanced human-computer interaction systems |
Family Cites Families (16)
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US5544650A (en) * | 1988-04-08 | 1996-08-13 | Neuromedical Systems, Inc. | Automated specimen classification system and method |
WO1994016314A1 (en) | 1993-01-08 | 1994-07-21 | Coulter Corporation | Method of using preserved control cells in the calibration of fluorescent and light scatter measurements |
CA2196496A1 (en) | 1997-01-31 | 1998-07-31 | Stephen William Watson Michnick | Protein fragment complementation assay for the detection of protein-protein interactions |
US7166424B2 (en) | 1998-02-02 | 2007-01-23 | Odyssey Thera Inc. | Fragments of fluorescent proteins for protein fragment complementation assays |
US20050221280A1 (en) | 1998-02-02 | 2005-10-06 | Odyssey Thera, Inc. | Protein-protein interactions for pharmacological profiling |
US6801859B1 (en) | 1998-12-23 | 2004-10-05 | Rosetta Inpharmatics Llc | Methods of characterizing drug activities using consensus profiles |
US6998249B1 (en) | 1999-09-27 | 2006-02-14 | Pharmacia & Upjohn Company | Toxicity screening method |
US6656695B2 (en) | 2000-03-06 | 2003-12-02 | Bioseek, Inc. | Biomap characterization of biologically active agents |
EP1290428A1 (en) | 2000-06-02 | 2003-03-12 | Medicometrics APS | Method and system for classifying a biological sample |
US7146349B2 (en) * | 2000-11-06 | 2006-12-05 | International Business Machines Corporation | Network for describing multimedia information |
US20070087344A1 (en) | 2003-04-23 | 2007-04-19 | Bioseek, Inc. | Methods for characterizing signaling pathways and compounds that interact therewith |
US20070135997A1 (en) * | 2003-04-23 | 2007-06-14 | Evangelos Hytopoulos | Methods for analysis of biological dataset profiles |
WO2008134593A1 (en) * | 2007-04-25 | 2008-11-06 | President And Fellows Of Harvard College | Molecular circuits |
US20130226469A1 (en) | 2008-04-01 | 2013-08-29 | Purdue Research Foundation | Gate-free flow cytometry data analysis |
WO2009146036A2 (en) * | 2008-04-01 | 2009-12-03 | Purdue Research Foundation | Quantification of differences between measured values and statistical validation based on the differences |
US20150198584A1 (en) * | 2014-01-14 | 2015-07-16 | Asedasciences Ag | Identification of functional cell states |
-
2015
- 2015-01-14 US US14/596,957 patent/US20150198584A1/en not_active Abandoned
- 2015-01-14 ES ES15702063T patent/ES2728119T3/es active Active
- 2015-01-14 DK DK15702063.7T patent/DK3094974T3/da active
- 2015-01-14 JP JP2016563912A patent/JP6606100B2/ja active Active
- 2015-01-14 CA CA2972960A patent/CA2972960C/en active Active
- 2015-01-14 US US15/111,339 patent/US11137388B2/en active Active
- 2015-01-14 WO PCT/US2015/011441 patent/WO2015109003A1/en active Application Filing
- 2015-01-14 EP EP15702063.7A patent/EP3094974B1/en active Active
- 2015-01-14 AU AU2015206520A patent/AU2015206520B2/en active Active
- 2015-01-14 SG SG11201705495XA patent/SG11201705495XA/en unknown
- 2015-01-14 KR KR1020167022058A patent/KR102413041B1/ko active IP Right Grant
-
2016
- 2016-07-12 IL IL246734A patent/IL246734B/en active IP Right Grant
-
2017
- 2017-06-02 HK HK17104907.5A patent/HK1231553A1/zh unknown
-
2021
- 2021-06-28 AU AU2021204419A patent/AU2021204419A1/en not_active Abandoned
- 2021-08-05 US US17/394,521 patent/US11867690B2/en active Active
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