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1.
J Cell Physiol ; 234(11): 20829-20846, 2019 11.
Artigo em Inglês | MEDLINE | ID: mdl-31049966

RESUMO

Maintenance of a balanced expression of the two isoforms of the transcription factor GATA-1, the full-length protein (GATA-1FL ) and a shorter isoform (GATA-1 S ), contributes to control hematopoiesis, whereas their dysregulation can alter the differentiation/proliferation potential of hematopoietic precursors thereby eventually leading to a variety of hematopoietic disorders. Although it is well established that these isoforms play opposite roles in these remarkable processes, most of the molecular pathways involved remain unknown. Here, we demonstrate that GATA-1FL and GATA-1S are able to differently influence intracellular redox states and reactive oxygen species (ROS) compartmentation in the erythroleukemic K562 cell line, thus shedding novel mechanistic insights into the processes of cell proliferation and apoptosis resistance in myeloid precursors. Furthermore, given the role played by ROS signaling as a strategy to escape apoptosis and evade cell-mediated immunity in myeloid cells, this study highlights a mechanism through which aberrant expression of GATA-1 isoforms could play a role in the leukemogenic process.


Assuntos
Compartimento Celular , Fator de Transcrição GATA1/metabolismo , Leucemia Mieloide/metabolismo , Leucemia Mieloide/patologia , Espécies Reativas de Oxigênio/metabolismo , Antioxidantes/metabolismo , Apoptose/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Grupo dos Citocromos b/metabolismo , DNA Mitocondrial/metabolismo , Complexo II de Transporte de Elétrons/metabolismo , Humanos , Células K562 , Oxirredução , Estresse Oxidativo/efeitos dos fármacos , Isoformas de Proteínas/metabolismo , Subunidades Proteicas/metabolismo , Quercetina/farmacologia , Succinato Desidrogenase/metabolismo
2.
ACS Appl Mater Interfaces ; 8(33): 21762-9, 2016 Aug 24.
Artigo em Inglês | MEDLINE | ID: mdl-27456037

RESUMO

Interactions between biomolecules and between substrates and biomolecules is a crucial issue in physics and applications to topics such as biotechnology and organic electronics. The efficiency of bio- and mechanical sensors, of organic electronics systems, and of a number of other devices critically depends on how molecules are deposited on a surface so that these acquire specific functions. Here, we tackle this vast problem by developing a coarse grained model of biomolecules having a recognition function, such as antibodies, capable to quantitatively describe in a simple manner essential phenomena: antigen-antibody and antibody substrate interactions. The model is experimentally tested to reproduce the results of a benchmark case, such as (1) gold surface functionalization with antibodies and (2) antibody-antigen immune-recognition function. The agreement between experiments and model prediction is excellent, thus unveiling the mechanism for antibody immobilization onto metals at the nanoscale in various functionalization schemes. These results shed light on the geometrical packing properties of the deposited molecules, and may open the way to a novel coarse-grained based approach to describe other processes where molecular packing is a key issue with applications in a huge number of fields from nano- to biosciences.

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