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Quantitative label-free mass spectrometry reveals content and signaling differences between neonatal and adult platelets.
Thom, Christopher S; Davenport, Patricia; Fazelinia, Hossein; Soule-Albridge, Erin; Liu, Zhi-Jian; Zhang, Haorui; Feldman, Henry A; Ding, Hua; Roof, Jennifer; Spruce, Lynn A; Ischiropoulos, Harry; Sola-Visner, Martha.
Afiliação
  • Thom CS; Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA. Electronic address: thomc@chop.edu.
  • Davenport P; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Fazelinia H; Proteomics Core, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Soule-Albridge E; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Liu ZJ; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Zhang H; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Feldman HA; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts, USA; Institutional Centers for Clinical and Translational Research, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Ding H; Proteomics Core, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Roof J; Proteomics Core, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Spruce LA; Proteomics Core, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Ischiropoulos H; Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA; Children's Hospital of Philadelphia Research Institute, Philadelphia, Pennsylvania, USA.
  • Sola-Visner M; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts, USA. Electronic address: Martha.sola-visner@childrens.harvard.edu.
J Thromb Haemost ; 22(5): 1447-1462, 2024 May.
Article em En | MEDLINE | ID: mdl-38160730
ABSTRACT

BACKGROUND:

Recent clinical studies have shown that transfusions of adult platelets increase morbidity and mortality in preterm infants. Neonatal platelets are hyporesponsive to agonist stimulation, and emerging evidence suggests developmental differences in platelet immune functions.

OBJECTIVES:

This study was designed to compare the proteome and phosphoproteome of resting adult and neonatal platelets.

METHODS:

We isolated resting umbilical cord blood-derived platelets from healthy full-term neonates (n = 8) and resting blood platelets from healthy adults (n = 6) and compared protein and phosphoprotein contents using data-independent acquisition mass spectrometry.

RESULTS:

We identified 4770 platelet proteins with high confidence across all samples. Adult and neonatal platelets were clustered separately by principal component analysis. Adult platelets were significantly enriched in immunomodulatory proteins, including ß2 microglobulin and CXCL12, whereas neonatal platelets were enriched in ribosomal components and proteins involved in metabolic activities. Adult platelets were enriched in phosphorylated GTPase regulatory enzymes and proteins participating in trafficking, which may help prime them for activation and degranulation. Neonatal platelets were enriched in phosphorylated proteins involved in insulin growth factor signaling.

CONCLUSION:

Using label-free data-independent acquisition mass spectrometry, our findings expanded the known neonatal platelet proteome and identified important differences in protein content and phosphorylation between neonatal and adult platelets. These developmental differences suggested enhanced immune functions for adult platelets and presence of molecular machinery related to platelet activation. These findings are important to understanding mechanisms underlying key platelet functions as well as the harmful effects of adult platelet transfusions given to preterm infants.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfoproteínas / Plaquetas / Transdução de Sinais / Proteômica / Sangue Fetal Limite: Adult / Female / Humans / Male / Newborn Idioma: En Revista: J Thromb Haemost Assunto da revista: HEMATOLOGIA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfoproteínas / Plaquetas / Transdução de Sinais / Proteômica / Sangue Fetal Limite: Adult / Female / Humans / Male / Newborn Idioma: En Revista: J Thromb Haemost Assunto da revista: HEMATOLOGIA Ano de publicação: 2024 Tipo de documento: Article
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