TY - JOUR
T1 - Impact of Toll-Like Receptor 4 Signaling in Necrotizing Enterocolitis
T2 - The State of the Science
AU - Mihi, Belgacem
AU - Good, Misty
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2019/3
Y1 - 2019/3
N2 - Necrotizing enterocolitis (NEC) remains a leading cause of preterm infant mortality. NEC is multifactorial and believed a consequence of intestinal immaturity, microbial dysbiosis, and an exuberant inflammatory response. Over the past decade, exaggerated Toll-like receptor 4 (TLR4) activity in the immature intestine of preterm neonates emerged as an inciting event preceding NEC. Increased TLR4 signaling in epithelial cells results in the initiation of an uncontrolled immune response and destruction of the mucosal barrier. This article discusses the state of the science of the molecular mechanisms involved in TLR4-mediated inflammation during NEC and the development of new therapeutic strategies to prevent NEC.
AB - Necrotizing enterocolitis (NEC) remains a leading cause of preterm infant mortality. NEC is multifactorial and believed a consequence of intestinal immaturity, microbial dysbiosis, and an exuberant inflammatory response. Over the past decade, exaggerated Toll-like receptor 4 (TLR4) activity in the immature intestine of preterm neonates emerged as an inciting event preceding NEC. Increased TLR4 signaling in epithelial cells results in the initiation of an uncontrolled immune response and destruction of the mucosal barrier. This article discusses the state of the science of the molecular mechanisms involved in TLR4-mediated inflammation during NEC and the development of new therapeutic strategies to prevent NEC.
KW - Epithelial cells
KW - Inflammation
KW - Necrotizing enterocolitis
KW - TLR4
UR - http://www.scopus.com/inward/record.url?scp=85058807979&partnerID=8YFLogxK
U2 - 10.1016/j.clp.2018.09.007
DO - 10.1016/j.clp.2018.09.007
M3 - Review article
C2 - 30771815
AN - SCOPUS:85058807979
SN - 0095-5108
VL - 46
SP - 145
EP - 157
JO - Clinics in Perinatology
JF - Clinics in Perinatology
IS - 1
ER -