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HB-EGF decelerates cell proliferation synergistically with TGFalpha in perinatal distal lung development.

作者信息

Minami Seigo, Iwamoto Ryo, Mekada Eisuke

机构信息

Department of Cell Biology, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.

出版信息

Dev Dyn. 2008 Jan;237(1):247-58. doi: 10.1002/dvdy.21398.

Abstract

Heparin-binding epidermal growth factor-like growth factor (HB-EGF) is a member of the EGF family of growth factors that is suggested to be involved in distal lung development. In HB-EGF null (HB(del/del)) newborns, a histopathologic analysis revealed abnormally thick saccular walls occurring from embryonic day 18.5 that reduced the terminal saccular space area. HB-EGF gene deletion resulted in a significant increase in cell proliferation, indicating that HB-EGF suppresses distal lung cell proliferation. Furthermore, an analysis of saccular morphology and proliferation in HB-EGF and transforming growth factor-alpha (TGFalpha) double-mutant newborns revealed that HB-EGF and TGFalpha function synergistically in this suppression. Finally, crosses between HB(del/del) mice and waved 2 mice, a hypomorphic EGF receptor (EGFR) mutant strain, suggest that HB-EGF and EGFR cooperate in this process. Thus, HB-EGF has a novel suppressive function that contributes to decelerating distal lung cell proliferation synergistically with TGFalpha through EGFR in perinatal distal lung development.

摘要

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