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Published ahead of print on June 5, 2008, doi:10.1164/rccm.200707-1104OC

Am. J. Respir. Crit. Care Med., Volume 178, Number 4, August 2008, 389-398

A more recent version of this article appeared on August 15, 2008
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Submitted on July 25, 2007
Accepted on June 5, 2008

Role of Secretoglobin (SCGB) 3A2 in Lung Development

Reiko Kurotani1, Takeshi Tomita2, Qian Yang2, Bradley A Carlson3, Chi Chen2, and Shioko Kimura2*

1 Cardiovascular Research Institute, Yokohama City University, Kanazawa, Japan, 2 Laboratory of Metabolism, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA, 3 Section on the Molecular Biology of Selenium, Laboratory of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA

* To whom correspondence should be addressed. E-mail: kimuras{at}mail.nih.gov.

Rationale: Secretoglobin (SCGB) 3A2 was originally identified as a downstream target in lung for the homeodomain transcription factor NKX2-1, whose null mutation resulted in severely hypoplastic lungs. A very low level of SCGB3A2 is expressed in lungs at embryonic day (E) 11.5 during mouse development, which markedly increases by E16.5, the time when lung undergoes dramatic morphological changes, suggesting that SCGB3A2 may be involved in lung development in addition to a known role in lung inflammation. Objectives: To determine whether SCGB3A2 plays a role in lung development. Methods: To assess a potential role for SCGB3A2 during early lung development, wildtype and Nkx2-1-null fetal lungs of early developmental stages were subjected to ex vivo organ culture in the presence of SCGB3A2. Nkx2-1-null fetuses were exposed to SCGB3A2 during early organogenesis period through intravenous administration of this protein to Nkx2-1-heterozygous pregnant females carrying these null fetuses. Cultured lungs and fetal lungs were subjected to histological and immunohistochemical analyses. To assess a role for SCGB3A2 in late lung development, SCGB3A2 was administered to pregnant wild-type females during mid to late organogenesis stages, and the preterm pups and/or their lungs were evaluated for extent of maturity using breathing motion, gross morphology and histology of lungs, expression of gestational stage-specific genes and phospholipid profiles. Measurements and Main Results: SCGB3A2 significantly promoted both early and late stages of lung development. Conclusions: SCGB3A2 is a novel growth factor in lung.


Key words: secretoglobin 3A2, UGRP1, NKX2-1, fetal lung development, growth factor




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