Distinct tube size is critical for the function of human tubular organs such as the lung, vascular system, and kidney. Aberrant tube sizes that arise during development can lead to devastating human illnesses such as Meckel kidney disease and polycystic kidney disease. However, the fundamental mechanisms that regulate tube size are still not well understood, preventing us from developing effective treatments for diseases caused by tube-size defects. Drosophila trachea provides a premier genetic system to investigate the fundamental mechanisms that regulate tube size. Mechanisms of tube-size control discovered in Drosophila trachea can be subsequently investigated in vertebrates, thereby extending our understanding of tube-size regulation in tubular organs in general. Recently, through a targeted RNAi knock down survey, we identified Expansion (Exp), an evolutionarily conserved and novel Smad-like protein, as an essential regulator of tube size in Drosophila trachea. Smad proteins generally function as mediators of Transforming Growth Factor-B (TGF-B) signaling. TGF- B signaling is known to control cell numbers within zebrafish cranial vessels, thereby regulating vessel diameter (Roman et al., 2002). However, our preliminary data indicated that TGF-B signaling and cell numbers were not involved in tube-size defects in exp mutants. Instead, the apical secretion of luminal proteins was defective, and the tracheal apical membrane was larger in exp mutants. In addition, phosphorylated MAP kinase (dp-Erk) levels were increased in exp mutants. Moreover, reducing Erk expression in exp mutants suppressed the observed tube-diameter defects. Other groups have shown that Epithelial Growth Factor (EGF) signaling phosphorylates Erk in Drosophila (Ohshiro et al., 2002) and that over-active EGF signaling expands tracheal tube diameter (Jeon et al., 2009), similar to our observations with exp mutants. Therefore, we hypothesize that Exp reduces EGF signaling to control the dynamic cellular processes required for tube-size regulation. We will test this hypothesis through the achievement of two specific Aims: (1) Identify the cellular processes that are regulated by Exp;2) Determine how Exp regulates EGF signaling to control tube-size. Through the proposed experiments, we expect to define a novel role for Smad family proteins in regulating signaling pathways and downstream dynamic cellular processes to control tube-size. We expect that the results from the proposed study will advance the understanding of how tubes acquire their distinct sizes in tubular organs in Drosophila, and many mechanisms will be shared with other organisms, including vertebrates. Ultimately, such knowledge has the potential to provide novel targets for developing treatments for human diseases caused by tube-size defects.

Public Health Relevance

Since many developmental mechanisms are well conserved between invertebrates and vertebrates, the results from our research will be beneficial for a greater understanding of the tubular organogenesis in vertebrates, and potentially lead to new avenues to treat human disease caused by tube-size defects.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15GM100369-01A1
Application #
8433039
Study Section
Development - 1 Study Section (DEV1)
Program Officer
Hoodbhoy, Tanya
Project Start
2013-04-01
Project End
2016-03-31
Budget Start
2013-04-01
Budget End
2016-03-31
Support Year
1
Fiscal Year
2013
Total Cost
$324,338
Indirect Cost
$97,338
Name
Oakland University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
041808262
City
Rochester
State
MI
Country
United States
Zip Code
48309
Iordanou, Ekaterini; Chandran, Rachana R; Yang, Yonghua et al. (2014) The novel Smad protein Expansion regulates the receptor tyrosine kinase pathway to control Drosophila tracheal tube size. Dev Biol 393:93-108