Show simple item record

dc.contributor.authorMartin, Ryan Danielen_US
dc.date.accessioned2017-04-13T01:49:53Z
dc.date.issued2013
dc.date.submitted2013
dc.identifier.urihttps://hdl.handle.net/2144/21213
dc.descriptionThesis (M.A.) PLEASE NOTE: Boston University Libraries did not receive an Authorization To Manage form for this thesis or dissertation. It is therefore not openly accessible, though it may be available by request. If you are the author or principal advisor of this work and would like to request open access for it, please contact us at open-help@bu.edu. Thank you.en_US
dc.description.abstractT1α (also known as Podoplanin), is a highly expressed gene found in lung alveolar type I (ATI) epithelial cells and in several other organ systems including lymphatic vessels and kidney. T1α is necessary for proper alveolar development and cell proliferation in the lung. It encodes an apical surface membrane protein involved in cell migration and morphogenesis. T1α also is upregulated at the leading edge of invasive tumors, and is used as a negative prognostic for remission-free recovery in cancer patients. Although T1α is known to interact with other cell membrane proteins, its molecular function and mechanism of action is not fully understood. To elucidate the molecular mechanisms of T1α regulation in normal lung alveolar development, we decided to identify T1α interacting proteins in lung cells. We performed mass spectrometry analysis on protein bands isolated from T1α co-immunoprecipitation, western blot, and immunofluorescence analyses. The mass spectrometry analysis of co-immunoprecipitated proteins with T1α resulted in the identification of several T1α interacting protein candidates, most notably Myh9. Myh9 is a member of a family of non-muscle myosins which is expressed in the lung epithelium, as well as in the kidneys’ podocytes, where its absence leads to a phenotype similar to reduced expression of T1α. Moreover, we confirmed the interaction of Myh9 with T1α by co-immunoprecipitation analysis in cell lysates derived from E10, a murine ATI-like cell line. Similarly, immunofluorescence staining showed that in the murine lung Myh9 and T1α display similar patterns of expression at the edge of ATI epithelial cells. Our results suggest that T1α interaction with Myh9 may play an important role in T1α-mediated cell migration and morphogenesis.en_US
dc.language.isoen_US
dc.publisherBoston Universityen_US
dc.subjectMedicineen_US
dc.subjectPathologyen_US
dc.subjectPodoplaninen_US
dc.titleT1alpha interacts with Myh9, a nonmuscle myosin, in type 1 lung epithelial cellsen_US
dc.typeThesis/Dissertationen_US
dc.description.embargo2031-01-01
etd.degree.nameMaster of Artsen_US
etd.degree.levelmastersen_US
etd.degree.disciplineMedicineen_US
etd.degree.grantorBoston Universityen_US


This item appears in the following Collection(s)

Show simple item record