R
Ramesh Potla
Researcher at Cleveland Clinic
Publications - 7
Citations - 1259
Ramesh Potla is an academic researcher from Cleveland Clinic. The author has contributed to research in topics: Cellular respiration & Phosphorylation. The author has an hindex of 6, co-authored 7 publications receiving 1136 citations. Previous affiliations of Ramesh Potla include Cleveland State University.
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Journal ArticleDOI
Function of Mitochondrial Stat3 in Cellular Respiration
Joanna Wegrzyn,Ramesh Potla,Yong Joon Chwae,Naresh Babu V. Sepuri,Qifang Zhang,Thomas Koeck,Marta Derecka,Marta Derecka,Karol Szczepanek,Karol Szczepanek,Magdalena Szelag,Magdalena Szelag,Agnieszka Gornicka,Agnieszka Gornicka,Akira Moh,Shadi Moghaddas,Qun Chen,Santha Bobbili,Joanna Cichy,Jozef Dulak,Darren P. Baker,Alan Wolfman,Dennis J. Stuehr,Dennis J. Stuehr,Medhat O. Hassan,Xin-Yuan Fu,Narayan G. Avadhani,Jennifer I. Drake,Paul Fawcett,Edward J. Lesnefsky,Edward J. Lesnefsky,Andrew C. Larner +31 more
TL;DR: Data indicate that Stat3 is required for optimal function of the ETC, which may allow it to orchestrate responses to cellular homeostasis.
Journal ArticleDOI
Unexpected role of ceruloplasmin in intestinal iron absorption
Srujana Cherukuri,Srujana Cherukuri,Ramesh Potla,Ramesh Potla,Joydeep Sarkar,Joydeep Sarkar,Saul Nurko,Z. Leah Harris,Paul L. Fox,Paul L. Fox +9 more
TL;DR: Regulated relocalization of intestinal Cp may represent a fail-safe mechanism in which Cp shares with Heph responsibility for iron absorption under stress, suggesting a critical function of Cp in basolateral iron transport.
Journal ArticleDOI
Histone deacetylase activity is required to recruit RNA polymerase II to the promoters of selected interferon-stimulated early response genes.
TL;DR: To the authors' surprise, treatment of cells with the HDAC inhibitor, trichostatin A (TSA), inhibits selected interferon β (IFNβ)-stimulated immediate early genes that are activated by the transcription factors Stat1 and Stat2, suggesting that IRF9 functions to recruit RNA polymerase II to the promoter of interferons-stimulated genes.
Journal ArticleDOI
Tyk2 Tyrosine Kinase Expression Is Required for the Maintenance of Mitochondrial Respiration in Primary Pro-B Lymphocytes
Ramesh Potla,Thomas Koeck,Joanna Wegrzyn,Joanna Wegrzyn,Srujana Cherukuri,Kazuya Shimoda,Darren P. Baker,Janice C. Wolfman,Sarah M. Planchon,Christine Esposito,Brian D. Hoit,Jozef Dulak,Alan Wolfman,Dennis J. Stuehr,Dennis J. Stuehr,Andrew C. Larner,Andrew C. Larner +16 more
TL;DR: It is reported that Tyk2-null pro-B cells are markedly deficient in basal oxygen consumption and exhibit a significant decrease in steady-state cellular ATP levels compared to wild-type cells, and expression of a constitutively active Stat3 can restore the mitochondrial respiration in Tyk1-null cells treated with IFN-β.
Journal ArticleDOI
Activation of Tyk2 and Stat3 Is Required for the Apoptotic Actions of Interferon-β in Primary Pro-B Cells
Ana M. Gamero,Ana M. Gamero,Ramesh Potla,Ramesh Potla,Joanna Wegrzyn,Joanna Wegrzyn,Magdelena Szelag,Magdelena Szelag,Andrea E. Edling,Kazuya Shimoda,Daniel C. Link,Jozef Dulak,Darren P. Baker,Yoshinari Tanabe,Jason M. Grayson,Andrew C. Larner +15 more
TL;DR: An important role is demonstrated of Tyk2-mediated tyrosine phosphorylation of Stat3 in the ability of IFNβ to stimulate apoptosis of primary pro-B cells in primary murine interleukin-7-dependent pro- B cells.