Journal of Stem Cell Research & Therapy

Aqp2+ progenitors are the principal source of connecting tubule

7^th Annual Conference on Stem Cell and Regenerative Medicine

August 04-05, 2016 Manchester, UK

Wenzheng Zhang

Albany Medical College, USA

Scientific Tracks Abstracts: J Stem Cell Res Ther

Abstract:

Connecting tubule (CNT) interconnects nephron and collecting duct (CD), which arise from kidney mesenchyme and the branching ureteric epithelium, respectively, to generate the functional tubular networks. CNT is thought as a product of reciprocal induction between the adjoining segments. The identity of the ureteric progenitors contributing to CNT remains virtually unknown. Recently, we reported that Aqp2-expressing cells with disrupted Dot1l give rise to principal cells (PC) and intercalated cells (IC). However, whether such derivation occurs naturally and whether Aqp2+ progenitors contribute to CNT has never been addressed. Here, we generate a new mouse model (RAC) in which Aqp2 lineage is genetically traced by red fluorescence protein. With high-resolution image analysis, we demonstrate that Aqp2+ progenitors naturally give rise to not only PC and IC, but also several types of CNT cells. CNT can be divided into three molecularly distinct segments. These segments contain CNT/DCT transitional cells, which originate from Aqp2+ progenitors, but gain expression of NCC, a wellestablished DCT marker. Our study highlights the molecular identity and the origin of novel and distinct CNT segments and discovers Aqp2+ progenitors as one of the origins of various types of cells not only in the CD but also in the CNT. Therefore, our study reports a novel mouse model that faithfully traces Aqp2 lineage and demonstrates a novel function of Aqp2+ progenitors in CNT formation. The discovery of the CNT segments and Aqp2+ progenitors may facilitate their isolation and functional evaluation.

Biography :

Wenzheng Zhang is an Associate Professor in the University of Texas Medical School at Houston. He received his PhD. from MD. Anderson Cancer Center and postdoctoral training from Howard Hughes Medical Institute, Baylor College of Medicine. His research focuses on epigenetic mechanism of Na+ and water homeostasis, with a special emphasis on histone H3 K79 methyltransferase Dot1l and the epithelial Na+ channel. He created Af17 knockout and Dot1l conditional knockout mice. Recently, he began to study biomarkers and stem cells in kidney injury and repair. He has published >40 peer-reviewed papers and received funding from NIH, AHA and ASN.

Email: zhangw1@mail.amc.edu