Developmental Origins of Renal Connecting Tubule and Collecting Duct: Role of Aqp2+ Progenitor Cells
type: CreativeWork
description: The connecting tubule interconnects the nephron and collecting duct, which arise from kidney mesenchyme and the ureteric bud, respectively, to generate the functional tubular networks. The collecting duct is comprised of principal cells and intercalated cells, which bear different molecular signatures and regulate sodium/water and acid/base balance, respectively. The progenitor cells of the connecting tubule and the collecting duct remain virtually unknown. We generated two Aqp2 lineage tracing mouse models. In these models, Aqp2Cre transgene drives Cre expression by the Aqp2 promoter to exclusively either inactivate histone H3 K79 methyltransferase Dot1l (Dot1lf/f Aqp2Cre) or activate RFP in Aqp2 lineage cells during development (Aqp2Cre RFP). H3 K79methylation and RFP were used as the tracing markers. Kidney sections were examined by immunofluorescence staining combined with epifluorescence and confocal microscopy. Analyses of Dot1lf/f Aqp2Cre revealed that Dot1l ablation abolished H3 K79 methylation, which occurs in both principal and intercalated cells. These results suggest that Aqp2+ progenitor cells give rise to principal cells and intercalated cells in the absence of Dot1l function. With Aqp2Cre RFP mice, we not only confirmed that derivation of intercalated cells from Aqp2+ progenitor cells is not an artifact of Dot1l deletion, but also identified the origin and molecular identities of connecting tubules. Aqp2+ progenitors contribute to renal tubular interconnection by differentiating into various types of transitional cells in the connecting tubule to form three molecularly distinct segments: RFP+Aqp2+NCC-, RFP+Aqp2-NCC-, and RFP+Aqp2-NCC+. RFP+ indicates progenitors of Aqp2+ origin. Aqp2- represents the loss of the original Aqp2+ progenitors. NCC+is the signature of distal convoluted tubule, the last segment ofnephron linking to the connecting tubule. In summary, our study 1) highlights the molecular identity and the origin of novel and distinct connectin…
abstract: The connecting tubule interconnects the nephron and collecting duct, which arise from kidney mesenchyme and the ureteric bud, respectively, to generate the functional tubular networks. The collecting duct is comprised of principal cells and intercalated cells, which bear different molecular signatures and regulate sodium/water and acid/base balance, respectively. The progenitor cells of the connecting tubule and the collecting duct remain virtually unknown. We generated two Aqp2 lineage tracing mouse models. In these models, Aqp2Cre transgene drives Cre expression by the Aqp2 promoter to exclusively either inactivate histone H3 K79 methyltransferase Dot1l (Dot1lf/f Aqp2Cre) or activate RFP in Aqp2 lineage cells during development (Aqp2Cre RFP). H3 K79methylation and RFP were used as the tracing markers. Kidney sections were examined by immunofluorescence staining combined with epifluorescence and confocal microscopy. Analyses of Dot1lf/f Aqp2Cre revealed that Dot1l ablation abolished H3 K79 methylation, which occurs in both principal and intercalated cells. These results suggest that Aqp2+ progenitor cells give rise to principal cells and intercalated cells in the absence of Dot1l function. With Aqp2Cre RFP mice, we not only confirmed that derivation of intercalated cells from Aqp2+ progenitor cells is not an artifact of Dot1l deletion, but also identified the origin and molecular identities of connecting tubules. Aqp2+ progenitors contribute to renal tubular interconnection by differentiating into various types of transitional cells in the connecting tubule to form three molecularly distinct segments: RFP+Aqp2+NCC-, RFP+Aqp2-NCC-, and RFP+Aqp2-NCC+. RFP+ indicates progenitors of Aqp2+ origin. Aqp2- represents the loss of the original Aqp2+ progenitors. NCC+is the signature of distal convoluted tubule, the last segment ofnephron linking to the connecting tubule. In summary, our study 1) highlights the molecular identity and the origin of novel and distinct connectin…
author: Chen, Lihe
keywords: Aqp2, Progenitors, Kidney, Principal Cell, Intercalated Cell, Biochemistry, Biophysics, and Structural Biology, Medicine and Health Sciences
date published: 2015-05-01T07:00:00Z
date modified: 2026-07-24T05:50:38Z
provider: University of Texas Health Science Center at Houston
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Texas Health Science Center at Houston