ABSTRACT
The formation of the proper number of nephrons requires a tightly regulated balance between renal progenitor cell self-renewal and differentiation. The molecular pathways that regulate the transition from renal progenitor to renal vesicle are not well understood. Here, we show that Sall1interacts with the nucleosome remodeling and deacetylase complex (NuRD) to inhibit premature differentiation of nephron progenitor cells. Disruption of Sall1-NuRD in vivo in knock-in mice (ΔSRM) resulted in accelerated differentiation of nephron progenitors and bilateral renal hypoplasia. Transcriptional profiling of mutant kidneys revealed a striking pattern in which genes of the glomerular and proximal tubule lineages were either unchanged or upregulated, and those in the loop of Henle and distal tubule lineages were downregulated. These global changes in gene expression were accompanied by a significant decrease in THP-, NKCC2- and AQP1-positive loop of Henle nephron segments in mutant ΔSRM kidneys. These findings highlight an important function of Sall1-NuRD interaction in the regulation of Six2-positive multipotent renal progenitor cells and formation of the loop of Henle.
Subject(s)
Loop of Henle/embryology , Loop of Henle/metabolism , Mi-2 Nucleosome Remodeling and Deacetylase Complex/metabolism , Multipotent Stem Cells/cytology , Organogenesis , Transcription Factors/metabolism , Amino Acid Sequence , Animals , Biomarkers/metabolism , Cell Differentiation/genetics , Cell Lineage/genetics , Cell Proliferation/genetics , Gene Expression Regulation, Developmental , Gene Ontology , Homozygote , Kidney Tubules/metabolism , Loop of Henle/abnormalities , Mice , Multipotent Stem Cells/metabolism , Mutation/genetics , Organogenesis/genetics , Protein Binding/genetics , Transcription Factors/chemistry , Ureter/embryology , Ureter/metabolismABSTRACT
During nephrogenesis, POU domain class 3 transcription factor 3 (POU3F3 aka BRN1) is critically involved in development of distinct nephron segments, including the thick ascending limb of the loop of Henle (TAL). Deficiency of POU3F3 in knock-out mice leads to underdevelopment of the TAL, lack of differentiation of TAL cells, and perinatal death due to renal failure. Pou3f3L423P mutant mice, which were established in the Munich ENU Mouse Mutagenesis Project, carry a recessive point mutation in the homeobox domain of POU3F3. Homozygous Pou3f3L423P mutants are viable and fertile. The present study used functional, as well as qualitative and quantitative morphological analyses to characterize the renal phenotype of juvenile (12 days) and aged (60 weeks) homo- and heterozygous Pou3f3L423P mutant mice and age-matched wild-type controls. In both age groups, homozygous mutants vs. control mice displayed significantly smaller kidney volumes, decreased nephron numbers and mean glomerular volumes, smaller TAL volumes, as well as lower volume densities of the TAL in the kidney. No histological or ultrastructural lesions of TAL cells or glomerular cells were observed in homozygous mutant mice. Aged homozygous mutants displayed increased serum urea concentrations and reduced specific urine gravity, but no evidence of glomerular dysfunction. These results confirm the role of POU3F3 in development and function of the TAL and provide new evidence for its involvement in regulation of the nephron number in the kidney. Therefore, Pou3f3L423P mutant mice represent a valuable research model for further analyses of POU3F3 functions, or for nephrological studies examining the role of congenital low nephron numbers.
Subject(s)
Kidney/abnormalities , Kidney/growth & development , Mutation, Missense , Nerve Tissue Proteins/genetics , POU Domain Factors/genetics , Animals , Blood Pressure , Body Weight , Female , Kidney/metabolism , Loop of Henle/abnormalities , Loop of Henle/growth & development , Loop of Henle/metabolism , Male , Mice , Nephrons/abnormalities , Nephrons/growth & development , Nephrons/metabolism , Organ Size , RNA, Messenger/geneticsABSTRACT
Polycystic kidney disease (PKD) is an inherited disorder that is characterized by the accumulation of cysts in the renal parenchyma and progressive decline in renal function. Recent studies suggest that PKD arises from abnormalities of the primary cilium. We have previously shown that kidney-specific inactivation of the ciliogenic gene Kif3a during embryonic development produces kidney cysts and renal failure. Here, we used tamoxifen-inducible, kidney-specific gene targeting to inactivate Kif3a in the postnatal mouse kidney. Kidney-specific inactivation of Kif3a in newborn mice resulted in the loss of primary cilia and produced kidney cysts primarily in the loops of Henle, whereas inactivation in adult mice did not lead to the rapid development of cysts despite a comparable loss of primary cilia. The age-dependence and locations of the cysts suggested that cyst formation required increased rates of cell proliferation. To test this possibility, we stimulated cell proliferation in the adult kidney by inducing acute kidney injury and tubular regeneration. Acute kidney injury induced cyst formation in adult Kif3a mutant mice. Analysis of pre-cystic tubules in Kif3a mutant mice showed that the loss of cilia did not stimulate cell proliferation but instead resulted in aberrant planar cell polarity as manifested by abnormalities in the orientation of cell division. We conclude that primary cilia are required for the maintenance of planar cell polarity in the mammalian kidney and that acute kidney injury exacerbates cystic disease.
Subject(s)
Cysts/genetics , Cysts/pathology , Kinesins/genetics , Loop of Henle/abnormalities , Loop of Henle/pathology , Polycystic Kidney Diseases/genetics , Polycystic Kidney Diseases/pathology , Acute Disease , Animals , Cell Polarity , Cilia , Cysts/etiology , Humans , Kidney Diseases/chemically induced , Kidney Diseases/complications , Kinesins/antagonists & inhibitors , Mice , Mice, Transgenic , Polycystic Kidney Diseases/etiologyABSTRACT
During routine dissection of a left forearm, a simultaneous occurrence of Gantzers' muscles, Martin-Gruber anastomosis and nerve of Henle was observed in a 72 year old male. Both accessory muscle heads (Gantzers' muscles) originated from the medial epicondyle and coursed distally. The lateral accessory head crossed the ulnar artery, the Martin-Gruber anastomosis, and the branches of the median nerve to the flexors, the interosseous neurovascular bundle and the median nerve itself. The medial accessory head (Flexor Digitorum Profundus Accessorius) crossed the above structures except the last two. The Martin-Gruber anastomosis was a connection between the nerve to the Flexor Digitorum Profundus (a branch of the median nerve) and the ulnar nerve, which traversed posterior to the ulnar artery and two accessory muscle heads. The nerve of Henle originated from the ulnar nerve just proximal to joining the Martin-Gruber anastomosis, coursed distally with the ulnar artery, and supplied the skin of the distal forearm. These muscular and nervous anomalies are clinically significant since they are mutually related to one another and could compress the nerves or may be compromised during surgical procedures (AU)
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