Faculty Opinions recommendation of Conserved and divergent features of human and mouse kidney organogenesis.

Author(s):  
Andreas Schedl
2018 ◽  
Vol 29 (3) ◽  
pp. 785-805 ◽  
Author(s):  
Nils O. Lindström ◽  
Jill A. McMahon ◽  
Jinjin Guo ◽  
Tracy Tran ◽  
Qiuyu Guo ◽  
...  

Human kidney function is underpinned by approximately 1,000,000 nephrons, although the number varies substantially, and low nephron number is linked to disease. Human kidney development initiates around 4 weeks of gestation and ends around 34–37 weeks of gestation. Over this period, a reiterative inductive process establishes the nephron complement. Studies have provided insightful anatomic descriptions of human kidney development, but the limited histologic views are not readily accessible to a broad audience. In this first paper in a series providing comprehensive insight into human kidney formation, we examined human kidney development in 135 anonymously donated human kidney specimens. We documented kidney development at a macroscopic and cellular level through histologic analysis, RNA in situ hybridization, immunofluorescence studies, and transcriptional profiling, contrasting human development (4–23 weeks) with mouse development at selected stages (embryonic day 15.5 and postnatal day 2). The high-resolution histologic interactive atlas of human kidney organogenesis generated can be viewed at the GUDMAP database (www.gudmap.org) together with three-dimensional reconstructions of key components of the data herein. At the anatomic level, human and mouse kidney development differ in timing, scale, and global features such as lobe formation and progenitor niche organization. The data also highlight differences in molecular and cellular features, including the expression and cellular distribution of anchor gene markers used to identify key cell types in mouse kidney studies. These data will facilitate and inform in vitro efforts to generate human kidney structures and comparative functional analyses across mammalian species.


2010 ◽  
pp. P2-27-P2-27
Author(s):  
RE Forster ◽  
CL Lowmiller ◽  
GK Whitfield ◽  
CA Haussler ◽  
PW Jurutka ◽  
...  

2006 ◽  
Vol 55 (3) ◽  
pp. 275-285 ◽  
Author(s):  
Miriam C. Banas ◽  
W. Tony Parks ◽  
Kelly L. Hudkins ◽  
Bernhard Banas ◽  
Matthew Holdren ◽  
...  
Keyword(s):  

2008 ◽  
Vol 130 (5) ◽  
pp. 943-956 ◽  
Author(s):  
Britta Walter ◽  
Tanja Schlechter ◽  
Michaela Hergt ◽  
Irina Berger ◽  
Ilse Hofmann

Author(s):  
Godfrey C. Hoskins ◽  
Betty B. Hoskins

Metaphase chromosomes from human and mouse cells in vitro are isolated by micrurgy, fixed, and placed on grids for electron microscopy. Interpretations of electron micrographs by current methods indicate the following structural features.Chromosomal spindle fibrils about 200Å thick form fascicles about 600Å thick, wrapped by dense spiraling fibrils (DSF) less than 100Å thick as they near the kinomere. Such a fascicle joins the future daughter kinomere of each metaphase chromatid with those of adjacent non-homologous chromatids to either side. Thus, four fascicles (SF, 1-4) attach to each metaphase kinomere (K). It is thought that fascicles extend from the kinomere poleward, fray out to let chromosomal fibrils act as traction fibrils against polar fibrils, then regroup to join the adjacent kinomere.


Author(s):  
John J. Wolosewick

Classically, the male germinal epithelium is depicted as synchronously developing uninucleate spermatids conjoined by intercellular bridges. Recently, binucleate and multinucleate spermatids from human and mouse testis have been reported. The present paper describes certain developmental events in one type of binucleate spermatid in the seminiferous epithelium of the mouse.Testes of adult mice (ABP Jax) were removed from the animals after cervical dislocation and placed into 2.5% glutaraldehyde/Millonig's phosphate buffer (pH 7.2). Testicular capsules were gently split and separated, exposing the tubules. After 15 minutes the tissue was carefully cut into cubes (approx. 1mm), fixed for an additional 45 minutes and processed for electron microscopy.


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