Literature DB >> 11918729

Protein restriction in pregnancy is associated with increased apoptosis of mesenchymal cells at the start of rat metanephrogenesis.

Simon J M Welham1, Angela Wade, Adrian S Woolf.   

Abstract

BACKGROUND: In rats, offspring born to mothers supplied low protein diets during pregnancy have fewer glomeruli than normal. We hypothesized that such nephron deficits are associated with altered cell turnover in the metanephros, the embryonic precursor of the adult kidney.
METHODS: Wistar rats were supplied with one of three isocaloric diets from day 0 of pregnancy: control (18% protein) or low protein (9% or 6%) diets. All had a normal chow after birth. Groups were compared by multilevel statistical modeling.
RESULTS: At two weeks postnatally, when nephrogenesis has finished, controls had 16.8 x 103 +/- 0.7 x 10(3) (mean +/- SEM) glomeruli/kidney, whereas offspring exposed to 9% diet had 5.1 x 10(3) +/- 1.2 x 10(3) fewer and those exposed to 6% diet had 6.9 x 10(3) +/- 1.7 x 10(3) fewer glomeruli/kidney (P < 0.001, both diets). At embryonic day 13 (E13), when the metanephros has just formed, control metanephroi contained 2.35 x 10(4) +/- 0.15 x 10(4) cells, with no significant differences in low protein groups. At E15, when mesenchyme begins forming primitive nephrons but glomeruli are still absent, controls had 2.00 x 10(6) +/- 0.13 x 10(6) cells. E15 embryos exposed to 9% protein had 1.09 x 10(6) +/- 0.36 x 10(6) fewer cells/metanephros than controls, while those exposed to 6% diet had 1.45 x 10(6) +/- 0.37 x 10(6) fewer (P < 0.01, both diets). Apoptotic cells were detected by molecular (in-situ end-labeling) and morphological (propidium iodide staining) techniques. In all diets, apoptosis was noted in condensing mesenchyme (nephron precursors) and loose mesenchyme (interstitial precursors). Control E13 metanephroi had 63 +/- 7 apoptotic cells/mm2, whereas those exposed to 9% diet had an increase of 77 +/- 26 cells/mm2 (P < 0.01) and those exposed to 6% diet had an increase of 55 +/- 26 cells/mm2 (P < 0.05). By E15, apoptosis was similar in all groups but metanephric mitosis was significantly increased in the 6% protein diet group. No change was found in the level of apoptosis in E13 mesonephroi.
CONCLUSIONS: Maternal low protein diets reduce final numbers of glomeruli in association with enhanced deletion of mesenchymal cells at the start of kidney development. Whether aberrant nephrogenesis is a direct effect from deletion of nephron precursors, or an indirect effect from loss of supportive interstitial precursors, requires further investigation.

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Year:  2002        PMID: 11918729     DOI: 10.1046/j.1523-1755.2002.00264.x

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  47 in total

1.  Effects of maternal hypercholesterolemia on pregnancy and development of offspring.

Authors:  Sônia Maria Alves De Assis; Antonio Carlos Seguro; Claudia Maria Barros Helou
Journal:  Pediatr Nephrol       Date:  2003-03-21       Impact factor: 3.714

Review 2.  Calcium signaling triggered by ouabain protects the embryonic kidney from adverse developmental programming.

Authors:  Georgiy R Khodus; Markus Kruusmägi; Juan Li; Xiao-Li Liu; Anita Aperia
Journal:  Pediatr Nephrol       Date:  2011-03-23       Impact factor: 3.714

3.  Prenatal corticosterone exposure results in altered AT1/AT2, nephron deficit and hypertension in the rat offspring.

Authors:  Reetu R Singh; Luise A Cullen-McEwen; Michelle M Kett; Wee-Ming Boon; John Dowling; John F Bertram; Karen M Moritz
Journal:  J Physiol       Date:  2007-01-04       Impact factor: 5.182

4.  The effect of intrauterine environment and low glomerular number on the histological changes in diabetic glomerulosclerosis.

Authors:  S E Jones; K E White; A Flyvbjerg; S M Marshall
Journal:  Diabetologia       Date:  2005-12-09       Impact factor: 10.122

5.  Apoptosis in the cortex of the developing mouse kidney.

Authors:  Jonathan G D Foley; Jonathan B L Bard
Journal:  J Anat       Date:  2002-12       Impact factor: 2.610

Review 6.  Mechanisms underlying the developmental origins of disease.

Authors:  Malgorzata S Martin-Gronert; Susan E Ozanne
Journal:  Rev Endocr Metab Disord       Date:  2012-06       Impact factor: 6.514

7.  Reduced nephron number in adult sheep, hypertensive as a result of prenatal glucocorticoid treatment.

Authors:  E M Wintour; K M Moritz; K Johnson; S Ricardo; C S Samuel; M Dodic
Journal:  J Physiol       Date:  2003-05-02       Impact factor: 5.182

8.  Fetal development and renal function in adult rats prenatally subjected to sodium overload.

Authors:  Henriqueta D Cardoso; Edjair V Cabral; Leucio D Vieira-Filho; Adalberto Vieyra; Ana D O Paixão
Journal:  Pediatr Nephrol       Date:  2009-07-15       Impact factor: 3.714

9.  The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation.

Authors:  Laura L Yates; Jenny Papakrivopoulou; David A Long; Paraskevi Goggolidou; John O Connolly; Adrian S Woolf; Charlotte H Dean
Journal:  Hum Mol Genet       Date:  2010-09-14       Impact factor: 6.150

10.  Ouabain protects against adverse developmental programming of the kidney.

Authors:  Juan Li; Georgiy R Khodus; Markus Kruusmägi; Padideh Kamali-Zare; Xiao-Li Liu; Ann-Christine Eklöf; Sergey Zelenin; Hjalmar Brismar; Anita Aperia
Journal:  Nat Commun       Date:  2010-07-27       Impact factor: 14.919

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