Universität zu Köln

Bockmeyer, Clemens L., Wittig, Juliane, Saeuberlich, Karen, Selhausen, Philipp, Esser, Marc, Zeuschner, Philip ORCID: 0000-0001-8898-6588, Modde, Friedrich, Amann, Kerstin and Daniel, Christoph ORCID: 0000-0002-6803-4755 (2018). Recommendations for mRNA analysis of micro-dissected glomerular tufts from paraffin-embedded human kidney biopsy samples. BMC Mol. Biol., 19. LONDON: BIOMED CENTRAL LTD. ISSN 1471-2199

Full text not available from this repository.

Abstract

Background: Glomeruli are excellent pre-determined natural structures for laser micro-dissection. Compartmentspecific glomerular gene expression analysis of formalin-fixed paraffin-embedded renal biopsies could improve research applications. The major challenge for such studies is to obtain good-quality RNA from small amounts of starting material, as applicable for the analysis of glomerular compartments. In this work, we provide data and recommendations for an optimized workflow of glomerular mRNA analysis. Results: With a proper resolution of the camera and screen provided by the next generation of micro-dissection systems, we are able to separate parietal epithelial cells from glomerular tufts. Selected compartment-specific transcripts (WT1 and GLEPP1 for glomerular tuft as well as PAX2 for parietal epithelial cells) seem to be reliable discriminators for these micro-dissected glomerular substructures. Using the phenol-chloroform extraction and hemalaunstained sections (2 mu m), high amounts of Bowman's capsule transections (> 300) reveal sufficient RNA concentrations (> 300 ng mRNA) for further analysis. For comparison, in unstained sections from a number of 60 glomerular transections upwards, a minimum amount of 157 ng mRNA with a reasonable mRNA purity [A260/A280 ratio of 1.5 (1.4/1.7) median (25th/75th percentiles)] was reversely transcribed into cDNA. Comparing the effect of input RNA (20, 60, 150 and 300 micro-dissected glomerular transections), transcript expression of POLR2A significantly correlated when 60 and 150 laser micro-dissected glomerular transections were used for analysis. There was a lower inter-assay coefficient of variability for ADAMTS13, when at least 60 glomerular transections were used. According to the algorithms of geNormPlus and NormFinder, PGK1 and PPIA are more stable glomerular reference transcripts compared to GUSB, GAPDH, POLR2A, RPLPO, TBP, B2M, ACTB, 18SrRNA and HMBS. Conclusions: Our approach implements compartment-specific glomerular mRNA expression analysis into research applications, even regarding glomerular substructures like parietal epithelial cells. We recommend using of at least 60 micro-dissected unstained glomerular or 300 hemalaun-stained Bowman's capsule transections to obtain sufficient input mRNA for reproducible results. Hereby, the range of RNA concentrations in 60 micro-dissected glomeruli is low and appropriate normalization of -C-q values using our suggested reference transcripts (PGK1 and PPIA) allows compensation with respect to different amounts of RNA purity and quantity.

Item Type:	Journal Article
Creators:	Creators Email ORCID ORCID Put Code Bockmeyer, Clemens L. UNSPECIFIED UNSPECIFIED UNSPECIFIED Wittig, Juliane UNSPECIFIED UNSPECIFIED UNSPECIFIED Saeuberlich, Karen UNSPECIFIED UNSPECIFIED UNSPECIFIED Selhausen, Philipp UNSPECIFIED UNSPECIFIED UNSPECIFIED Esser, Marc UNSPECIFIED UNSPECIFIED UNSPECIFIED Zeuschner, Philip UNSPECIFIED orcid.org/0000-0001-8898-6588 UNSPECIFIED Modde, Friedrich UNSPECIFIED UNSPECIFIED UNSPECIFIED Amann, Kerstin UNSPECIFIED UNSPECIFIED UNSPECIFIED Daniel, Christoph UNSPECIFIED orcid.org/0000-0002-6803-4755 UNSPECIFIED
URN:	urn:nbn:de:hbz:38-192754
DOI:	10.1186/s12867-018-0103-x
Journal or Publication Title:	BMC Mol. Biol.
Volume:	19
Date:	2018
Publisher:	BIOMED CENTRAL LTD
Place of Publication:	LONDON
ISSN:	1471-2199
Language:	English
Faculty:	Unspecified
Divisions:	Unspecified
Subjects:	no entry
Uncontrolled Keywords:	Keywords Language GENE-EXPRESSION ANALYSIS; REAL-TIME PCR; LASER-CAPTURE MICRODISSECTION; POLYMERASE-CHAIN-REACTION; RENAL-CELL CARCINOMA; IGA NEPHROPATHY; ARCHIVAL TISSUE; NUCLEIC-ACIDS; DEGRADED RNA; RT-PCR Multiple languages Biochemistry & Molecular Biology Multiple languages
Refereed:	Yes
URI:	http://kups.ub.uni-koeln.de/id/eprint/19275