A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis
Copyright © 2021 International Society of Nephrology. Published by Elsevier Inc. All rights reserved..
Apolipoprotein L1 (APOL1)-associated focal segmental glomerulosclerosis (FSGS) is the dominant form of FSGS in Black individuals. There are no targeted therapies for this condition, in part because the molecular mechanisms underlying APOL1's pathogenic contribution to FSGS are incompletely understood. Studying the transcriptomic landscape of APOL1 FSGS in patient kidneys is an important way to discover genes and molecular behaviors that are unique or most relevant to the human disease. With the hypothesis that the pathology driven by the high-risk APOL1 genotype is reflected in alteration of gene expression across the glomerular transcriptome, we compared expression and co-expression profiles of 15,703 genes in 16 Black patients with FSGS at high-risk vs 14 Black patients with a low-risk APOL1 genotype. Expression data from APOL1-inducible HEK293 cells and normal human glomeruli were used to pursue genes and molecular pathways uncovered in these studies. We discovered increased expression of APOL1 and nine other significant differentially expressed genes in high-risk patients. This included stanniocalcin, which has a role in mitochondrial and calcium-related processes along with differential correlations between high- and low-risk APOL1 and metabolism pathway genes. There were similar correlations with extracellular matrix- and immune-related genes, but significant loss of co-expression of mitochondrial genes in high-risk FSGS, and an NF-κB-down regulating gene, NKIRAS1, as the most significant hub gene with strong differential correlations with NDUF family (mitochondrial respiratory genes) and immune-related (JAK-STAT) genes. Thus, differences in mitochondrial gene regulation appear to underlie many differences observed between high- and low-risk Black patients with FSGS.
Errataetall: |
CommentIn: Kidney Int. 2022 Jul;102(1):16-19. - PMID 35738828 |
---|---|
Medienart: |
E-Artikel |
Erscheinungsjahr: |
2022 |
---|---|
Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:102 |
---|---|
Enthalten in: |
Kidney international - 102(2022), 1 vom: 28. Juli, Seite 136-148 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
McNulty, Michelle T [VerfasserIn] |
---|
Links: |
---|
Themen: |
APOL1 protein, human |
---|
Anmerkungen: |
Date Completed 27.06.2022 Date Revised 03.07.2023 published: Print-Electronic CommentIn: Kidney Int. 2022 Jul;102(1):16-19. - PMID 35738828 Citation Status MEDLINE |
---|
doi: |
10.1016/j.kint.2021.10.041 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM334653002 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM334653002 | ||
003 | DE-627 | ||
005 | 20231225224148.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2022 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.kint.2021.10.041 |2 doi | |
028 | 5 | 2 | |a pubmed24n1115.xml |
035 | |a (DE-627)NLM334653002 | ||
035 | |a (NLM)34929253 | ||
035 | |a (PII)S0085-2538(21)01149-2 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a McNulty, Michelle T |e verfasserin |4 aut | |
245 | 1 | 2 | |a A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis |
264 | 1 | |c 2022 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 27.06.2022 | ||
500 | |a Date Revised 03.07.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a CommentIn: Kidney Int. 2022 Jul;102(1):16-19. - PMID 35738828 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2021 International Society of Nephrology. Published by Elsevier Inc. All rights reserved. | ||
520 | |a Apolipoprotein L1 (APOL1)-associated focal segmental glomerulosclerosis (FSGS) is the dominant form of FSGS in Black individuals. There are no targeted therapies for this condition, in part because the molecular mechanisms underlying APOL1's pathogenic contribution to FSGS are incompletely understood. Studying the transcriptomic landscape of APOL1 FSGS in patient kidneys is an important way to discover genes and molecular behaviors that are unique or most relevant to the human disease. With the hypothesis that the pathology driven by the high-risk APOL1 genotype is reflected in alteration of gene expression across the glomerular transcriptome, we compared expression and co-expression profiles of 15,703 genes in 16 Black patients with FSGS at high-risk vs 14 Black patients with a low-risk APOL1 genotype. Expression data from APOL1-inducible HEK293 cells and normal human glomeruli were used to pursue genes and molecular pathways uncovered in these studies. We discovered increased expression of APOL1 and nine other significant differentially expressed genes in high-risk patients. This included stanniocalcin, which has a role in mitochondrial and calcium-related processes along with differential correlations between high- and low-risk APOL1 and metabolism pathway genes. There were similar correlations with extracellular matrix- and immune-related genes, but significant loss of co-expression of mitochondrial genes in high-risk FSGS, and an NF-κB-down regulating gene, NKIRAS1, as the most significant hub gene with strong differential correlations with NDUF family (mitochondrial respiratory genes) and immune-related (JAK-STAT) genes. Thus, differences in mitochondrial gene regulation appear to underlie many differences observed between high- and low-risk Black patients with FSGS | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a focal segmental glomerular sclerosis | |
650 | 4 | |a gene expression | |
650 | 4 | |a glomerulus | |
650 | 4 | |a mitochondria | |
650 | 4 | |a nephrotic syndrome | |
650 | 7 | |a APOL1 protein, human |2 NLM | |
650 | 7 | |a Apolipoprotein L1 |2 NLM | |
700 | 1 | |a Fermin, Damian |e verfasserin |4 aut | |
700 | 1 | |a Eichinger, Felix |e verfasserin |4 aut | |
700 | 1 | |a Jang, Dongkeun |e verfasserin |4 aut | |
700 | 1 | |a Kretzler, Matthias |e verfasserin |4 aut | |
700 | 1 | |a Burtt, Noël P |e verfasserin |4 aut | |
700 | 1 | |a Pollak, Martin R |e verfasserin |4 aut | |
700 | 1 | |a Flannick, Jason |e verfasserin |4 aut | |
700 | 1 | |a Weins, Astrid |e verfasserin |4 aut | |
700 | 1 | |a Friedman, David J |e verfasserin |4 aut | |
700 | 0 | |a Nephrotic Syndrome Study Network (NEPTUNE) |e verfasserin |4 aut | |
700 | 1 | |a Sampson, Matthew G |e verfasserin |4 aut | |
700 | 1 | |a Dell, K |e investigator |4 oth | |
700 | 1 | |a Sedor, J |e investigator |4 oth | |
700 | 1 | |a Schachere, M |e investigator |4 oth | |
700 | 1 | |a Negrey, J |e investigator |4 oth | |
700 | 1 | |a Lemley, K |e investigator |4 oth | |
700 | 1 | |a Silesky, B |e investigator |4 oth | |
700 | 1 | |a Srivastava, T |e investigator |4 oth | |
700 | 1 | |a Garrett, A |e investigator |4 oth | |
700 | 1 | |a Sethna, C |e investigator |4 oth | |
700 | 1 | |a Laurent, K |e investigator |4 oth | |
700 | 1 | |a Canetta, P |e investigator |4 oth | |
700 | 1 | |a Pradhan, A |e investigator |4 oth | |
700 | 1 | |a Greenbaum, L |e investigator |4 oth | |
700 | 1 | |a Wang, C |e investigator |4 oth | |
700 | 1 | |a Kang, C |e investigator |4 oth | |
700 | 1 | |a Adler, S |e investigator |4 oth | |
700 | 1 | |a LaPage, J |e investigator |4 oth | |
700 | 1 | |a Athavale, A |e investigator |4 oth | |
700 | 1 | |a Itteera, M |e investigator |4 oth | |
700 | 1 | |a Atkinson, M |e investigator |4 oth | |
700 | 1 | |a Dell, T |e investigator |4 oth | |
700 | 1 | |a Fervenza, F |e investigator |4 oth | |
700 | 1 | |a Hogan, M |e investigator |4 oth | |
700 | 1 | |a Lieske, J |e investigator |4 oth | |
700 | 1 | |a Chernitskiy, V |e investigator |4 oth | |
700 | 1 | |a Kaskel, F |e investigator |4 oth | |
700 | 1 | |a Ross, M |e investigator |4 oth | |
700 | 1 | |a Flynn, P |e investigator |4 oth | |
700 | 1 | |a Kopp, J |e investigator |4 oth | |
700 | 1 | |a Blake, J |e investigator |4 oth | |
700 | 1 | |a Trachtman, H |e investigator |4 oth | |
700 | 1 | |a Zhdanova, O |e investigator |4 oth | |
700 | 1 | |a Modersitzki, F |e investigator |4 oth | |
700 | 1 | |a Vento, S |e investigator |4 oth | |
700 | 1 | |a Lafayette, R |e investigator |4 oth | |
700 | 1 | |a Mehta, K |e investigator |4 oth | |
700 | 1 | |a Gadegbeku, C |e investigator |4 oth | |
700 | 1 | |a Quinn-Boyle, S |e investigator |4 oth | |
700 | 1 | |a Hladunewich, M |e investigator |4 oth | |
700 | 1 | |a Reich, H |e investigator |4 oth | |
700 | 1 | |a Ling, P |e investigator |4 oth | |
700 | 1 | |a Romano, M |e investigator |4 oth | |
700 | 1 | |a Fornoni, A |e investigator |4 oth | |
700 | 1 | |a Bidot, C |e investigator |4 oth | |
700 | 1 | |a Kretzler, M |e investigator |4 oth | |
700 | 1 | |a Gipson, D |e investigator |4 oth | |
700 | 1 | |a Williams, A |e investigator |4 oth | |
700 | 1 | |a Klida, C |e investigator |4 oth | |
700 | 1 | |a Derebail, V |e investigator |4 oth | |
700 | 1 | |a Gibson, K |e investigator |4 oth | |
700 | 1 | |a Cole, E |e investigator |4 oth | |
700 | 1 | |a Ormond-Foster, J |e investigator |4 oth | |
700 | 1 | |a Holzman, L |e investigator |4 oth | |
700 | 1 | |a Meyers, K |e investigator |4 oth | |
700 | 1 | |a Kallem, K |e investigator |4 oth | |
700 | 1 | |a Swenson, A |e investigator |4 oth | |
700 | 1 | |a Sambandam, K |e investigator |4 oth | |
700 | 1 | |a Wang, Z |e investigator |4 oth | |
700 | 1 | |a Rogers, M |e investigator |4 oth | |
700 | 1 | |a Jefferson, A |e investigator |4 oth | |
700 | 1 | |a Hingorani, S |e investigator |4 oth | |
700 | 1 | |a Tuttle, K |e investigator |4 oth | |
700 | 1 | |a Bray, M |e investigator |4 oth | |
700 | 1 | |a Pao, E |e investigator |4 oth | |
700 | 1 | |a Cooper, A |e investigator |4 oth | |
700 | 1 | |a Lin, J J |e investigator |4 oth | |
700 | 1 | |a Baker, Stefanie |e investigator |4 oth | |
700 | 1 | |a Kretzler, M |e investigator |4 oth | |
700 | 1 | |a Barisoni, L |e investigator |4 oth | |
700 | 1 | |a Bixler, J |e investigator |4 oth | |
700 | 1 | |a Desmond, H |e investigator |4 oth | |
700 | 1 | |a Eddy, S |e investigator |4 oth | |
700 | 1 | |a Fermin, D |e investigator |4 oth | |
700 | 1 | |a Gadegbeku, C |e investigator |4 oth | |
700 | 1 | |a Gillespie, B |e investigator |4 oth | |
700 | 1 | |a Gipson, D |e investigator |4 oth | |
700 | 1 | |a Holzman, L |e investigator |4 oth | |
700 | 1 | |a Kurtz, V |e investigator |4 oth | |
700 | 1 | |a Larkina, M |e investigator |4 oth | |
700 | 1 | |a Li, S |e investigator |4 oth | |
700 | 1 | |a Li, S |e investigator |4 oth | |
700 | 1 | |a Lienczewski, C C |e investigator |4 oth | |
700 | 1 | |a Liu, J |e investigator |4 oth | |
700 | 1 | |a Mainieri, T |e investigator |4 oth | |
700 | 1 | |a Mariani, L |e investigator |4 oth | |
700 | 1 | |a Sampson, M |e investigator |4 oth | |
700 | 1 | |a Sedor, J |e investigator |4 oth | |
700 | 1 | |a Smith, A |e investigator |4 oth | |
700 | 1 | |a Williams, A |e investigator |4 oth | |
700 | 1 | |a Zee, J |e investigator |4 oth | |
700 | 1 | |a Avila-Casado, Carmen |e investigator |4 oth | |
700 | 1 | |a Bagnasco, Serena |e investigator |4 oth | |
700 | 1 | |a Gaut, Joseph |e investigator |4 oth | |
700 | 1 | |a Hewitt, Stephen |e investigator |4 oth | |
700 | 1 | |a Hodgin, Jeff |e investigator |4 oth | |
700 | 1 | |a Lemley, Kevin |e investigator |4 oth | |
700 | 1 | |a Mariani, Laura |e investigator |4 oth | |
700 | 1 | |a Palmer, Matthew |e investigator |4 oth | |
700 | 1 | |a Rosenberg, Avi |e investigator |4 oth | |
700 | 1 | |a Royal, Virginie |e investigator |4 oth | |
773 | 0 | 8 | |i Enthalten in |t Kidney international |d 1972 |g 102(2022), 1 vom: 28. Juli, Seite 136-148 |w (DE-627)NLM000007188 |x 1523-1755 |7 nnns |
773 | 1 | 8 | |g volume:102 |g year:2022 |g number:1 |g day:28 |g month:07 |g pages:136-148 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.kint.2021.10.041 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 102 |j 2022 |e 1 |b 28 |c 07 |h 136-148 |