The kidney-specific proteome
The main function of the kidney is to maintain body homeostasis, regulating blood composition of water, electrolytes, solutes,
buffers as well as elimination of several organic compounds such as drugs and exogenous compounds. The kidney consists of
different cell types organized into sub-anatomical tissue structures with distinct functions in different segments of the nephron.
The transcriptome analysis shows that 68% of all human proteins (n=19628) are expressed in the kidney and 325 of these genes show an elevated expression in kidney compared to other tissue types.
An analysis of the genes with elevated expression in the
kidney with regard to biological function reveals that the corresponding proteins are part of the filtration diaphragm in
glomerulus, transport proteins responsible for specific absorption of various small molecules in the proximal tubule, proteins for
reabsorption of electrolyte to the blood and excretion of potassium to the urine in the distal tubules, and proteins involved in
salt and water transport in the collecting ducts.
- 53 kidney enriched genes
- Most of the enriched genes encode proteins involved in transport of small molecules
- 325 genes defined as elevated in the kidney
- Most group enriched genes shared expression with the liver
Figure 1. The distribution of all genes across the five categories based on transcript abundance in kidney as well as in all other tissues.
325 genes show some level of elevated expression in the kidney compared to other tissues. The three categories of genes with elevated expression in kidney compared to other organs are shown in Table 1. The list of tissue enriched genes (n=53) are well in-line with the function of the kidney.
Table 1. The genes with elevated expression in kidney
Number of genes
|At least five-fold higher mRNA levels in a particular tissue as compared to all other tissues
|At least five-fold higher mRNA levels in a group of 2-7 tissues
|At least five-fold higher mRNA levels in a particular tissue as compared to average levels in all tissues
|Total number of elevated genes in kidney
Table 2. The 12 genes with the highest level of enriched expression in kidney. "Predicted localization" shows the classification of each gene into three main classes: Secreted, Membrane, and Intracellular, where the latter consists of genes without any predicted membrane and secreted features. "mRNA (tissue)" shows the transcript level as TPM values, TS-score (Tissue Specificity score) corresponds to the score calculated as the fold change to the second highest tissue.
|transmembrane protein 174
|solute carrier family 12 (sodium/potassium/chloride transporter), member 1
|solute carrier family 22 (organic anion transporter), member 8
|solute carrier family 22 (organic anion/urate transporter), member 12
|solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
|potassium channel, inwardly rectifying subfamily J, member 1
|solute carrier family 12 (sodium/chloride transporter), member 3
|solute carrier family 7 (anionic amino acid transporter), member 13
|solute carrier family 22 (organic cation transporter), member 2
|solute carrier family 6 (neutral amino acid transporter), member 18
|nephrosis 2, idiopathic, steroid-resistant (podocin)
Some of the proteins predicted to be membrane-spanning are intracellular, e.g. in the Golgi or mitochondrial membranes, and some of the proteins predicted to be secreted can potentially be retained in a compartment belonging to the secretory pathway, such as the ER, or remain attached to the outer face of the cell membrane by a GPI anchor.
The kidney transcriptome
An analysis of the expression levels of each gene makes it possible to calculate the relative mRNA pool for each of the categories. The analysis shows that 87% of the mRNA molecules in the kidney correspond to housekeeping genes and only 6% of the mRNA pool corresponds to genes categorized to be either kidney enriched, group enriched, or enhanced. Thus, most of the transcriptional activity in the kidney relates to proteins with presumed housekeeping functions as they are found in all tissues and cells analyzed.
Protein expression of genes elevated in the kidney
In-depth analysis of the elevated genes in kidney using antibody-based protein profiling clearly shows that the main locations
of the kidney elevated proteins are in the glomeruli, proximal tubules, distal tubules and collecting ducts.
Proteins specifically expressed in glomerulus
The process of urine formation begins in the glomerulus, where an ultrafiltrate of plasma is formed, and the filtered fluid
enters the renal tubules. The filter consists of three layers: the fenestrated endothelium, the basement membrane, and the podocyte
slit diaphragm. The analysis of the glomerulus elevated proteins is well in line with the function of the glomerulus as a filtration
apparatus assembling a slit diaphragm. The list of kidney elevated proteins includes several well-known glomeruli associated
genes, such as podocin (NPHS2) and nephrin (NPHS1), well established
as proteins creating the filtration diaphragm making up a filter for large molecules
(Blum et al, 2007). In addition,
NEPH1, also known as
KIRREL, is present in the glomerulus as described before
(Donoviel et al, 2001). Interestingly, this latter protein is not identified as elevated
in kidney, since the placenta shows higher mRNA levels than kidney for this gene. The placenta also acts as a
filtration machinery for large and small molecules is therefore interesting
(Beall et al, 2005). The protein PODXL
has been reported to give a negative charge of the apical plasma membrane of the podocytes and also vascular endothelial cells in
general (Nielsen and McNagny, 2009). Another kidney elevated gene expressed in the glomerulus
Proteins specifically expressed in proximal tubule
Approximately 60% of the filtered Na+, Cl-, K+, Ca2+, and H2O and more than 90% of the filtered HCO3- are absorbed along the
proximal tubule. This is also the segment that normally reabsorbs virtually all the filtered glucose and amino acids.
An additional function is the secretion of numerous organic anions and cations. Most of the proteins elevated in the kidney are
localized to the proximal tubule, which is in line with the function of proximal tubule as a compartment for reabsorption of
small molecules back to the blood. This includes many genes coding for transport proteins responsible for specific adsorption of
various small molecules. In particular there are numerous members of the solute carrier family proteins (SLC) each with binding of
specific small molecules (He et al, 2009). It is also reassuring to find several enzymes
involved in digestion of proteins, such as peptidases, to allow adsorption of amino acids and peptides originating from proteins
transported into in the proximal tubule. The Gene Ontology analysis also supports these findings suggesting from the list of
elevated genes in proximal tubule, functions related to urate transport, cysteine transport, amino acid catabolic processes etc.
Examples of genes expressed in the proximal tubule are SLC22A8, localized in the basolateral
surface (blood), and SLC22A13, localized in the luminal surface (urine). AGMAT, BHMT, DPYS,
GGT1, HPD, HRSP12,
LRP2, PKLR and XPNPEP2 are all kidney
elevated genes expressed in the proximal tubule.
Proteins specifically expressed in the distal tubule
Both the distal tubule and collecting duct are the sites where critical regulatory hormones such as aldosterone and vasopressin
regulate acid and potassium excretion and determine final urinary concentration of K+, Na+, and Cl-. The distal tubule contains
the most abundant and most tissue specific protein in the kidney; the well-known uromodulin
(UMOD), although the specific function of this protein is yet somewhat unclear
(Bleyer et al, 2011). Similarly, the well-known calbindin
(CALB1) is also elevated in the distal tubules. In addition, the list of kidney elevated genes contains several receptors for
electrolyte transport, including potassium, sodium, and calcium transporters, such as SLC12A1.
Again this is in line with the function of the distal tubule as responsible for reabsorption of electrolyte to the blood and
excretion of potassium to the urine. Another example of a gene expressed in the distal tubule is SLC12A3.
Proteins specifically expressed in collecting duct
There are two different cell types in the collecting duct: principal cells and intercalated cells. Principal cells are the main
site of salt and water transport, and intercalated cells are the key site for acid-base regulation. Examples of the genes
expressed in the collecting duct are the aquaporin 2 (AQP2), localized in the luminal surface, and
ATP6V0D2 localized only in the intercalated cells.
TMEM213 is also a kidney elevated gene expressed in the collecting ducts.
Genes shared between kidney and other tissues
There are 116 group enriched genes expressed in the kidney. Group enriched genes are defined as genes showing a 5-fold higher average level of mRNA expression in a group of 2-7 tissues, including kidney, compared to all other tissues.
In order to illustrate the relation of kidney tissue to other tissue types, a network plot was generated, displaying the number of commonly expressed genes between different tissue types.
Figure 2. An interactive network plot of the kidney enriched and group enriched genes connected to their respective enriched tissues (grey circles). Red nodes represent the number of kidney enriched genes and orange nodes represent the number of genes that are group enriched. The sizes of the red and orange nodes are related to the number of genes displayed within the node. Each node is clickable and results in a list of all enriched genes connected to the highlighted edges. The network is limited to group enriched genes in combinations of up to 3 tissues, but the resulting lists show the complete set of group enriched genes in the particular tissue.
The kidney shows a specific pattern of shared group enriched genes with the liver. A Gene Ontology-based analysis of these shared genes shows that the group enriched genes were associated with "metabolic process".
The network plot reveals that most group enriched genes are shared with the liver (n=31).
The kidney is a specialized tissue that plays a vital role in maintaining body homeostasis. The main functions can be categorized as follows:
- Maintenance of body composition: the kidney regulates the volume of fluid in the body; its osmolarity, electrolyte content, concentration and acidity by varying the amounts of water and ions excreted in the urine.
- Excretion of metabolic end products and foreign substances: the kidney excretes a number of products of metabolism, most notably urea, and a number of toxins and drugs.
- Production and secretion of enzymes and hormones: the kidney is a source for several important hormones such as renin, which catalyzes the formation of angiotensin, the key peptide for blood pressure regulation, erythropoietin, which regulates the production of red blood cells, and activated vitamin D3, which regulates body calcium and phosphate balance.
The kidneys form the first part of the urinary system and their principle function is to maintain homeostasis by the regulation of electrolytes and the acid-base balance. Kidney function is vital for regulating blood pressure and the kidneys are also a source for several important hormones such as erythropoietin, which regulates the production of red blood cells. Histologically, the renal parenchyma consists of four parts: glomeruli, tubules, interstitium and blood vessels. Glomeruli are complex vascular structures composed of a tuft of capillaries comprised of specialized endothelial, epithelial and mesangial cells arranged around a relatively thick basement membrane. The glomerulus arises from the afferent arteriole to form lobules then rejoin the vascular pole to drain into the efferent arteriole. Normally the lobules are poorly defined but highlighted in some disease processes. The tuft of capillaries lies within the lumen of the expanded proximal end of the nephron, or Bowman's space, which is lined on its parietal aspect by a layer of attenuated epithelial cells overlying a thick basement membrane. Together the epithelial cells and basement membrane comprise the Bowman's capsule. The function of the glomerulus is filtration of the blood that leads to the formation of urine.
A complex tubular system begins at the urinary pole (where urine is first formed in the Bowman's space) that extends to the renal papilla. The system comprises the proximal tubule, the loop of Henle, distal tubule and collecting duct. The proximal tubule consists of convoluted and straight portions, lined by tall columnar cells with abundant, acidophilic cytoplasm rich in structures for active fluid transport. The loop of Henle has thin descending and thick ascending portions lined by cuboidal and columnar cells. The distal tubule is narrower and shorter than the proximal tubule and lined by low cuboidal cells that do not display the deeply acidophilic, granular cytoplasm characteristic of the proximal tubule. Cuboidal cells with pale acidophilic cytoplasm and central nuclei line the collecting ducts.
The interstitium is more easily conceptualized as a space rather than a structure; it is visualized only when abnormal. The interstitium contains specialized interstitial cells and connective tissue elements. The larger renal blood vessels are structurally similar to those in other body sites.
The histology of human kidney including detailed images and information about the different cell types can be viewed in the Protein Atlas Histology Dictionary.
Here, the protein-coding genes expressed in the kidney are described and characterized, together with examples of immunohistochemically stained tissue sections that visualize protein expression patterns of proteins that correspond to genes with elevated expression in the kidney.
Transcript profiling and RNA-data analyses based on normal human tissues have been described previously (Fagerberg et al., 2013). Analyses of mRNA expression including over 99% of all human protein-coding genes was performed using deep RNA sequencing of 172 individual samples corresponding to 37 different human normal tissue types. RNA sequencing results of 9 fresh frozen tissues representing normal kidney was compared to 163 other tissue samples corresponding to 36 tissue types, in order to determine genes with elevated expression in kidney. A tissue-specific score, defined as the ratio between mRNA levels in kidney compared to the mRNA levels in all other tissues, was used to divide the genes into different categories of expression.
These categories include: genes with elevated expression in kidney, genes expressed in all tissues, genes with a mixed expression pattern, genes not expressed in kidney, and genes not expressed in any tissue. Genes with elevated expression in kidney were further sub-categorized as i) genes with enriched expression in kidney, ii) genes with group enriched expression including kidney and iii) genes with enhanced expression in kidney.
Human tissue samples used for protein and mRNA expression analyses were collected and handled in accordance with Swedish laws and regulation and obtained from the Department of Pathology, Uppsala University Hospital, Uppsala, Sweden as part of the sample collection governed by the Uppsala Biobank. All human tissue samples used in the present study were anonymized in accordance with approval and advisory report from the Uppsala Ethical Review Board.
Relevant links and publications
Uhlén M et al, 2015. Tissue-based map of the human proteome. Science
PubMed: 25613900 DOI: 10.1126/science.1260419
Yu NY et al, 2015. Complementing tissue characterization by integrating transcriptome profiling from the Human Protein Atlas and from the FANTOM5 consortium. Nucleic Acids Res.
PubMed: 26117540 DOI: 10.1093/nar/gkv608
Fagerberg L et al, 2014. Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. Mol Cell Proteomics.
PubMed: 24309898 DOI: 10.1074/mcp.M113.035600
Habuka M et al, 2014. The kidney transcriptome and proteome defined by transcriptomics and antibody-based profiling. PLoS One.
PubMed: 25551756 DOI: 10.1371/journal.pone.0116125
Histology dictionary - the kidney