Fluorescence in situ hybridization showed that CRELD2 maps to human chromosome 22q13 (28). Multiple splice variants are expressed by CRELD2, which encode for many transcripts that likely produce multiple protein isoforms (α, β, γ, δ, ϵ, ζ) (28). Sequence analysis revealed that each isoform has several overlapping motifs; however, they differ from each other in that they contain either tandem arrays of EGF- and/or calcium- binding EGF domains, or EGF/calcium-binding EGF domains and furin cysteine-rich domains (28). In contrast, they all have a WE-rich domain unique to the CRELD protein family, which is conserved across species (17, 28). CRELD2 is also highly conserved in orthologs and is identified in many vertebrates (28). There is also a murine Creld2 ortholog with 69% identity to human CRELD2 (17). Notably, the mouse Creld2 gene presumably corresponds to the human CRELD2α gene (14).

As the members of the CRELD family, CRELD1 and CRELD2 exhibit 51% homology in the nucleic acid sequences of the coding regions. At the amino acid level, they were 38% identical and 51% similar (17). Notably, CRELD1 and CRELD2 generally share similar domain structures, with a highly conserved WE region that has not been found in any non-homologous members, which is considered the hallmark feature of the CRELD protein family, followed by variations in EGF domains (28). In contrast to CRELD1, which has two type III transmembrane domains at the carboxyl(C)-terminus that anchors the protein to the cell surface, CRELD2 does not have any predicted transmembrane domains (15, 17, 28). The C-terminus of CRELD2 contains four (R/H)EDL amino acids, which are well conserved across species, including REDL for human, mouse, and bovine, and HEDL for rat, chicken, Xenopus, and zebrafish (15) ( Figure 2A ). These amino acids are reportedly similar to the C-terminal amino acids in several ER-resident proteins, such as KDEL for GRP78 (62, 63) and RTDL for mesencephalic astrocyte-derived neurotrophic factor (MANF) (64–67) ( Figure 2B ). In fact, many ER-resident proteins have a C-terminal KDEL (Lys-Asp-Glu-Leu) motif, which is the canonical sequence for retention of the ER chaperone including GRP78, while RTDL and (R/H)EDL are variants of KDEL sequence with similar functions (15, 66, 68). Studies have demonstrated that CRELD2 is primarily localized to the ER and Golgi apparatus and can be secreted into the extracellular space upon cellular stimuli, particularly ER stress (14, 15). The four amino acids domain in the C-terminus of CRELD2 is considered essential for the retention and secretion of CRELD2, which will be our focus in subsequent sections. Notably, studies have revealed that the amino(N)-terminus of CRELD2 is critical for its translocation into the ER-Golgi apparatus, whereas the deletion of its C-terminal region has no effect on its accumulation in the perinuclear region (15). Additionally, CRELD2 reportedly has numerous CXXC motifs ( Figure 2C ), and the N-terminal CXXC motif possesses protein isomerase activity (16). This pair of active protein disulfide isomerase (PDI)-like cysteine residues, CXXC, can shuttle between the disulfide and dithiol forms, thereby catalyzing thiol-disulfide oxidation, reduction, and isomerization, which are critical for correct disulfide bond formation and/or arrangement if incorrect bonds are formed (16, 69, 70). Therefore, its PDI-like activity further supports the idea that CRELD2 might participate in the quality control of proteins in the ER.

The analysis of the upstream sequences of CRELD2 revealed a functional promoter region embedded within a large CpG island (28). In 2009, Oh-hashi et al. performed a genomic sequence analysis of the promoter region of the mouse Creld2 gene and identified a putative ER stress responsible element (ERSE; CGTGG-N9-ATTGG), which is highly conserved among different species (14) ( Figure 2D ). This conservation further indicates that CRELD2 may play a role in regulating cellular behavior during ER stress. They first identified that CRELD2 is predominantly localized in the ER and Golgi apparatus and is a novel ER stress-inducible gene (14). Specifically, in Neuro2a cells, Creld2 mRNA was induced by treatment with the ER-inducing chemical agents, namely thapsigargin (Tg, a well-known inhibitor of Ca²⁺-ATPase), tunicamycin (Tm, an inhibitor of protein glycosylation), and brefeldin A (BFA, an inhibitor of ER-Golgi transport) (14). Furthermore, luciferase reporter analyses revealed that ATF6 overexpression drastically induced Creld2 mRNA expression by directly binding to the ERSE of the Creld2 gene. Mutations in the mouse Creld2 promoter ERSE considerably decreased both basal activity and responsiveness toward ER stress stimuli (14).

Additionally, further studies confirmed that CRELD2 is responsive to ER stress stimuli. For example, neonatal rat cardiomyocytes treated with Tm significantly upregulated Creld2, as well as several other genes involved in ER stress. This upregulation was significantly attenuated by salubrinal and its derivatives, which are the inhibitors of ER stress (71). Additionally, mouse podocytes treated with either Tm or Tg for 24 h remarkably induced CRELD2 expression (72), indicating that the upregulation of CRELD2 induced by ER stress stimuli is a general and not cell-type-specific response. Moreover, in vivo studies also found that CRELD2 protein expression in the mouse liver was considerably induced 24 h after intraperitoneal injection of Tm (73). These results suggest that CRELD2 may be involved in the processing of proteins and may be a novel mediator in regulating the onset and progression of various ER stress-associated diseases.

CRELD2 is both an ER-resident protein and a secretory factor (14, 15). However, the mechanisms that regulate the intracellular transportation and secretion of CRELD2 are poorly understood. In 2011, Oh-hashi et al. found that the N-terminus of CRELD2 is necessary for its translocation into the ER-Golgi apparatus (15). Additionally, the disruption of the Golgi apparatus by BFA almost completely prevents CRELD2 secretion (15, 74), suggesting that CRELD2 might be secreted via the ER-Golgi apparatus. Moreover, the overexpression of dominant negative mutant Sar1, a component of cytoplasmic vesicle coat protein complex II (COPII), drastically suppressed the spontaneous secretion of CRELD2. Sar1 plays an essential role in early step in vesicle budding and regulating vesicular transport from the ER to the Golgi (75, 76), and this further supports that COPII-mediated transport from the ER to the Golgi apparatus is the main pathway for CRELD2 trafficking (15) ( Figure 3A ). Despite this evidence, further studies are warranted to comprehensively understand the mechanism that regulates cellular transport of CRELD2.

The conditions under which CRELD2 secretion is induced are still not comprehensively elucidated. However, both in vitro and in vivo studies have demonstrated that CRELD2 secretion is drastically induced upon ER stress. For example, cells subjected to ER stress by chemical agents such as Tm, Tg, and BFA, or by culturing cells in serum-free medium showed increased CRELD2 secretion (15, 73). In ER stress-related disease models, such as matrilin-3 (Matn3) and collagen type X alpha 1 chain (Col10a1) mutant growth plates, CRELD2 was also detectable at significant levels in the extracellular matrix (ECM) but not in wild-type controls (16). Additionally, CRELD2 is rapidly secreted when renal cells are subjected to ER stress in mouse models of podocyte ER stress-induced nephrotic syndrome (NS) and Tm- or I/R-induced acute kidney injury (AKI) (72). The observation that CRELD2 is an ER-resident protein and can be secreted under induced ER stress suggests that it might act as a multifunctional factor both in the ER-Golgi apparatus as well as in the extracellular space under normal and pathophysiological conditions.

Studies have revealed that the four-amino acid sequence (R/H)EDL in the C-terminal region of CRELD2 regulates its secretion. For example, in HEK293 cells, the modification of the C-terminal region, such as the deletion of four C-terminal amino acids from mouse CRELD2 or addition of tag-peptides to its C-terminus, drastically enhanced CRELD2 secretion (15). Additionally, the overexpression of wild-type GRP78, but not mutant GRP78 lacking the C-terminal KDEL sequence, remarkably enhanced CRELD2 secretion, whereas mutant CRELD2 at the C-terminus did not show any upregulation (15). Therefore, CRELD2 is a novel secretory factor regulated by GRP78, whereas the comprehensive molecular mechanism remains unresolved. However, the KDEL receptor (KDELR) competition hypothesis was also proposed (15, 16) ( Figures 3A, B ). The four highly conserved amino acids in CRELD2 are similar to the C-terminal amino acids in GRP78, which also possesses the well-known ER-resident signal sequence KDEL (62, 63). The secretion of many ER-resident proteins is restricted via this ER retention motif, facilitating retrieval transport from the Golgi apparatus via binding to KDELRs, which are located in the intermediate compartment or in the cis-Golgi apparatus, with high affinity (68, 77–84). Similarly, the putative ER retention motif REDL at the C-terminus enables CRELD2 to be retained in the ER (15). Under normal conditions, both REDL and KDEL trafficked to Golgi apparatus can bind with KDELRs, thereby efficiently transporting them back to the ER. However, during ER stress, the relative levels of multiple ER stress-inducible proteins such as GRP78 and CRELD2 are upregulated, whereas the relative expression of KDELRs are not increased (16, 85). Thus, GRP78, containing perfect ER retention motifs that have high affinity for the KDELRs, would compete with CRELD2, containing a motif that has a low binding affinity, thereby allowing CRELD2 to escape the ER and ultimately be secreted (15, 16) ( Figures 3A, B ).

Further studies have revealed that, additionally to GRP78, MANF can enhance CRELD2 secretion (86). Similar to CRELD2, MANF has recently been identified as an ER stress-responsive protein (65–67, 85, 87–92). MANF possesses ER-resident motifs at its proximal C-terminus, RTDL, which regulates MANF secretion upon ER stress (64–67). Studies have revealed that in both HEK293 and COS7 cell lines, co-transfection with CRELD2 and MANF remarkably increased the secretion of CRELD2 into the extracellular space (86). This effect highly depends on both of the four C-terminal amino acid sequences (RTDL in MANF and REDL in CRELD2) because the deletion of these four C-terminal amino acids terminated the increased secretion of CRELD2 induced by the co-expression of MANF (86). Notably, the data showed that the increase in CRELD2 secretion by MANF overexpression might not be simply due to the expression of intrinsic ER-resident chaperones or a result of competition between the two proteins for KDELRs (86). Further studies have revealed that the overexpression of mouse cerebral dopamine neurotrophic factor (CDNF), a paralogous protein of MANF that also contains the KDEL-like motif of the ER retrieval signal at its C-terminus, hardly affected the co-transfected CRELD2 secretion (93). Moreover, the inhibition of vacuolar ATPase, a proton pump that regulates the pH of several intracellular compartments, remarkably induced CRELD2 secretion without relying on its C-terminal structure (74). These results provide valuable insights into the mechanism of CRELD2 secretion regulation, which warrants further investigation.

Several studies have confirmed the ubiquitous expression of CRELD2. In 2005, through northern blotting, Ortiz et al. first revealed that the high expression levels of CRELD2 were observed in the skeletal muscle, heart, liver, kidney, and placenta of human tissues (28). In 2006, Maslen et al. conducted intensive studies in different human tissues by combining both northern blot and RNA dot blot (28). They demonstrated that CRELD2 was ubiquitously expressed during development and in mature tissues, although a broad range of signal intensities were observed. Additionally, the most prominent signals of CRELD2 in adult tissues occur in pancreas, stomach, duodenum, salivary gland, thyroid gland, appendix, and trachea, which generally overlap with the expression pattern for CRELD1 (17, 28). However, in fetal tissues, CRELD2 is highly expressed in the lung, liver, thymus, spleen, and heart (28).

Additional to its expression pattern in humans, the ubiquitous expression of CRELD2 has been confirmed in rodents (73, 94). In 2018, Oh-hashi et al. evaluated the mRNA and protein expression patterns of CRELD2 in different adult mouse tissues (73). They found that the Creld2 mRNA was present in almost all tissues tested, including the brain, heart, lung, liver, spleen, kidney, stomach, and small intestine, but not in skeletal muscles. However, CRELD2 protein expression in the heart and skeletal muscle was negligible, and that in the brain was relatively low (73). To understand the discrepancy between CRELD2 mRNA and protein expression, they further examined the stability of CRELD2 protein in Neuro2a cells through treatment with the protein synthesis inhibitor cycloheximide and/or the proteasome inhibitor MG132 together with the ER stress agent Tg. However, the protein levels of CRELD2 were hardly affected by each treatment (73). Until now, of the reason for this discrepancy remains unclear, which may be important for us to further understand the characteristics and functions of CRELD2.

ER stress reportedly contributes to the onset and progression of multiple liver diseases including non-alcoholic fatty liver disease (NAFLD) and alcoholic liver diseases (3, 111–116). Although CRELD2 is involved in liver metabolism homeostasis, its exact role and molecular mechanisms remain largely undefined. The involvement of CRELD2 in liver metabolism was first reported by Nohara et al. Their results showed that gestational arsenic exposure significantly increased Creld2 expression in the liver of adult male offspring mice, accompanied by an increase in intracellular triglyceride accumulation in the liver (117). Subsequent studies further found that intraperitoneal administration of Tm for 24 h drastically induced CRELD2 protein expression in mouse livers (73). Moreover, in older Grp78 ^-/- mice, increased effects of alcohol on the methylation of CpG islands in the promoter regions of genes involved in ERAD, including Creld2, were detected (95). However, a direct causal link between CRELD2 and liver disease has not been demonstrated in these studies.

Through intensive studies on mouse models and human samples, Kern et al. recently revealed that CRELD2 plays a critical role in liver homeostasis (94). They generated a Creld2 knockout (Creld2 ^-/-) mouse model to investigate CRELD2 function in vivo (94). Their results showed that Creld2 ^-/- mice exhibited a reduction in body weight under both a chow diet and high-fat diet (HFD) compared to their controls but developed insulin resistance. Additionally, Creld2 ^-/- livers generally contained fewer lipids, which could account for lower body weight. Notably, their results clearly showed that 12 weeks of HFD did not induce ER stress in the liver, and neither transcriptome nor protein expression analysis revealed a lipid-driven ER stress response in the livers of Creld2 ^-/- mice. Moreover, this study revealed that the adipose weights of Creld2 ^-/- mice were significantly reduced (94). Another study also identified several genes, including Creld2, that were associated with feed efficiency using RNA sequencing in rumen papillae from steers (118). All these results suggest that CRELD2 plays a role in regulating whole-body energy balance, which remains elusive and warrants further investigation. To test whether CRELD2 is involved in the resolution of ER stress in the liver, Creld2 ^-/- mice and littermate controls were intraperitoneally injected with Tm or vehicle. Inducing ER stress via Tm administration exacerbated ER stress in Creld2 ^-/- mice, as indicated by upregulated GRP78 expression, and consequently increased hepatic lipid storage. Mechanistic studies have revealed that CRELD2 interacts with several chaperones and enzymes whose activity is required to overcome cellular stress, including GRP78, thioredoxin domain-containing 5, and glutathione S-transferase Mu2 (94, 119). These data further support the hypothesis that CRELD2 is involved in ER stress and the UPR, and CRELD2 function is required to maintain hepatic homeostasis under ER stress responses in mice.

Additionally, Kern et al. investigated whether human CRELD2 plays a role in the pathophysiological conditions of the liver. They found sex dimorphism in the expression levels of CRELD2 in the human liver, where both the mRNA and protein levels of CRELD2 were significantly upregulated in male patients with non-alcoholic steatohepatitis (NASH); however, expression in female patients remained unaffected (94). Notably, control patients showed expression similar to that of patients with simple steatosis. Furthermore, they found an inverse correlation between serum concentrations of CRELD2 and Steatosis, Activity, and Fibrosis (SAF) scores in male patients (94). These results indicate that CRELD2 exhibits a sex-specific function during NAFLD in humans, and upregulated CRELD2 expression in the liver is likely associated with a decrease in serum CRELD2 concentration, which is presumably associated with progression to NASH in male patients. Similarly, a sex dimorphism was also observed in aged mice, with only Creld2 ^-/- males developing steatosis (94). Based on the results obtained from both mouse models and human samples, CRELD2 likely plays an essential role in liver metabolic homeostasis; however, further studies are warranted to validate this.

ER stress reportedly involves in the pathogenesis of CVDs, including hypertension, atherosclerosis, heart failure, and myocardial atrophy (6, 12). In primary neonatal rat cardiomyocytes, Tm treatment significantly induced the mRNA expression of Creld2, accompanied by other UPR genes, and this upregulation was remarkably reversed by treatment with salubrinal, which is an ER stress inhibitor (71). Further studies revealed high expression of CRELD2 and other ER stress-related markers in human aneurysmal samples (96). This is accompanied by exacerbated apoptosis, high reactive oxygen species production, and a reduction in mitochondrial biogenesis in the vascular wall of abdominal aortic aneurysm, a degenerative vascular disease with a complex etiology (96). Marfan syndrome (MFS) is associated with mutations in the protein fibrillin-1 (FBN1), which affects the integrity of connective tissue elastic fibers. The most severe clinical outcome of MFS is cardiovascular system abnormalities characterized by progressive aortic root enlargement and ascending aortic aneurysm (97, 120, 121). Siegert et al. found a nearly undescribed FBN1 3’UTR mutation accompanied by a well-defined gene ontological ER stress response in the non-dilated aortic zone, which was confirmed by the increased expression of MANF, GRP78, and CRELD2 (97). These results indicate that CRELD2 is associated with CVD pathogenesis. However, comprehensively elucidating the roles and mechanisms of CRELD2 in CVDs using various animal and cell models is necessary.

ER stress is also implicated in the disturbance of cartilage and bone metabolism (60, 61, 122, 123). In vitro and in vivo studies demonstrate that CRELD2 plays an important role in these processes. The association between CRELD2 and cartilage metabolism was first reported by Rajpar et al. (98). They revealed that Creld2 was the most highly upregulated gene in chondrocytes from a Matn3 mutant model of multiple epiphyseal dysplasia (MED), which is a clinically variable and genetically heterogeneous chondrodysplasia characterized by mild short stature, joint pain, and stiffness and early onset osteoarthritis (98). Further studies have also revealed that CRELD2 expression in the hypertrophic zones of ER stress-related growth plate disease mouse models (Schmid and Cog) is significantly upregulated (99). Notably, MED, Schmid, and Cog are characterized by prolonged ER stress. These data also revealed that the protein levels of CRELD2 were upregulated in cell and mouse models of chondrodysplasia caused by mutations in Matn3 or Col10a1, but not in cartilage oligomeric matrix protein (Comp) (16). Notably, upon ER stress induced by matn3 mutation in vitro and in vivo, CRELD2 was also secreted into the ECM (16). Moreover, substrate-trapping experiments confirmed that PDI-like activity enabled CRELD2 to interact with several substrates, including MATN3, laminin 5 β3, type VI collagen, and thrombospondin 1 (16). Additionally, new elements of ER stress in IL-1α-treated cartilage reportedly involve Creld2 (100), further supporting that CRELD2 might be associated with cartilage homeostasis.

Additionally, CRELD2 participates in bone development and homeostasis. For example, Creld2 is among the top upregulated genes in bone morphogenetic protein 9 (BMP9)-stimulated osteogenic differentiation of mesenchymal stem cells (101). ChIP assays revealed that SMAD1/5/8 directly binds to the Creld2 promoter in a BMP9-dependent manner. Moreover, both in vitro and in vivo studies have revealed that exogenous Creld2 promotes BMP9-induced bone formation and matrix mineralization; conversely, silencing Creld2 expression suppresses BMP9-induced osteogenic differentiation (101). These results confirmed that CRELD2 plays an important role in BMP9-induced terminal osteogenic differentiation, although the specific mechanism still needs to be thoroughly investigated (101). Dennis et al. recently found that mice with cartilage-specific deletion of Creld2 had a chondrodysplasia-like phenotype with abnormal cartilage growth plates; however, the deletion of Creld2 in bone results in osteopenia, with a low bone density and altered trabecular architecture (102). Mechanistically, CRELD2, which possesses PDI-like activity, acts as a novel chaperone for LRP1, promoting its transport to the cell surface and subsequently modulating WNT signaling during the differentiation and maturation of chondrocytes and osteoblasts (102). They recently further revealed the critical role of CRELD2 in osteoclast differentiation (103). CRELD2 expression was significantly downregulated following osteoclastogenic differentiation in both the RAW264.7 cell line and mouse primary osteoclast precursors, and the overexpression of Creld2 impaired osteoclast differentiation in vitro. Mechanistic analysis revealed that CRELD2 expression blocks calcium release from the ER. This impairs osteoclast differentiation due to reduced calcium-dependent calcineurin activity and nuclear translocation of nuclear factor of activated T cells 1 (NFATc1), a master regulator of osteoclastogenesis (103). Interestingly, another study has shown that the first member of the CRELD family of proteins, CRELD1, promotes NFATc1 dephosphorylation and its subsequent nuclear translocation by directly binding to and modulating calcineurin activity (29, 31). The opposite effect on NFATc1 translocation mediated by CRELD1 and CRELD2 indicates that these two proteins fulfill distinct cellular functions, possibly due to their structural differences. As for CRELD2, conducting in vivo studies in animal models and clinical studies in humans is necessary, as these comprehensive studies could broaden our understanding of the critical role of CRELD2 in skeletal and other human diseases.

Increasing evidence has established that ER stress and UPR pathways play essential roles in tumor progression and survival (1, 6, 124). As a novel ER stress-responsive gene, Creld2 is highly correlated with cancer development, although the detailed underlying pathophysiology remains unclear. For example, in vitro studies revealed that CRELD2 expression significantly increased MB114 cell invasion and promoted a trend toward enhanced angiogenic sprouting, thereby suggesting that CRELD2 might be a mediator of tumor angiogenesis (104). Additionally, CRELD2 was reported as a novel androgen receptor target in prostate cancer (105). Yamada et al. identified 16 putative oncogenic targets of miR-451a regulation in renal cell carcinoma. Among these, CRELD2 was one of the target genes whose expression was significantly associated with poor prognosis in patients with renal cell carcinoma by TCGA database analyses (106). Additionally, CRELD2 gene and protein expressions are significantly upregulated in hepatocellular carcinoma (HCC) than in non-tumor tissues, and CRELD2 is associated with poor overall survival and disease-free survival in HCC (107). However, the specific role of CRELD2 in carcinogenesis remains unelucidated.

Sarah et al. recently established a causal link between CRELD2 and cancer (108). Their results showed that CRELD2 is a paracrine factor that underlines PERK-mediated cancer-associated fibroblast education downstream of Rho-associated kinase (ROCK) via an analysis of tumors from patients and mice (108). They found that Creld2 is regulated by PERK-modulated ATF4 via a putative C/ebp-Atf response element (CARE) in the promoter sequences of Creld2, and CRELD2 depletion suppresses tumor progression, indicating that the paracrine ROCK-PERK-ATF4-CRELD2 axis promotes breast cancer progression. They also revealed that high CRELD2 expression was associated with progressive human breast cancer (108). Therefore, these results establish that CRELD2 is a driver of tumor progression, and targeting CRELD2 may be a suitable anticancer therapy.

The observation that CRELD2 is secreted under increased ER stress suggests that it may be exploited as a soluble extracellular biomarker of ER stress-related diseases. Emerging evidence has characterized CRELD2 as a biomarker in human body fluids for molecular phenotyping of pathogenetic processes. For example, synovial fluid CRELD2 has been identified as a potential biomarker for prosthetic joint infection (109). Moreover, male NASH patients showed an inverse correlation between serum CRELD2 concentration and NASH progression, with low CRELD2 levels at high SAF scores (94).

Moreover, CRELD2 is characterized as an early, sensitive, non-invasive, and mechanistic biomarker in the urine in various ER stress-mediated kidney diseases, including hereditary NS, ischemic AKI, and autosomal dominant tubulointerstitial kidney disease (ADTKD), due to mutations in the UMOD gene encoding uromodulin (72, 125–127). In a podocyte ER stress-induced NS mouse model, CRELD2 cellular secretion and urinary excretion coincided with podocyte ER stress during the development of proteinuria and could be detected at an early stage of the disease. Moreover, tubular cell ER stress increases urinary CRELD2 excretion prior to subsequent decline in kidney function or histologic changes due to ER stress-induced AKI. Therefore, urinary CRELD2 excretion can serve as a mechanistic biomarker for ER-stressed tubular cells in the early phase of I/R-induced AKI (72). Additionally, these data have shown that early postoperative urinary CRELD2 elevation is significantly associated with severe AKI and other adverse outcomes following pediatric cardiac surgery. Urinary CRELD2 can be used to distinguish between controls and patients with early kidney disease (72). These data suggest that CRELD2 may be a promising ER stress biomarker with potential application in early diagnosis, risk stratification, treatment response monitoring, and guiding the development of ER stress modulators in targeted patient groups. Nevertheless, further clinical studies in a multi-institutional setting with a larger patient cohort are warranted. Notably, a recent immunohistochemical study on human fetal and postnatal human kidney samples revealed a high expression of CRELD2 in kidney structures during normal human fetal and postnatal kidney development (110). This implies that CRELD2 may play an essential role in kidney homeostasis, which also warrants further investigation.