Abstract
Ceramide-1-phosphate (C1P) is a potential signaling molecule that modulates various cellular functions in animals. It has been known that C1P with different N-acyl lengths induce biological responses differently. However, molecular species profiles of the C1P in animal tissues have not been extensively examined yet. Here, we developed a method for determination of the molecular species of a C1P using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry with Phos-tag, a phosphate capture molecule. The amounts of total C1P in skin, brain, liver, kidney and small intestine of mice were determined to be 344, 151, 198, 96 and 90 pmol/g wet weight, respectively. We found a C1P species having an α-hydroxypalmitoyl residue (h-C1P, 44 pmol/g wet weight) in mouse skin. The h-C1P was detected only in the skin, and not other tissues of mice. The same analysis was applied to sphingomyelin after conversion of sphingomyelin to C1P by Streptomyces chromofuscus phospholipase D. We found that molecular species profiles of sphingomyelin in skin, kidney and small intestine of mice were similar to those of C1P in corresponding tissues. In contrast, molecular species profiles of sphingomyelin in liver and brain were quite different from those of C1P in these tissues, indicating selective synthesis or degradation of C1P in these tissues. The method described here will be useful for detection of changes in molecular species profiles of C1P and sphingomyelin.
This is a preview of subscription content, access via your institution.



Abbreviations
- C1P:
-
Ceramide-1-phosphate
- h-C1P:
-
C1P with 2-hydroxyl fatty acyl residue
- LCB:
-
Long-chain base
- lysoPtdOH:
-
Lysophosphatidic acid
- MALDI-TOF MS:
-
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
- PC1P:
-
Phytoceramide-1-phosphate
- PLD:
-
Phospholipase D
- PtdCho:
-
Phosphatidylcholine
- S1P:
-
Sphingosine-1-phosphate
- THAP:
-
2,4,6-Trihydroxyacetophenone
References
Pruett ST, Bushnev A, Hagedorn K, Adiga M, Haynes CA, Sullards MC, Liotta DC, Merrill AH Jr (2008) Biodiversity of sphingoid bases (sphingosines) and related amino alcohols. J Lipid Res 49:1621–1639
Masukawa Y, Narita H, Sato H, Naoe A, Kondo N, Sugai Y, Oba T, Homma R, Ishikawa J, Takagi Y, Kitahara T (2009) Comprehensive quantification of ceramide species in human stratum corneum. J Lipid Res 50:1708–1719
Hill JR, Wertz PW (2009) Structures of the ceramides from porcine palatal stratum corneum. Lipids 44:291–295
Iwamori M, Costello C, Moser HW (1979) Analysis and quantitation of free ceramide containing nonhydroxy and 2-hydroxy fatty acids, and phytosphingosine by high-performance liquid chromatography. J Lipid Res 20:86–96
Kihara A, Mitsutake S, Mizutani Y, Igarashi Y (2007) Metabolism and biological functions of two phosphorylated sphingolipids, sphingosine 1-phosphate and ceramide 1-phosphate. Prog Lipid Res 46:126–144
Kitano Y, Iwamori Y, Kiguchi K, DiGiovanni J, Takahashi T, Kasama K, Niwa T, Harii K, Iwamori M (1996) Selective reduction in α-hydroxypalmitic acid-containing sphingomyelin and concurrent increase in hydroxylated ceramides in murine skin tumors induced by an initiation-promotion regimen. Jpn J Cancer Res 87:437–441
Uchida Y, Hara M, Nishio H, Sidransky E, Inoue S, Otsuka F, Suzuki A, Elias PM, Holleran WM, Hamanaka S (2000) Epidermal sphingomyelins are precursors for selected stratum corneum ceramides. J Lipid Res 41:2071–2082
Breimer ME (1975) Distribution of molecular species of sphingomyelins in different parts of bovine digestive tract. J Lipid Res 16:189–194
Yasugi E, Kasama T, Seyama Y (1991) Composition of long chain bases in ceramide of the guinea pig Harderian gland. J Biochem 110:202–206
Hannun YA, Obeid LM (2008) Principles of bioactive lipid signalling: lessons from sphingolipids. Nat Rev Mol Cell Biol 9:139–150
Hannun YA, Obeid LM (2011) Many ceramides. J Biol Chem 286:27855–27862
Bornancin F (2011) Ceramide kinase: the first decade. Cell Signal 23:999–1008
Hoeferlin LA, Wijesinghe DS, Chalfant CE (2013) The role of ceramide-1-phosphate in biological functions. Sphingolipids: basic science and drug development. In: Gulbins E, Petrache I (eds) Handbook of experimental pharmacology. Springer, New York
Pettus BJ, Bielawska A, Subramanian P, Wijesinghe DS, Maceyka M, Leslie CC, Evans JH, Freiberg J, Roddy P, Hannun YA, Chalfant CE (2004) Ceramide 1-phosphate is a direct activator of cytosolic phospholipase A2. J Biol Chem 279:11320–11326
Subramanian P, Stahelin RV, Szulc Z, Bielawska A, Cho W, Chalfant CE (2005) Ceramide 1-phosphate acts as a positive allosteric activator of group IVA cytosolic phospholipase A2α and enhances the interaction of the enzyme with phosphatidylcholine. J Biol Chem 280:17601–17607
Wijesinghe DS, Subramanian P, Lamour NF, Gentile LB, Granado MH, Bielawska A, Szulc Z, Gòmez-Muñoz A, Chalfant CE (2009) Chain length specificity for activation of cPLA2α by C1P: use of the dodecane delivery system to determine lipid-specific effects. J Lipid Res 50:1986–1995
Gòmez-Muñoz A, Kong JY, Salh B, Steinbrecher UP (2004) Ceramide-1-phosphate blocks apoptosis through inhibition of acid sphingomyelinase in macrophages. J Lipid Res 45:99–105
Gòmez-Muñoz A, Kong JY, Parhar K, Wang SW, Gangoiti P, Gonzalez M, Eivemark S, Salh B, Duronio V, Steinbrecher UP (2005) Ceramide-1-phosphate promotes cell survival through activation of the phosphatidylinositol 3-kinase/protein kinase B pathway. FEBS Lett 579:3744–3750
Gòmez-Muñoz A, Frago LM, Alvarez L, Varela-Nieto I (1997) Stimulation of DNA synthesis by natural ceramide 1-phosphate. Biochem J 325:435–440
Mitra P, Maceyka M, Payne SG, Lamour N, Milstien S, Chalfant CE, Spiegel S (2007) Ceramide kinase regulates growth and survival of A549 human lung adenocarcinoma cells. FEBS Lett 581:735–740
Gangoiti P, Bernacchioni C, Donati C, Cencetti F, Ouro A, Gòmez-Muñoz A, Bruni P (2012) Ceramide 1-phosphate stimulates proliferation of C2C12 myoblasts. Biochemie 94:597–607
Kim TJ, Kang YJ, Lim Y, Lee HW, Bae K, Lee YS, Yoo JM, Yoo HS, Yun YP (2011) Ceramide 1-phosphate induces neointimal formation via cell proliferation and cell cycle progression upstream of ERK1/2 in vascular smooth muscle cells. Exp Cell Res 317:2041–2051
Granado MH, Gangoiti P, Ouro A, Arana L, Gonzalez M, Trueba M, Gòmez-Muñoz A (2009) Ceramide 1- phosphate (C1P) promotes cell migration involvement of a specific C1P receptor. Cell Signal 21:405–412
Kim C, Schneider G, Abdel-Latif A, Mierzejewska K, Sunkara M, Borkowska S, Ratajczak J, Morris AJ, Kucia M, Ratajczak MZ (2013) Ceramide-1-phosphate regulates migration of multipotent stromal cells and endothelial progenitor cells—implications for tissue regeneration. Stem Cells 31:500–510
Hankins JL, Ward KE, Linton SS, Barth BM, Stahelin RV, Fox TE, Kester M (2013) Ceramide-1-phosphate mediates endothelial cell invasion via the annexin a2-p11 heterotetrameric protein complex. J Biol Chem 288:19726–19738
Schneider G, Bryndza E, Abdel-Latif A, Ratajczak J, Maj M, Tarnowski M, Klyachkin Y, Houghton P, Morris AJ, Vater A, Klussmann S, Kucia M, Ratajczak MZ (2013) Bioactive lipids S1P and C1P are prometastatic factors in human rhabdomyosarcoma, and their tissue levels increase in response to radio/chemotherapy. Mol Cancer Res 11:793–807
Mitsutake S, Yokose U, Kato M, Matsuoka I, Yoo JM, Kim TJ, Yoo HS, Fujimoto K, Ando Y, Sugiura M, Kohama T, Igarashi Y (2007) The generation and behavioral analysis of ceramide kinase-null mice, indicating a function in cerebellar Purkinje cells. Biochem Biophys Res Commun 363:519–524
Graf C, Zemann B, Rovina P, Urtz N, Schanzer A, Reuschel R, Mechtcheriakova D, Müller M, Fischer E, Reichel C, Huber S, Dawson J, Meingassner JG, Billich A, Niwa S, Badegruber R, Van Veldhoven PP, Kinzel B, Baumruker T, Bornancin F (2008) Neutropenia with impaired immune response to Streptococcus pneumoniae in ceramide kinase-deficient mice. J Immunol 180:3457–3466
Niwa S, Graf C, Bornancin F (2009) Ceramide kinase deficiency impairs microendothelial cell angiogenesis in vitro. Microvasc Res 77:389–393
Wijesinghe DS, Brentnall M, Mietla JA, Hoeferlin LA, Diegelmann RF, Boise LH, Chalfant CE (2014) Ceramide kinase is required for a normal eicosanoid response and the subsequent orderly migration of fibroblasts. J Lipid Res 55:1298–1309
Simanshu DK, Kamlekar RK, Wijesinghe DS, Zou X, Zhai X, Mishra SK, Molotkovsky JG, Malinina L, Hinchcliffe EH, Chalfant CE, Brown RE, Patel DJ (2013) Non-vesicular trafficking by a ceramide-1-phosphate transfer protein regulates eicosanoids. Nature 500:463–467
Tanaka T, Tsutsui H, Hirano K, Koike T, Tokumura A, Satouchi K (2004) Quantitative analysis of lysophosphatidic acid by time-of-flight mass spectrometry using a phosphate-capture molecule. J Lipid Res 45:2145–2150
Morishige J, Urikura M, Takagi H, Hirano K, Koike T, Tanaka T, Satouchi K (2010) A clean-up technology for the simultaneous determination of lysophosphatidic acid and sphingosine-1-phosphate by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using a phosphate-capture molecule Phos-tag. Rapid Commun Mass Spectrom 24:1075–1084
Kinoshita E, Takahashi M, Takeda H, Shiro M, Koike T (2004) Recognition of phosphate monoester dianion by an alkoxide-bridged dinuclear zinc (II) complex. Dalton Trans 8:1189–1193
Tanaka T, Kida T, Imai H, Morishige J, Yamashita R, Matsuoka H, Uozumi S, Satoushi K, Nagano M, Tokumura A (2013) Identification of a sphingolipid-specific phospholipase D activity associated with the generation of phytoceramide-1-phosphate in cabbage leaves. FEBS J 280:3797–3809
Bligh EG, Dyer WJ (1959) A rapid method of total lipid extraction and purification. Can J Biochem Physiol 37:911–917
Chalvardjian A, Rudnicki E (1970) Determination of lipid phosphorus in the nanomolar range. Anal Biochem 36:225–230
Imai H, Yamamoto K, Shibahara A, Miyatani S, Nakayama T (2000) Determining double-bond positions in monoenoic 2-hydroxy fatty acid of glucosylceramides by gas chromatography-mass spectrometry. Lipids 35:233–236
Rouser G, Feldman G, Galli C (1965) Fatty acid compositions of human brain lecithin and sphingomyelin in normal individuals, senile cerebral cortical atrophy, Alzheimer’s disease, metachromatic leucodystrophy, Tay-Sachs and Niemann-Pick diseases. J Am Oil Chem Soc 42:411–412
O’Brien JS, Rouser G (1964) The fatty acid composition of brain sphingolipids: sphingomyelin, ceramide, cerebroside, and cerebroside sulfate. J Lipid Res 5:339–342
Imamura S, Horiuti Y (1979) Purification of Streptomyces chromofuscus phospholipase D by hydrophobic affinity chromatography on palmitoyl cellulose. J Biochem 85:79–95
Kruer MC, Paisan-Ruiz C, Boddaert N, Yoon MY, Hama H, Gregory A, Malandrini A, Woltjer RL, Munnich A, Gobin S, Polster BJ, Palmeri S, Edvardson S, Hardy J, Houldren H, Hayflick SJ (2010) Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA). Ann Neurol 68:611–618
Acknowledgments
This work was partly supported by grants-in-aid from the Ministry of Education, Science, Sports, and Culture of Japan (24580185), and the research program for development of an intelligent Tokushima artificial exosome (iTEX) from Tokushima University.
Author information
Authors and Affiliations
Corresponding author
About this article
Cite this article
Yamashita, R., Tabata, Y., Iga, E. et al. Analysis of Molecular Species Profiles of Ceramide-1-phosphate and Sphingomyelin Using MALDI-TOF Mass Spectrometry. Lipids 51, 263–270 (2016). https://doi.org/10.1007/s11745-015-4082-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11745-015-4082-0
Keywords
- Ceramide-1-phosphate
- Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
- Sphingomyelin
- Molecular species