Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
RSC Adv
2021 Aug 09;1143:27074-27083. doi: 10.1039/d1ra03156b.
Show Gene links
Show Anatomy links
Chemical characterization of red cells from the black sea urchin Arbacia lixula by X-ray photoelectron spectroscopy.
Pagliara P
,
Chirizzi D
,
Guascito MR
.
Abstract
Red spherula cells (RSC) from sea urchin coelomic fluid have attracted great interest for their specific and intriguing properties, such as for example antimicrobial activities and immune response, that probably tie in with their red characteristic pigments. Although to date different studies have been reported aimed to chemically characterize their pigments extracted from the cells, few data are available about the chemical characterization of the cell surface. In this work, a systematic chemical characterization of the RSC surface by X-ray photoelectron spectroscopy (XPS) analysis is described. The results were compared with data on colorless cells from the same coelomic fluid sample. Our observations evidenced that the two cell types were characterized by the presence of different chemical functional groups. In particular, the colorless cells are dominated by the presence of alkyl, alcohol, amide, and carboxyl groups in accordance with other similar cell types, enriched in Na+ and Cl- ions. Traces of elements like S (sulphonates) and P (phosphates) are also present. On the other hand, the RSC in addition to the alkyl groups show a reduction in the content of amide groups, accompanied by the anomalous presence of keto-enolic groups that probably can be associated with the presence of quinones/hydro-quinones from red pigments. A chemical enrichment in elements such as Cl- and Mg2+ and sulphate groups (-R-O-SO3 -), as well as the presence of sulphides and phosphates traces, is evident. The absence of carbonate groups is also observed in both cell populations, confirming the absence of sodium and magnesium carbonate salts. No traces of toxic elements (i.e., heavy metals) have been revealed.
Fig. 1. Cells from the sea urchin A. lixula. (a) Whole coelomic fluid with different cell types. (b) Cell population separation by a density gradient. (c) Colorless cells from P1. (d) Red cells from P4.
Fig. 2. Survey XPS spectra for colorless (A) and red (B) cells samples. Staked curves have been obtained by shifting red cells original counts along the Y-axis of a constant value of 700000 cps. As obtained original data can be appreciated in Fig. S4.†
Fig. 3. Atomic percentage composition (at%) of colorless and red cell surfaces. All data are representative of three averaged different analysed randomly selected samples spots. Reported errors represent the standard errors obtained from the variability observed on these three sample spots. * represent values near the limit of detection (LOD).
Fig. 4. XPS high-resolution region of C 1s (panels A and B), N 1s (panels C and D) and O 1s (panels E and F) for colorless and red cells, respectively.
Fig. 5. XPS high-resolution region of Cl 2p (panels A and B), Na 1s (panel C, no fit) and Mg1s (panel D, no fit) for colorless and red cells, respectively.
Fig. 6. XPS high-resolution region of S 2p (panel A, no-fit) and P 2p (panel B, no fit) for colorless and red cells.
Byrne,
Warming influences Mg2+ content, while warming and acidification influence calcification and test strength of a sea urchin.
2014, Pubmed,
Echinobase
Byrne,
Warming influences Mg2+ content, while warming and acidification influence calcification and test strength of a sea urchin.
2014,
Pubmed
,
Echinobase
Coates,
Echinochrome A Release by Red Spherule Cells Is an Iron-Withholding Strategy of Sea Urchin Innate Immunity.
2018,
Pubmed
,
Echinobase
Coffaro,
Immune response in the sea urchin Lytechinus pictus.
1977,
Pubmed
,
Echinobase
Fleutot,
Intercalation and grafting of benzene derivatives into zinc-aluminum and copper-chromium layered double hydroxide hosts: an XPS monitoring study.
2011,
Pubmed
Haug,
Antibacterial activity in Strongylocentrotus droebachiensis (Echinoidea), Cucumaria frondosa (Holothuroidea), and Asterias rubens (Asteroidea).
2002,
Pubmed
,
Echinobase
Heatfield,
Ultrastructural studies of regenerating spines of the sea urchin Strongylocentrotus purpuratus. II. Cell types with spherules.
1975,
Pubmed
,
Echinobase
Hira,
Autofluorescence mediated red spherulocyte sorting provides insights into the source of spinochromes in sea urchins.
2020,
Pubmed
,
Echinobase
Johnson,
The coelomic elements of sea urchins (Strongylocentrotus). 3. In vitro reaction to bacteria.
1969,
Pubmed
,
Echinobase
Johnson,
Comparative studies on the in vitro response of bacteria to invertebrate body fluids. I. Dendrostomum zostericolum, a sipunculid worm.
1970,
Pubmed
Pinsino,
Sea urchin coelomocytes as a novel cellular biosensor of environmental stress: a field study in the Tremiti Island Marine Protected Area, Southern Adriatic Sea, Italy.
2008,
Pubmed
,
Echinobase
Ploux,
Opposite responses of cells and bacteria to micro/nanopatterned surfaces prepared by pulsed plasma polymerization and UV-irradiation.
2009,
Pubmed
Russo,
Ovothiol isolated from sea urchin oocytes induces autophagy in the Hep-G2 cell line.
2014,
Pubmed
,
Echinobase
Skallberg,
Imaging XPS and photoemission electron microscopy; surface chemical mapping and blood cell visualization.
2017,
Pubmed
Zubavichus,
X-ray absorption spectroscopy of the nucleotide bases at the carbon, nitrogen, and oxygen K-edges.
2008,
Pubmed
de Faria,
Innate immune response in the sea urchin Echinometra lucunter (Echinodermata).
2008,
Pubmed
,
Echinobase